US20040234516A1 - Production of lysosomal enzymes in plants by transient expression - Google Patents

Production of lysosomal enzymes in plants by transient expression Download PDF

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US20040234516A1
US20040234516A1 US10/851,388 US85138804A US2004234516A1 US 20040234516 A1 US20040234516 A1 US 20040234516A1 US 85138804 A US85138804 A US 85138804A US 2004234516 A1 US2004234516 A1 US 2004234516A1
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Stephen Garger
Thomas Turpen
Monto Kumagai
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Large Scale Biology Corp
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Definitions

  • This invention is in the field of therapeutic peptides. Specifically this invention relates to the production of pharmaceutical peptides and proteins encoded on a recombinant plant virus or and produced by an infected plant or produced by a recombinant plant.
  • the present invention relates especially to the production of human and animal lysosomal enzymes in plants comprising expressing the genetic coding sequence of a human or animal lysosomal enzyme in a plant expression system.
  • the plant expression system provides for post-translational modification and processing to produce recombinant protein having enzymatic activity.
  • transgenic or transfected tobacco plants produce a modified human ⁇ galactosidase and a glucocerebrosidase, both of which are enzymatically active.
  • the recombinant lysosomal enzymes produced in accordance with the invention may be used for a variety of purposes including but not limited to enzyme replacement therapy for the therapeutic treatment of lysosomal storage diseases, research for development of new approaches to medical treatment of lysosomal storage diseases, and industrial processes involving enzymatic substrate hydrolysis.
  • Lysosomes which are present in all animal cells, are acidic cytoplasmic organelles that contain an assortment of hydrolytic enzymes. These enzymes function in the degradation of internalized and endogenous macromolecular substrates. When there is a lysosomal enzyme deficiency, the deficient enzyme's undegraded substrates gradually accumulate within the lysosomes causing a progressive increase in the size and number of these organelles within the cell. This accumulation within the cell eventually leads to malfunction of the organ and to the gross pathology of a lysosomal storage disease, with the particular disease depending on the particular enzyme deficiency. More than thirty distinct, inherited lysosomal storage diseases have been characterized in humans.
  • lysosomal storage diseases One proven treatment for lysosomal storage diseases is enzyme replacement therapy in which an active form of the enzyme is administered directly to the patient.
  • enzyme replacement therapy in which an active form of the enzyme is administered directly to the patient.
  • abundant, inexpensive and safe supplies of therapeutic lysosomal enzymes are not commercially available for the treatment of any of the lysosomal storage diseases.
  • metabolic storage disorders There are a large number of metabolic storage disorders known to affect man. As a group, these diseases are the most prevalent genetic abnormalities of humans, yet individually they are quite rare.
  • One of the three major classes of these conditions, comprising the majority of patients, is the sphingolipidoses in which excessive quantities of undegraded fatty components of cell membranes accumulate because of inherited deficiencies of specific catabolic enzymes.
  • Principal disorders in this category are Gaucher disease, Niemann-Pick disease, Fabry disease, and Tay-Sachs disease. All of these disorders are caused by harmful mutations in the genes that code for specific housekeeping enzymes within lysosomes.
  • enzyme replacement therapy requires that the requisite exogenous enzyme be taken up by the cells in which the materials are catabolized and that they be incorporated into lysosomes within these cells.
  • Fabry disease is an ideal candidate for enzyme replacement therapy because the disease does not involve the central nervous system. The therapeutic enzyme does not need to be delivered across the blood-brain barrier (1, 2).
  • the modified enzyme (alglucerase) is now produced commercially by Genzyme Corporation in Cambridge, Mass., under the trade name CeredaseTM. The beneficial effects of this treatment have been universally confirmed (11-13). Production of recombinant glucocerebrosidase (imiglucerase) is underway in Chinese hamster ovary (CHO) cells, and the product (CerezymeTM) is as effective as placental glucocerebrosidase (14). The experience with Gaucher treatment validates enzyme replacement therapy with a product that requires post-translational modifications.
  • Gal-A galactosidase A
  • Human Gal-A is a glycoprotein homodimer with a molecular weight of approximately 101 kDa containing 5-15% Asn-linked carbohydrate.
  • the enzyme contains approximately equal portions of high mannose and complex type glycans. Upon isoelectric focusing, many forms of the enzyme are observed due to differences in sialylation depending on the source of the protein (tissue or plasma forms).
  • the disease is inherited as an X-linked recessive trait. A number of specific mutations in the gene have been characterized, including partial rearrangements, splice-junction defects and point mutations.
  • the two “isozymes” were separable by electrophoresis, isoelectric focusing, and ion exchange chromatography. After neuraminidase treatment, the electrophoretic migrations and pI value of ⁇ -Gal A and B were similar (70), initially suggesting that the two enzymes were the differentially glycosylated products of the same gene.
  • the finding that the purified glycoprotein enzymes had similar physical properties including subunit molecular weight (about 46 kDa), homodimeric structures, and amino acid compositions also indicated their structural relatedness (70. 71. 72. 73. 74. 75. 76. 77).
  • the administered enzyme not only depleted the substrate from the circulation (a major site of accumulation), but also possibly mobilized the previously stored substrate from other depots into the circulation for subsequent clearance.
  • ⁇ -Gal A human enzyme has a molecular weight of approximately 101,000 Da. On SDS gel electrophoresis it migrates as a single band of approximately 49,000 Da indicating the enzyme is a homodimer (Bishop & Desnick, 1981, J. Biol. Chem. 256: 1307).
  • ⁇ -Gal A is synthesized as a 50,500 Da precursor containing phosphorylated endoglycosidase H sensitive oligosaccharides. This precursor is processed to a mature form of about 46,000 Da within 3-7 days after its synthesis. The intermediates of this processing have not been defined (Lemansky, et al., 1987, J. Biol. Chem. 262:2062).
  • . ⁇ .-Gal A is targeted to the lysosome via the mannose-6-phosphate receptor. This is evidenced by the high secretion rate of this enzyme in mucolipidosis II cells and in fibroblasts treated with NH.sub.4 Cl.
  • the enzyme has been shown to contain 5-15% Asn linked carbohydrate (Ledonne, et al., 1983, Arch. Biochem. Biophys. 224:186).
  • the tissue form of this enzyme was shown to have about 52% high mannose and 48% complex type oligosaccharides.
  • the high mannose type coeluted, on Bio-gel chromatography, with Man.sub.8-9 GlcNAc while the complex type oligosaccharides were of two categories containing 14 and 19-39 glucose units.
  • isoelectric focusing many forms of this enzyme are observed depending on the sources of the purified enzyme (tissue vs plasma form).
  • the human protein was expressed at low levels and could not be purified from the bacteria. These results indicate that the recombinant enzyme was unstable due to the lack of normal glycosylation and/or the presence of endogenous cytoplasmic or periplasmic proteases.
  • Gaucher disease is the most common lysosomal storage disease in humans, with the highest frequency encountered in the Ashkenazi Jewish population. About 5,000 to 10,000 people in the United States are afflicted with this disease (Grabowski, 1993, Adv. Hum. Genet. 21:377-441). Gaucher disease results from a deficiency in glucocerebrosidase (hGCB); glucosylceramidase; acid ⁇ -glucosidase; EC 3.2.1.45).
  • hGCB replacement therapy has revolutionized the medical care and management of Gaucher disease, leading to significant improvement in the quality of life of many Gaucher patients (Pastores et al., 1993, Blood 82:408-416; Fallet et al., 1992, Pediatr. Res. 31:496-502).
  • Studies have shown that regular, intravenous administration of specifically modified hGCB (Ceredase.TM., Genzyme Corp.) can result in dramatic improvements and even reversals in the hepatic, splenic and hematologic manifestations of the disease (Pastores et al., 1993, supra; Fallet: et al., 1992, supra; Figueroa et al., 1992, N. Eng. J.
  • hGCB replacement therapy Despite the benefits of hGCB replacement therapy, the source and high cost of the enzyme seriously restricts its availability. Until recently, the only commercial source of purified hGCB has been from pooled human placentae, where ten to twenty kilograms (kg) of placentae yield only 1 milligram (mg) of enzyme. From five hundred to two thousand kilograms of placenta (equivalent to 2,000-8,000 placentae) are required to treat each patient every two weeks. Current costs for hGCB replacement therapy range from $55 to $220/kg patient body weight every two weeks, or from $70,000 to $300,000/year for a 50 kg patient. Since the need for therapy essentially lasts for the duration of a patient's life, costs for the enzyme alone may exceed $15,000,000 during 30 to 70 years of therapy.
  • a second major problem associated with treating Gaucher patients with glucocerebrosidase isolated from human tissue (and perhaps even from other animal tissues) is the risk of exposing patients to infectious agents which may be present in the pooled placentae, e.g., human immuno-deficiency virus (HIV), hepatitis viruses, and others.
  • infectious agents e.g., human immuno-deficiency virus (HIV), hepatitis viruses, and others.
  • Hurler syndrome is the most common of the group of human lysosomal storage disorders known as the mucopolysaccharidosis (MPS) involving an inability to degrade dermatan sulfate and heparan sulfate.
  • MPS mucopolysaccharidosis
  • Hurler patients are deficient in the lysosomal enzyme, ⁇ -L-iduronidase (IDUA), and the resulting accumulation of glucosaminoglycans in the lysosomes of affected cells leads to a variety of clinical manifestations (Neufeld & Ash well, 1980, The Biochemistry of Glycoproteins and Proteoglycans, ed. W. J. Lennarz, Plenum Press, N.Y.; pp.
  • IDUA ⁇ -L-iduronidase
  • Lysosomal Enzymes Biosynthesis and Targeting
  • Lysosomal enzymes are synthesized on membrane-bound polysomes in the rough endoplasmic reticulum. Each protein is synthesized as a larger precursor containing a hydrophobic amino terminal signal peptide. This peptide interacts with a signal recognition particle, an 11S ribonucleoprotein, and thereby initiates the vectoral transport of the nascent protein across the endoplasmic reticulum membrane into the lumen (Erickson, et al., 1981, J. Biol. Chem. 256:11224; Erickson, et al., 1983, Biochem. Biophys. Res. Commun. 115:275; Rosenfeld, et al., 1982, J. Cell Biol.
  • Lysosomal enzymes are cotranslationally glycosylated by the en bloc transfer of a large preformed oligosaccharide, glucose-3, mannose-9, N-acetylglucosamine-2, from a lipid-linked intermediate to the Asn residue of a consensus sequence Asn-X-Ser/Thr in the nascent polypeptide (Kornfeld, R. & Kornfeld, S., 1985, Annu. Rev. Biochem. 54:631).
  • the signal peptide is cleaved, and the processing of the Asn-linked oligosaccharide begins by the excision of three glucose residues and one mannose from the oligosaccharide chain.
  • the proteins move via vesicular transport, to the Golgi stack where they undergo a variety of posttranslational modifications, and are sorted for proper targeting to specific destinations: lysosomes, secretion, plasma membrane.
  • lysosomes secretion
  • plasma membrane a membrane glycoprotein
  • the oligosaccharide chain on secretory and membrane glycoproteins is processed to the sialic acid-containing complex-type. While some of the oligosaccharide chains on lysosomal enzymes undergo similar processing, most undergo a different series of modifications. The most important modification is the acquisition of phosphomannosyl residues which serve as an essential component in the process of targeting these enzymes to the lysosome (Kaplan, et al., 1977, Proc. Natl.
  • N-acetylglucosaminyl-phosphotransferase transfers N-acetylglucosamine-1-phosphate from the nucleotide sugar uridine diphosphate-N-acetylglucosamine to selected mannose residues on lysosomal enzymes to give rise to a phosphodiester intermediate (Reitman & Kornfeld, 1981, J. Biol. Chem. 256:4275; Waheed, et al., 1982, J. Biol. Chem. 257:12322).
  • N-acetylglucosamine-1-phosphodiester ⁇ -N-acetylglucosaminidase removes N-acetylglucosarnine residue to expose the recognition signal, mannose-6-phosphate (Varki & Kornfeld, 1981, J. Biol. Chem. 256: 9937; Waheed, et al., 1981, J. Biol. Chem. 256:5717).
  • the lysosomal enzymes bind to mannose-6-phosphate (M-6-P) receptors in the Golgi. In this way the lysosomal enzymes remain intracellular and segregate from the proteins which are destined for secretion.
  • M-6-P mannose-6-phosphate
  • the ligand-receptor complex then exits the Golgi via a coated vesicle and is delivered to a prelysosomal staging area where dissociation of the ligand occurs by acidification of the compartment (Gonzalez-Noriega, et al., 1980, J. Cell Biol. 85: 839).
  • the receptor recycles back to the Golgi while the lysosomal enzymes are packaged into vesicles to form primary lysosomes. Approximately, 5-20% of the lysosomal enzymes do not traffic to the lysosomes and are secreted presumably, by default. A portion of these secreted enzymes may be recaptured by the M-6-P receptor found on the cell surface and be internalized and delivered to the lysosomes (Willingham, et al., 1981, Proc. Natl. Acad. Sci. USA 78:6967).
  • a 215 kDa glycoprotein has been purified from a variety of tissues (Sahagian, et al., 1981, Proc. Natl. Acad. Sci. USA, 78:4289; Steiner & Rome, 1982, Arch. Biochem. Biophys. 214:681). The binding of this receptor is divalent cation independent.
  • a second M-6-P receptor also has been isolated which differs from the 215 kDa receptor in that it has a requirement for divalent cations.
  • this receptor is called the cation-dependent (M-6-P.sup.CD) while the 215 kDa one is called cation-independent (M-6-P.sup.Cl).
  • M-6-P.sup.CD receptor appears to be an oligomer with three subunits with a subunit molecular weight of 46 kDa.
  • hGCB human glucocerebrosidase
  • hGCB is synthesized as a single polypeptide (58 kDa) with a signal sequence (2 kDa) at the amino terminus.
  • the signal sequence is co-translationally cleaved and the enzyme is glycosylated with a heterogeneous group of both complex and high-mannose oligosaccharides to form a precursor.
  • the glycans are predominately involved in protein conformation.
  • the “high mannose” precursor which has a molecular weight of 63 KDa, is post-translationally processed in the Golgi to a 66 KDa intermediate, which is then further modified in the lysosome to the mature enzyme having a molecular weight of 59 KDa (Jonsson et al., 1987, Eur. J. Biochem. 164:171; Erickson et al., 1985, J. Biol. Chem., 260:14319).
  • the mature hGCB polypeptide is composed of 497 amino acids and contains five N-glycosylation amino acid consensus sequences (Asn-X-Ser/Thr). Four of these sites are normally glycosylated. Glycosylation of the first site is essential for the production of active protein. Both high-mannose and complex oligosaccharide chains have been identified (Berg-Fussman et al., 1993, J. Biol. Chem. 268:14861-14866). hGCB from placenta contains 7% carbohydrate, 20% of which is of the high-mannose type (Grace & Grabowski, 1990, Biochem. Biophys. Res. Comm. 168:771-777).
  • placental hGCB Treatment of placental hGCB with neuraminidase (yielding an asialo enzyme) results in increased clearance and uptake rates by rat liver cells with a concomitant increase in hepatic enzymatic activity (Furbish et al., 1981, Biochim. Biophys. Acta 673:425-434).
  • This glycan-modified placental hGCB is currently used as a therapeutic agent in the treatment of Gaucher's disease.
  • Biochemical and site-directed mutagenesis studies have provided an initial map of regions and residues important to folding, activator interaction, and active site location (Grace et al., 1994, J. Biol. Chem. 269:2283-2291).
  • hGCB Active monomers of hGCB have been purified from insect cells (Sf9 cells) and Chinese hamster ovary (CHO) cells infected or transfected, respectively, with hGCB cDNA (Grace & Grabowski, 1990, supra; Grabowski et al., 1989, Enzyme 41:131-142).
  • plants are eukaryotes, plant expression systems have advantages over prokaryotic expression systems, particularly with respect to correct processing of eukaryotic gene products.
  • plant cells do not possess lysosomes.
  • the plant vacuole appears functionally analogous to the lysosome, plants do not contain MPRs (Chrispeels, 1991, Ann. Rev. Pl. Phys. Pl. Mol. Biol. 42:21-53; Chrispeels and Tague, 1991, Intl. Rev. Cytol. 125:1-45), and the mechanisms of vacuolar targeting can differ significantly from those of lysosomal targeting.
  • vacuolar targeting in plants does not appear to be glycan-dependent, but appears to be based instead on C— or N-terminal peptide sequences (Gomez & Chrispeels, 1993, Plant Cell 5:1113-1124; Chrispeels & Raikhal, 1992, Cell 68:613-618; Holwerda et al., 1992, Plant Cell 4:307-318; Neuhaus et al., 1991, Proc. Natl. Acad. Sci.
  • An object of this invention is to provide the existing patient population with enough active enzyme to develop a lower cost treatment.
  • the enzymatic, structural, and glycan compositional analyses show rGal to be active.
  • glycoprotein modification and drug delivery allow, as examples, the chemical conjugation of peptides to carbohydrate, the covalent addition of polyethylene glycol to enzymes and the liposomal encapsulation of protein.
  • Many additional new concepts can be tested to increase the half-life of enzymes in circulation and optimize cellular and subcellular targeting. Ideally, these modifications will require a facile and rapid genetic system to produce large quantities of highly pure enzyme and an effective animal disease model for drug development.
  • Our lab-scale process appears highly scalable and is capable of producing grams of enzyme per month in existing indoor greenhouse growth areas.
  • AA preproenzyme amino acid
  • the present invention provides for a polypeptide comprising (a) the complete, or a fragment of, the amino acid sequence of ⁇ -galactosidase with or without (b) an ER-retention signal, such as the amino acid sequence SEKDEL (SEQ ID NO:37), wherein the ER-retention signal is at the carboxy end of the complete, or a fragment of, the amino acid sequence of ⁇ -galactosidase, wherein said fragment of the amino acid sequence of ⁇ -galactosidase comprises a deletion of at the carboxy end of ⁇ -galactosidase, wherein said deletion is one to twenty-five amino acids.
  • the present invention also provides for a polynucleotide encoding the aforementioned polypeptide.
  • the present invention also relates to the production of these human or animal lysosomal enzymes, including the aforementioned polypeptides, in transformed or transfected plants, plant cells or plant tissues, and involves constructing and expressing recombinant expression constructs comprising lysosomal enzyme coding sequences in a plant expression system.
  • the plant expression system provides appropriate co-translational and post-translational modifications of the nascent peptide required for processing, e.g., signal sequence cleavage, glycosylation, and sorting of the expression product so that an enzymatically active protein is produced.
  • recombinant lysosomal enzymes are produced in plant expression systems from which the recombinant lysosomal enzymes can be isolated and used for a variety of purposes.
  • the present invention is exemplified by virally transfected and transgenic tobacco plants with lysosomal enzyme expression constructs.
  • One construct comprises a nucleotide sequence encoding a modified human glucocerebrosidase (hGCB).
  • Another construct comprises nucleotide sequence encoding a human ⁇ galactosidase ( ⁇ gal or ⁇ gal A).
  • hGCB modified human glucocerebrosidase
  • ⁇ gal or ⁇ gal A a human ⁇ galactosidase
  • Virally transfected and transgenic tobacco plants having the expression constructs produce lysosomal enzymes that are enzymatically active and have high specific activity.
  • the plant expression systems and the recombinant lysosomal enzymes produced therewith have a variety of uses, including but not limited to: (1) the production of enzymatically active lysosomal enzymes for the treatment of lysosomal storage diseases; (2) the production of altered or mutated proteins, enzymatically active or otherwise, to serve as precursors or substrates for further in vivo or in vitro processing to a specialized industrial form for research or therapeutic uses, such as to produce a more effective therapeutic enzyme; (3) the production of antibodies against lysosomal enzymes for medical diagnostic use; and (4) use in any commercial process that involves substrate hydrolysis.
  • FIG. 1 shows a Tobamovirus expression vectors.
  • FIG. 2 shows a Tobamovirus expression vector containing the human ax galactosidase gene or a variant of the gene.
  • the amino acid sequence of cCASP and Native SP depicted in FIG. 2 are depicted in SEQ ID. NO: 1 and 2, respectively.
  • the entire amino acid sequence of WT rGAL-A is depicted in SEQ ID NO: 4.
  • FIG. 3A shows accumulation by Western Analysis of total plant soluble extract anti human GAL-A sera.
  • FIG. 3B shows activity of WT rGAL-A at 8 and 14+ days post inoculation of the plant host with a viral vector.
  • FIG. 4A shows Western blot analysis of total plant soluble extract anti human GAL-A sera
  • FIG. 4B shows activity of WT rGAL-wt and rGAL-wtR at 8 and 14+ days post inoculation of the plant host with a viral vector.
  • FIG. 5 shows carboxy terminal modifications to ⁇ galactosidase.
  • the asterisk indicates a potential CTPP cleavage site according to Gene 58: 177, 1987.
  • the entire nucleic acid and amino acid sequences of WT RGAL-A, WT-rGAL-AR, rGAL-4, rGAL-4R, rGAL-8, rGAL-8R, rGAL-12, rGAL-12R, rGAL-25, and rGAL-25R are depicted in SEQ ID NO: 3-22, respectively.
  • FIG. 6 shows western blot analysis of the accumulation of 10 carboxy-modified rGAL-A variants from interstitial fluid and from total plant homogenate.
  • FIG. 7 shows a comparison of enzymatic activity of the 10 carboxy-modified RGAL-A variants.
  • FIG. 8 shows a Coomassie blue stained electrophoresis gel separation of carboxy-modified rGAL-A variants and controls.
  • FIG. 9 shows a Coomassie blue stained electrophoresis gel separation of carboxy-modified rGAL-A variants and controls.
  • FIG. 10 shows a schematic representation of rGAL-A secretion from the endoplasmic reticulum to the apoplast.
  • FIG. 11 shows different glycosylation structures of ⁇ galactosidase.
  • FIG. 12 shows TTODA (rGAL-12R) TMV RNA begins at base 1; 126/183 reading frame begins at 69, 3417 is suppressible stop codon, and ends at 4919.30K ORF begins at 4903 and ends at 5709.
  • Human a galactosidase A RNA begins at 5703, ⁇ amylase signal peptide is from 5762-5857; mature human ⁇ galactosidase A coding region is 5858-7036, ToMV virus coat protein and 3 UTR follows. (SEQ ID NO: 33)
  • FIG. 13 shows SBS5-rGAL-12R TMV RNA begins at base 1; 126/183 reading frame begins at 69, 3417 is suppressible stop codon, and ends at 4919.30K ORF begins at 4903 and ends at 5709.
  • Human ⁇ galactosidase A RNA begins at 5703, complete (signal peptide and mature protein coding region) human ⁇ galactosidase A gene 5766-7037, TMV U5 virus coat protein and 3 UTR follows (SEQ ID. NO: 34).
  • FIG. 14 shows the construct within pBSG638: a dual Cauliflower Mosiac Virus 35S promoter linked to a translational enhancer from Tobacco Etch Virus linked 5′ to, and a polyadenylation region from the nopline synthase gene of Agrobacterium tumefaciens linked 3′ to, the native human GCB cDNA.
  • FIG. 15 shows the construct within pBSG641: a dual Cauliflower Mosiac Virus 35S promoter linked 5′ to, and a polyadenylation region from the nopline synthase gene of Agrobacterium tumefaciens linked 3′ to, the entire genome of Tobacco Mosaic Virus except the coat protein region is replaced with the GCB gene.
  • the present invention provides a polynucleotide comprising the nucleotide sequence depicted in SEQ ID NO: 3, 5, 7, 9, 11, 13, 15, 17, 19, 31, or 32.
  • the present invention also provides a polypeptide comprising the amino acid sequence depicted in SEQ ID NO: 4, 6, 8, 10, 12, 14, 16, 18, or 20.
  • the present invention further provides for a polypeptide comprising (a) the complete, or a fragment of, the amino acid sequence of ⁇ -galactosidase and (b) the amino acid SEKEL (SEQ ID NO:37), wherein SEKEL is at the carboxy end of the complete, or a fragment of, the amino acid sequence of ⁇ -galactosidase, wherein said fragment of the amino acid sequence of ⁇ -galactosidase comprises a deletion of at the carbozy end of ⁇ -galactosidase, wherein said deletion is one to twenty-five amino acids.
  • the deletion is one to twelve amino acids. More preferably, the deletion is four to twelve amino acids.
  • the present invention further provides for a polynucleotide comprising a nucleotide sequence encoding the aforementioned polypeptide(s).
  • the present invention further provides for a polynucleotide encoding the aforementioned polypeptide(s).
  • the present invention also provides for a viral vector or expression vector comprising the aforementioned polynucleotide(s) or encoding the aforementioned polypeptide(s).
  • the viral vector or expression vector is capable of expression and systemic expression of the polypeptide(s) encoded by the polynucleotide in a plant cell or a plant.
  • the viral vector or expression vector is derived from or based on or obtained from an RNA virus or an RNA viral vector. More preferably, the RNA virus is an RNA plant virus. Even more preferably, the RNA plant virus is a single-stranded plus-sense RNA plant virus.
  • the RNA plant virus is multi-partite, monopartite, bipartite, tripartite, or the like. Even much more preferably, the single-stranded plus-sense RNA plant virus is a tobamovrius, such as a tobacco mosaic virus.
  • the present invention further provides for a plant cell or a plant expressing the aforementioned polypeptide(s).
  • the present invention provides for a method for producing a protein of choice comprising a lysosomal enzyme which is enzymatically active, comprising: recovering the lysosomal enzyme from (i) a transgenic plant cell or (ii) a cell, tissue or organ of a transgenic plant, which transgenic plant cell or plant is transformed or transfected with a recombinant expression construct comprising a nucleotide sequence encoding the lysosomal enzyme and a promoter that regulates expression of the nucleotide sequence so that the lysosomal enzyme is expressed by the transgenic plant cell or plant.
  • the promoter can be an inducible promoter.
  • the inducible promoter can be induced by mechanical gene activation.
  • the method can be carried out with the transgenic plant and additionally comprises a step of inducing the inducible promoter before or after the transgenic plant is harvested, which inducing step is carried out before recovering the lysosomal enzyme from the cell, tissue or organ of the transgenic plant.
  • the lysosomal enzyme can be a modified lysosomal enzyme which is enzymatically active and comprises: (a) an enzymatically-active fragment of a human or animal lysosomal enzyme; (b) the human or animal lysosomal enzyme or (a) having one or more amino acid residues added to the amino or carboxyl terminus of the human or animal lysosomal enzyme or (a); or (c) the human or animal lysosomal enzyme or (a) having one or more naturally-occurring amino acid additions, deletions or substitutions.
  • the modified lysosomal enzyme can comprise a signal peptide or detectable marker peptide at the amino or carboxyl terminal of the modified lysosomal enzyme.
  • the modified lysosomal enzyme can be recovered from (i) the transgenic plant cell or (ii) the cell, tissue or organ of the transgenic plant by reacting with an antibody that binds the detectable marker peptide.
  • the antibody can be a monoclonal antibody.
  • the modified lysosomal enzyme can comprise: (a) an enzymatically-active fragment of an a-N-acetylgalactosaminidise, acid lipase, a-galactosidase, glucocerebrosidase, a-L-iduronidase, iduronak sulfatase, a-mannosidase or sialidase; (b) the a-N-a-cetylgalactosaminidase, acid lipase, a-galactosidase, glucocerebrosidase, a-L-iduronidase, iduronate sulfatase, a-mannosidase, sialidase or (a) having one or more amino acid residues added to the amino or carboxyl terminus of the a-N-acetylgalactosaminidase, acid lipase, a-galactos
  • the modified lysosomal enzyme can comprise: (a) an enzymatically-active fragment of a human glucocerebrosidase or human ⁇ -L-iduronidase enzyme; (b) the human glucocerebrosidase, human ⁇ -L-iduronidase or (a) having one or more amino acid residues added to the amino or carboxyl terminus of the human glucocerebrosidase, human ⁇ -L-iduronidase or (a); or (c) the human glucocerebrosidase, human ⁇ -Liduronidase or (a) having one or more naturally-occurring amino acid additions, deletions or substitutions.
  • the modified lysosomal enzyme can be a fusion protein comprising: (I) (a) the enzymatically-active fragment of the human or animal lysosomal enzyme, (b) the human or animal lysosomal enzyme, or (c) the human or animal lysosomal enzyme or (a) having one or more naturally-occurring amino acid additions, deletions or substitutions, and (II) a cleavable linker fused to the amino or carboxyl terminus of (I); and the method comprises: (a) recovering the fusion protein from the transgenic plant cell, or the cell, tissue or organ of the transgenic plant; (b) treating the fusion protein with a substance that cleaves the cleavable linker so that (1) is separated from the cleavable linker and any sequence attached thereto; and (c) recovering the separated (I).
  • the transgenic plant can be a transgenic tobacco plant.
  • the lysosomal enzyme can be a human or animal lysosomal enzyme.
  • the lysosomal enzyme can be an ⁇ -N-cetylgalactosaminidase, acid lipase, ⁇ -galactosidase, glucocerebrosidase, ⁇ -L-iduronidase, iduronate sulfatase, ⁇ -mannosidase or sialidese.
  • the lysosomal enzyme can be a human glucocerebrosidase or human ⁇ -L-iduronidase.
  • the organ can be a leaf, stem, root, flower, fruit or seed.
  • the present invention provides for a recombinant expression construct comprising a nucleotide sequence encoding a protein of choice comprising a lysosomal enzyme and a promoter that regulates the expression of the nucleotide sequence in a plant cell.
  • the promoter can be an inducible promoter.
  • the inducible promoter can be induced by mechanical gene activation.
  • the lysosomal enzyme can be a modified lysosomal enzyme which is enzymatically active and comprises: (a) an enzymatically active fragment of a human or animal lysosomal enzyme; (b) the human or animal lysosomal enzyme or (a) having one or more amino acid residues added to the amino or carboxyl terminus of the human or animal lysosomal enzyme or (a); or (c) the human or animal lysosomal enzyme or (a) having one or more naturally-occurring amino acid additions, deletions or substitutions.
  • the modified lysosomal enzyme can comprise a signal peptide or detectable marker peptide at the amino or carboxyl terminal of the modified lysosomal enzyme.
  • the modified lysosomal enzyme can comprise (a) an enzymatically-active fragment of an ⁇ -N-acetylgalactosaminidase, acid lipase, ⁇ -galactosidase, glucocerebrosidase, ⁇ -L-iduronidase, iduronate sulfatase, ⁇ -mannosidase or sialidase; (b) the ⁇ -N-acetylgalactosaminidase, acid lipase, ⁇ -galactosidase, glucocerebrosidase, ⁇ -L-iduronidase, iduronate sulfatase, ⁇ -mannosidase, sialidase or (a) having one or more amino acid residues added to the amino or carboxyl terminus of the ⁇ -N-acetylgalactosaminidase, acid lipase, ⁇ -galactosaminidas
  • the modified lysosomal enzyme can comprise (a) an enzymatically-active fragment of a human glucocerebrosidase or human ⁇ -L-iduronidase enzyme; (b) the human glucocerebrosidase or human ⁇ -L-iduronidase or (a) having one or more amino acid residues added to the amino or carboxyl terminus of the human glucocerebrosidase, human ⁇ -L-iduronidase or (a); or (c) the human glucocerebrosidase, human ( ⁇ -L-iduronidase or (a) having one or more naturally-occurring amino acid additions, deletions or substitutions.
  • the modified lysosomal enzyme can be a fusion protein comprising: (I) (a) the enzymatically-active fragment of the human or animal lysosomal enzyme, (b) the human or animal lysosomal enzyme, or (c) the human or animal lysosomal enzyme or (a) having one or more naturally-occurring amino acid additions, deletions or substitutions, and (II) a cleavable linker fused to the amino or carboxyl terminus of (I).
  • the lysosomal enzyme can be a human or animal lysosomal enzyme.
  • the lysosomal enzyme can be an ⁇ -N-acetylgalactosaminidase, acid lipase, ⁇ -galactosidase, glucocerebrosidase, ⁇ -L-iduronidase, iduronate sulfatase, ⁇ -mannosidase or sialidase.
  • the lysosomal enzyme can be a human glucocerebrosidase or human ⁇ -L-iduronidase.
  • the present invention provides for a plant transformation or transfection vector comprising any of the recombinant expression construct recited above.
  • the present invention provides for a plant which is transformed or transfected with any of the recombinant expression construct recited above.
  • the present invention provides for a plant cell, tissue or organ which is transformed or transfected with any of the recombinant expression construct recited above.
  • the present invention provides for a plasmid comprising any of the recombinant expression construct recited above.
  • the present invention provides for a transgenic plant or plant cell capable of producing a lysosomal enzyme which is enzymatically active, which transgenic plant or plant cell is transformed or transfected with a recombinant expression construct comprising a nucleotide sequence encoding a lysosomal enzyme and a promoter that regulates expression of the nucleotide sequence in the transgenic plant or plant cell.
  • the promoter is an inducible promoter.
  • the inducible promoter is induced by mechanical gene activation.
  • the lysosomal enzyme which is a modified lysosomal enzyme which is enzymatically active and which comprises: (a) an enzymatically-active fragment of a human or animal lysosomal enzyme; (b) the human or animal lysosomal enzyme or (a) having one or more amino acid residues added to the amino or carboxyl terminus of the human or animal lysosomal enzyme or (a); or (c) the human or animal lysosomal enzyme or (a) having one or more naturally-occurring amino acid additions, deletions or substitutions.
  • the modified lysosomal enzyme comprises a signal peptide or detectable marker peptide at the amino or carboxyl terminal of the modified lysosomal enzyme.
  • the modified lysosomal enzyme comprises: (a) an enzymatically-active fragment of an ⁇ -N-acetylgalactosaminidase, acid lipase, ⁇ -galactosidase, glucocerebrosidase, ⁇ -L-iduronidase, iduronate sulfatase, ⁇ -mannosidase or sialidase; (b) the ⁇ -N-acetylgalactosaminidase, acid lipase, ⁇ -galactosidase, glucocerebrosidase, ⁇ -L-iduronidase, iduronate sulfatase, ⁇ -mannosidase, sialidase or (a) having one or more amino acid residues added to the amino or carboxyl terminus of the ⁇ -N-acetylgalactosaminidase, acid lipase, ⁇ -galactosaminidas
  • the modified lysosomal enzyme can comprise: (a) an enzymatically-active fragment of a human glucocerebrosidase or human ⁇ -L-iduronidase enzyme; (b) the human glucocerebrosidase, human ⁇ -L-iduronidase or (a) having one or more amino acid residues added to the amino or carboxyl terminus of the human glucocerebrosidase, human ⁇ -L-iduronidase or (a); or (c) the human glucocerebrosidase, human a-L-iduronidase or (a) having one or more naturally-occurring amino acid additions, deletions or substitutions.
  • the modified lysosomal enzyme is a fusion protein comprising: (I) (a) the enzymatically-active fragment of the human or animal lysosomal enzyme, (b) the human or animal lysosomal enzyme, or (c) the human or animal lysosomal enzyme or (a) having one or more naturally-occurring amino acid additions, deletions or substitutions, and (II) a cleavable linker fused to the amino or carboxyl terminus of (I).
  • the transgenic plant or plant cell is a transgenic tobacco plant or tobacco cell.
  • the lysosomal enzyme is a human or animal lysosomal enzyme.
  • the lysosomal enzyme is an a-N-acetylgalactosaminidase, acid lipase, a-galactosidase, glucocerebrosidase, a-L-iduronidase, iduronate sulfatase, a-mannosidase or sialidase.
  • the lysosomal enzyme is a human glucocerebrosidase or human a-L-iduronidase.
  • the present invention provides for a leaf, stem, root, flower or seed of any of the transgenic plant recited above.
  • the present invention provides for a seed of plant line Nicotiana sp., which seed has the ATCC Accession No. PTA-2258, deposited Jul. 25, 2000.
  • the present invention provides for a plant grown from the seed recited above.
  • the present invention provides for a lysosomal enzyme which is enzymatically active and is produced according to a process comprising: recovering the lysosomal enzyme from (i) a transgenic plant cell or (ii) a cell, tissue or organ of a transgenic plant which transgenic plant cell or plant is transformed or transfected with a recombinant expression construct comprising a nucleotide sequence encoding the lysosomal enzyme and a promoter that regulates expression of the nucleotide sequence so that the lysosomal enzyme is expressed by the transgenic plant cell or plant.
  • the promoter can be an inducible promoter.
  • the process is carried out with the transgenic plant and additionally can comprise a step of inducing the inducible promoter before or after the transgenic plant is harvested, which inducing step is carried out before recovering the lysosomal enzyme from the cell, tissue or organ of the transgenic plant.
  • the modified lysosomal enzyme which can be enzymatically active and can comprise: (a) an enzymatically-active fragment of a human or animal lysosomal enzyme; (b) the human or animal lysosomal enzyme or (a) having one or more amino acid residues added to the amino or carboxyl terminus of the human or animal lysosomal enzyme or (a); or (c) the human or animal lysosomal enzyme or (a) having one or more naturally-occurring amino acid, additions, deletions or substitutions.
  • the modified lysosomal enzyme can comprise a signal peptide or detectable marker peptide at the amino or carboxyl terminal of the modified lysosomal enzyme.
  • the modified lysosomal enzyme can comprise: (a) an enzymatically-active fragment of an ⁇ -N-acetylgalactosaminidase, acid lipase, ⁇ -galactosidase, glucocerebrosidase, ⁇ -L-iduronidase, iduronate sulfatase, ⁇ -mannosidase or sialidase; (b) the ⁇ -N-acetylgalactosaminidase, acid lipase, ⁇ -galactosidase, glucocerebrosidase, ⁇ -Liduronidase, iduronate sulfatase, ⁇ -mannosidase, sialidase or (a) having one or more amino acid residues added to the amino or carboxyl terminus of the ⁇ -N-acetylgalactosaminidase, acid lipase, ⁇ -galactos
  • the modified lysosomal enzyme comprises: (a) an enzymatically-active fragment of a human glucocerebrosidase or human ⁇ -L-iduronidase enzyme; (b) the human glucocerebrosidase, human ⁇ -L-iduronidase or (a) having one or more amino acid residues added to the amino or carboxyl terminus of the human glucocerebrosidase, human ⁇ -L-iduronidase or (a); or (c) the human glucocerebrosidase, human ⁇ -L-iduronidase or (a) having one or more naturally-occurring amino acid additions, deletions or substitutions.
  • the modified lysosomal enzyme can be a fusion protein comprising: (I) (a) the enzymatically-active fragment of the human or animal lysosomal enzyme, (b) the human or animal lysosomal enzyme, or (c) the human or animal lysosomal enzyme or (a) having one or more naturally-occurring amino acid additions, deletions or substitutions, and (II) a cleavable linker fused to the amino or carboxyl terminus of (I).
  • the transgenic plant can be a transgenic tobacco plant.
  • the lysosomal enzyme can be a human or animal lysosomal enzyme.
  • the lysosomal enzyme can be an ⁇ -N-acetylgalactosaminidase, acid lipase, ⁇ -galactosidase, glucocerebrosidase, ⁇ -L-iduronidase, iduronate sulfatase, ⁇ -mannosidase or sialidase.
  • the lysosomal enzyme can be a human glucocerebrosidase or human ⁇ -L-iduronidase.
  • the organ can be a leaf, stem, root, flower, fruit or seed.
  • Gal-A is one of many proteins that require glycan site occupancy at N-linked sites to achieve proper folding and stability. The ability to successfully target the enzyme in Fabry patients is also likely to be glycosylation-dependent. This requirement presently limits the expression possibilities to eukaryotic cell types. Recombinant proteins synthesized in baculovirus and yeast expression systems are often hyperglycosylated and highly heterogeneous complicating the preparation of therapeutically effective glycoforms from these sources. The rGal-A synthesized in plants is a relatively homogeneous glycoform as analyzed by its SDS-PAGE electrophoretic mobility and comigrates with rGal-A produced purified from placenta (FIG. 3).
  • Protein pharmaceuticals may vary over five orders of magnitude in unit value and be required in kg/year quantities.
  • the example of Gaucher disease emphasizes the need progress in production phase research. Many additional heritable metabolic disorders, particularly those caused by dysfunctional lysosomal enzymes, might be treated by supplementation with exogenously produced enzymes. Enzyme replacement using macrophage-targeted human glucocerebrosidase has been shown to be extraordinarily beneficial for Gaucher patients. However, the cost of this treatment is very great. If the significant advances in clinical research are to be applied on a practical scale, new production technologies will be required to deliver bioproducts such as these to those in need at an affordable cost (43). No savings in Gaucher treatment costs were realized upon introduction of the recombinant CHO-cell product CerezymeTM to replace the placental-derived CeredaseTM. A significant reduction in cost requires fundamental changes in both the source of enzyme and process of purification.
  • vacuolar proteins do not require N-linked oligosaccharides for correct sorting into vacuoles (35,37,38).
  • Some vacuolar proteins (osmotin, thaumatin, chitinase-I, glucanase-I and a barley lectin), contain sorting information in a CTPP of 7 to 22 AA in length. For several of these proteins secreted isoforms are synthesized without a CTPP domain. In other cases, experimental deletion of the CTPP results in secretion of the recombinant protein to the IF (45-48). Sorting of Gal-A to the lysosome is likely to occur by the well-characterized mannose-6-phosphate receptor pathway in mammalian cells.
  • Galactosidase activity was stable in crude IF extracts and was bound to the hydrophobic interaction resin octyl sepharose, and eluted in a descending ammonium sulfate gradient.
  • the lectin resin concanavalin-A sepharose was also effective, indicating the presence of at least one high mannose chain.
  • the enzyme did not bind to a commercially available melibiose column (Sigma).
  • the facility has other major unit processes available for the recovery and purification of plant fractions.
  • the solvent extraction facility also has a biphasic solvent extractor and high efficiency distillation column. Extensive tankage was available both indoors and outdoors. Pumps, filters and other process equipment are available at the facility, allowing a large margin of flexibility while developing new processes.
  • the Bioprocess Facility has excellent supporting infrastructure.
  • the 900 square foot laboratory was equipped with all the basic tools for biochemical and protein analyses including: electrophoresis, gel filtration, HPLC, spectrophotometry, basic chromatography, chemical analysis, and sample preparation and preservation.
  • the full scale pilot plant has approximately 15,000 square feet of additional floor space for expansion including a high bay tower.
  • External solvent tanks are placed in diked enclosures.
  • Two rapid recovery, high pressure (up to 600 psi) steam generators and a large twin screw, oilless compressor are on site.
  • a complete shop and maintenance facility was present along with walk-in cold room and walk-in freezer. Additional equipment includes a ceramic microfiltration system, a spray dryer and an array of tanks, pumps, filters, heat exchangers, and agitators.
  • Process equipment was fabricated and modified by a group of skilled vendors and craftsmen capable of fabricating specialized equipment designed by the company, and has excellent field experience working in large scale operations.
  • Vacuum infiltration can be accomplished in the field or at the processing facility. Development experiments determine the necessity to infiltrate the material in the field.
  • a vacuum tank was used as the receiver for the plant tissue after harvest by the tobacco cutter. The tissue was conveyed into a trailer-mounted tank capable of full vacuum and slurried into an infiltration buffer.
  • the Owensboro facility has a trailer capable of carrying approximately 18,000 lb. This will translated into approximately 1,000 gallons per trip to the field.
  • the trailer was fitted with a 2,000 gallon tank capable of full volume and evacuated by a gasoline driven vacuum pump. In harvests from 1991-1994, it was the goal of the team to have harvested biomass at the processing facility in less than 1 hour after cutting.
  • the biomass can be brought from the field in the conventional wagon and infiltrated at the processing facility.
  • Several large, full vacuum tanks can be employed at the facility to increase the total throughput of the plant.
  • Two large-scale vacuum pump systems in the plant that are currently associated with the Alar rotary vacuum filters can be used for the vacuum infiltration process step.
  • Basket Centrifugation The full-scale basket-type centrifuge was a discontinuous batch-type system. Leaf tissue can be slurried in, dewatered as a batch, then a scraper system discharges the solids to a bottom dump. Large leaves and pieces of tissue can be handled in this manner.
  • the potential of placing a vacuum system on the discharge side of the centrifuge was also be investigated.
  • the centrifuge was a hydraulically driven conventional basket centrifuge with a bottom discharge and bowl dimension of 48 inches in diameter and a depth of 30 inches. Optimum loadings of the centrifuge in full-scale was determined the throughput and cycle times of this process step.
  • Vacuum extraction can be accomplished in large-scale by a web or belt-type vacuum filter system common in the food ingredient business.
  • the “in-plant” vacuum systems could also be adapted to operate this type of filter.
  • the plant tissue can be placed on this type of filter before or after the centrifugation step.
  • the initial UF separation was accomplished by an Alfa-Laval custom UF system consisting of six modular housings each containing either three 12 inch spiral wound membranes (Amicon type) or one standard 38 inch module. This yields a UF system with between 740 and 1140 square feet of membrane area of typical spiral wound configuration.
  • This system was housed in Clean Room # 1. This room is 14 ⁇ 18 ft, and is under positive pressure, HEPA-filtered air.
  • a second UF system was available in Clean Room #1. This smaller system, built by Separations Equipment Technology (SETEC), has the capacity for 320 square feet of spiral wound membrane. This system was employed for the second separation and diafiltration. It was designed for automatic diafiltration. Clean Room # 2 is equipped with a Pharmacia Streamline fluid bed gel filtration system equipped with UV and refractive index monitoring equipment. This unit was available for chromatography steps.
  • the vectors of the invention are based on chimeras between the 6.4 kb single-stranded RNA genome of tobacco mosaic virus (TMV) and other members of the tobamovirus group. Most of the TMV genome encodes overlapping reading frames required for replication and transcription (FIG. 1A). These are located at the 5′ end of the virus and translated from genomic RNA yielding proteins of 126 and 183 kDa. Expression of the internal genes was controlled by different promoters on the minus-sense RNA that direct synthesis of 3′-coterminal subgenomic mRNAs produced during replication.
  • TMV tobacco mosaic virus
  • TMV-based transient vectors offer significant advantages over integration of genes into plant chromosomes.
  • the vector invades virtually every cell of the plant during a period of 2 weeks post-inoculation.
  • the recombinant protein accumulates to several percent of the total protein during this brief period of time.
  • Many of these selections were culled because of poor expression due to position effects or gene silencing phenomena. In many more lines, the levels of product accumulation was too low for development of a viable commercial process.
  • rGCB human lysosomal enzyme
  • Leaf tissue was infiltrated with a suitable extraction buffer while submerged in a large vacuum chamber, allowing the solution to reach the leaf intercellular fluid containing rGCB.
  • the IF fraction was recovered by centrifugation in a custom collection chamber and “basket” centrifuge rotor compatible with a conventional Beckman J2-2 1 spindle.
  • rGCB was trapped from the dilute IF solution by expanded bed adsorption chromatography using a hydrophobic resin and eluted with polyethylene glycol.
  • a second ion exchange chromatography step was implemented for an overall yield of 1.7 mg/kg at 41% purity to this stage.
  • Transgenic Tobacco Leaves Express Moderate Levels of rGCB We combined a dual promoter from Cauliflower Mosaic Virus (35S), a translational enhancer from Tobacco Etch Virus and a polyadenylation region from the nopaline synthetase gene of Agrobacterium tumefaciens with the native human GCB cDNA to create plasmid pBSG638 (33; FIG. 14). These expression elements are widely used to provide the highest possible constitutive expression of nuclear encoded genes. Depending on the nature of individual proteins, these vectors can be used to accumulate moderate levels of recombinant proteins in most tissues of many plant species.
  • the lower % agar makes it easier to wash the agar off the roots when transferring to soil.
  • Plant rGCB is Similar to Macrophage-Targeted Glucocerebrosidase. We found reaction conditions to preferentially inhibit rGCB enzyme activity in the presence of plant glucosidases using the suicide substrate conduritol B-epoxide (CBE). Total glucosidase activity, and rGCB activity were measured by hydrolysis of the fluorescent substrate 4-methylumbelliferylglucopyranoside (4-MUG) with and without CBE. Total protein was determined by the method of Bradford. Detergents are necessary to solubilize and stabilize activity of this membrane-associated enzyme.
  • CBE conduritol B-epoxide
  • dialyzable bile salt, sodium taurocholate and the lower CMC detergent Tween-80 were compared at a range of concentrations (0.1-1% and 0.001-1%, respectively). Tween-80 at 0.15% and taurocholate at 0.5% gave the best yield and purity.
  • GCR native glucocerebrosidase
  • Two primary translation products are derived from two in-phase start codons. These precursors, a 2:1 mixture of 60 kDa and 57 kDa proteins, are proteolytically processed to 55 kDa as they pass into the lumen of the ER. High mannose and complex glycans are subsequently added in the ER and Golgi compartments to yield 62 and 66 kDa glycoforms. Finally, exoglycosidases generate a mature 59 kDa lysosomal enzyme.
  • rGCB As analyzed by SDS/PAGE, rGCB has an apparent molecular weight of 59 kDa, and comigrates with the mannose-terminal therapeutic glycoform.
  • PNGase F, Endo H, ⁇ 1-3 filcosidase glycosidases
  • the enzyme has an apparent molecular weight increase of 4 kDa over the proteolytically processed and unglycosylated form (55 kDa) and must be glycosylated for activity. Additional digestions are in progress with a more extensive set of endo- and exoglycosidases and known plant glycoprotein controls.
  • N-Glycosidase A is reported to hydrolyze all types of N-glycan chains from glycopeptides and glycoproteins.
  • the signal peptide of rGCB is processed at the correct site.
  • a very small quantity of protein was prepared for sequence analysis by purification through Phenyl-Sepharose, ConA-Sepharose and RP-HPLC to produce a single band on SDS-PAGE comigrating with authentic glucocerebrosidase.
  • the sequence obtained was consistent with the known sequence of processed GCR (Table. 3). In this particular analysis, the first two positions were not resolved because some degradation occurred during sample preparation. Correct proteolytic cleavage of a signal peptide is also confirmed for a mouse antibody light chain molecule expressed in tobacco leaves (35).
  • Plant rGCB Accumulates in the Leaf Intercellular Fluid.
  • Leaves were removed from the plant at the petiole and slit down the midrib into two equal halves.
  • To obtain a total cellular homogenate one group of half-leaves was ground in the presence of 4 volumes of detergent extraction buffer (100 mM potassium phosphate pH 6, 5 mM EDTA, 10 mM ⁇ -mercaptoethanol and 0.5% w/v sodium taurocholate) with a mortar and pestle.
  • detergent extraction buffer 100 mM potassium phosphate pH 6, 5 mM EDTA, 10 mM ⁇ -mercaptoethanol and 0.5% w/v sodium taurocholate
  • the undisrupted half-leaves were rolled gently in Parafilm, placed in disposable tubes and the IF collected by low-speed centrifugation.
  • the IF fraction is quite clear and non pigmented and can be applied directly to Phenyl Sepharose hydrophobic resin.
  • T0 individuals described in Table 4 are by definition hemizygous. They contain various loci generated from independent insertion events, having no corresponding insert on the homologous chromosome.
  • the thirteen T0 individuals from Group A were self-pollinated and assayed for levels of enzyme expression in the T1 generation in order to analyze the effects of gene dosage (homozygotes versus hemizygotes) and to identify candidate T1 families for future seed increase. Kanamycin-resistant transgenic plants were randomly selected from segregating families and analyzed for rGCB expression.
  • the number of probable loci was estimated by chi-square analysis of the linked kanamycin-resistant phenotype at >95% confidence level.
  • silencing of genes in plants is a recently described phenomenon. Work has been done detailing a cellular surveillance mechanism that has apparently evolved to specifically degrade excess RNA (36). In one case, specific RNA cleavages near the 3′-end of the transcript initiate the removal of the transcript. Our description of the silencing of rGCB above 600 U/mg is the first association of silencing with a truncated protein, and may well be caused by a specific mRNA (and not protein) cleavage event. Gene silencing may determine an upper limit of expression attainable using constitutive transgene expression.
  • pBSG641 This plasmid contains the rGCB gene substituted into the coat protein region. The remaining portion of the entire genome was then placed under control of the 35S promoter. The promoter was designed to initiate RNA synthesis such that the correct 5′-end of TMV would be synthesized. A custom-designed, self-cleaving ribozyme sequence positioned at the end of the genome yields a native 3′-end upon cleavage. The vector was designed for synthesis of infectious transcripts in vivo from a chromosomally integrated locus and production of rGCB through viral amplification of subgenomic mRNA in the cytoplasm.
  • RNA co-suppression is the subject of issued U.S. Pat. No. 5,922,602 issued Jul. 13, 1999, the disclosure of which is incorporated herein by reference.
  • the rGCB enzyme itself, or a secondary metabolite resulting from enzymatic activity, or even rGCB RNA may induce the HR.
  • the placental homogenate procedure is adapted from Furbish et al., (10) starting with a 14,000 ⁇ g sedimented material. In a typical preparation 15-30 kg of fresh placentas were processed. The tobacco homogenate is based on the average of 2 typical 1 kg extractions of the leaf biomass.
  • the IF data is from an average of 5 small scale extraction experiments (2-200 grams fresh weight), and a single chromatography run of an IF concentrate. For comparative purposes all yields are normalized to 1 kg.
  • GenBank accession No. for glucocerebrosidase is M11080.
  • rGCB is concentrated in the leaf lamina and in the lab scale procedure the midrib was removed.
  • CBE inhibits human GCB.
  • the fluorescent value used to calculate activity is based on the difference in values with and without inhibitor present.
  • the fluorescent value with CBE plant glucosidase
  • the assay is carried out using 5 ⁇ l of sample with 45 ⁇ l assay buffer ⁇ CBE at 37° C. This means that 2 tubes are needed per sample. This procedure is applicable to the Glucocerebrosidase assay procedure requiring a methylumbelliferone standard curve.
  • Test Tubes 13 ⁇ 100 mm glass (VWR or equivalent)
  • the fluorometer should be warmed up for at least 20 minutes prior to reading samples.
  • the power switch should be left on at all times. If the power switch was turned off it may take longer (up to 1 hour) for the instrument to stabilize.
  • Routine dilutions of samples should be carried out on ice using the GCB Assay Buffer described above to maintain enzyme activity. Generally a 1:5 or 1:10 dilution of the sample is sufficient. Dilutions should be carried out in a microfuge tube. ( Example: 1:10 dilution: 5 ⁇ l of sample in 45 ⁇ l of assay buffer, mix well and pulse sample in microfuge to bring all of the sample to the bottom of the tube). You should only need 5-10 ⁇ l of your sample for the dilutions.
  • Glucocerebrosidase (GCB), either derived from human placental tissue or a recombinant form from Chinese hamster ovary cells (CHO), is presently used in an effective but costly treatment of the heritable metabolic storage disorder known as Gaucher disease.
  • a dual promoter from Cauliflower Mosaic Virus (35S), a translational enhancer from Tobacco Etch Virus and a polyadenylation region from the nopaline synthetase gene of Agrobacterium tumefaciens with the native human GCB cDNA to create plasmid pBSG638.
  • These expression elements are widely used to provide the highest possible constitutive expression of nuclear encoded genes in plants.
  • the CaMV promoter is further inducible by stress or wound treatment.
  • one group of half-leaves was ground in the presence of 4 volumes of detergent extraction buffer (100 mM potassium phosphate p(I 6, 5 mM EDTA, 10 mM, B-mercaptoethanol and 0.5% w/v sodium taurocholate) with a mortar and pestle after freezing the tissue in liquid nitrogen.
  • detergent extraction buffer 100 mM potassium phosphate p(I 6, 5 mM EDTA, 10 mM, B-mercaptoethanol and 0.5% w/v sodium taurocholate
  • IF intercellular fluid
  • the same enzyme extraction buffer was infiltrated into the opposing group of half-leaves by submerging the tissue and applying moderate vacuum pressure (500 mm Hg). After draining off excess buffer, the undisrupted half-leaves were rolled gently in Parafilm, placed in disposable tubes and the intercellular fluid (IF) was collected by low-speed centrifugation (1,000 g).
  • GCB expression in IF extracts was quantified using a commercially available enzyme assay reagents and protocol. Total protein was determined by the method described by Bradford (Bradford, M. Anal. Biochem 72:248, 1976).
  • GCB assay is based on MUG hydrolysis in the presence of CBE.
  • the IF method results in a recovery of 22% of the total GCB activity of the leaf at a 18-fold enrichment relative to an extract obtained by homogenization (H).
  • the GCB production results may be improved by optimizing the time post-inoculation with the viral vector and minimizing the contaminating viral coat protein from the intercellular fraction.
  • MD609 leaf tissue (1-2 kilograms) of transgenic tobacco expressing the lysosomal enzyme glucocerebrosidase was harvested, the mid vein removed and the tissue weighed. Tissue was submerged with 2-4 volumes of buffer (0.1 M KPO 4 buffer, pH 6.0, 5 mM EDTA, 0.5% taurocholic acid, 10 mM ⁇ -mercaptoethanol) in an infiltration vessel that accommodates several kilograms of leaf tissue at one time. A perforated metal plate was placed on top of tissue to weigh down the tissue. A vacuum of 25-27 in. Hg was applied for 1-2 minutes ⁇ 3. The vacuum was released between subsequent applications. Tissue was rotated and the vacuum reapplied to achieve complete infiltration.
  • buffer 0.1 M KPO 4 buffer, pH 6.0, 5 mM EDTA, 0.5% taurocholic acid, 10 mM ⁇ -mercaptoethanol
  • the buffer may be drained from the infiltration vessel (spent buffer) and pooled with the 1st and 2nd IF fractions.
  • IF-1, IF-2 and Spent Buffer constitutes the IF pool.
  • the volume of intercellular fluid collected from the infiltrated leaf tissue was between 50-100% of the leaf tissue by weight depending on the number of infiltrations carried out.
  • Recombinant GCB was purified by loading the dilute intercellular (feed stream) directly on a Pharmacia Streamline 25 column containing Phenyl Streamline resin. Expanded bed chromatography enabled us to capture, clarify and concentrate our protein in one step without the need for centrifugation and/or microfiltration steps. The column was equilibrated and washed until UV-signal on recorder returned to baseline with 25 mM citrate, 20% ethylene glycol, pH 5.0 and then eluted with 25 mM citrate, 70% ethylene glycol.
  • the eluted material was further purified on a cation exchange resin, SP Big Beads (Pharmacia), equilibrated in 25 mM citrate, 75 mM NaCl, pH 5.0.
  • GCB was eluted with either a step gradient of 25 mM citrate, 0.5 M NaCl, 10% ethylene glycol, pH 5.0 or a linear gradient of 75 mM-0.4 M NaCl in 25 mM citrate, pH 5.0. All chromatography steps were carried out at room temperature.
  • glucocerebrosidase activity was achieved using the suicide substrate, conduritol ⁇ -epoxide (CBE), inhibition of recombinant glucocerebrosidase (rGCB) activity in the presence of plant glucosidases.
  • Enzyme activity was measured at 37° C. in a reaction mixture containing 5 mM methylumbelliferyl ⁇ -D glucoside, 0.1 M Potassium Phosphate, 0.15% Triton-X100, 0.125% sodium taurocholate, 0.1% bovine serum albumin, pH 5.9 with and without CBE.
  • Total glucosidase activity and rGCB activity were measured by hydrolysis of the fluorescent substrate 4-methylumbelliferyl glucopyranoside.
  • One unit of activity is defined as the amount of enzyme required to catalyze the hydrolysis of 1 nmol of substrate per hour.
  • Total protein was determined using the Bio-Rad Protein Assay based on the method of Bradford (Bradford, M. Anal. Biochem. 72:248; 1976).
  • IF-1, IF-2 and Spent Buffer constitutes the IF pool.
  • the IF pool was filtered through Miracloth and then concentrated 6 fold by passing the IF pool through a 1 sq. ft. spiral membrane (30K molecular weight cutoff) using an Amicon RA 2000 concentrator equipped with an LP-1 pump.
  • glucocerebrosidase activity was achieved using the suicide substrate, conduritol ⁇ -epoxide (CBE), inhibition of recombinant glucocerebrosidase (rGCB) activity in the presence of plant glucosidases.
  • Enzyme activity was measured at 37° C. in a reaction mixture containing 5 mM methylumbelliferyl ⁇ -D glucoside, 0.1 M Potassium Phosphate, 0.15% Triton-X100, 0.125% sodium taurocholate, 0.1% bovine serum albumin, pH 5.9 with and without CBE.
  • Total glucosidase activity and rGCB activity were measured by hydrolysis of the fluorescent substrate 4-methylumbelliferyl glucopyranoside.
  • One unit of activity is defined as the amount of enzyme required to catalyze the hydrolysis of 1 nmol of substrate per hour.
  • Total protein was determined using the Bio-Rad Protein Assay based on the method of Bradford (Bradford, M. Anal. Biochem. 72:248; 1976).
  • the intercellular fluid (IF) was recovered from the vacuum infiltrated leaves by centrifugation (1,800 ⁇ g, 30 minutes) using a Heine basket centrifuge (bowl dimensions, 28.0 inches diameter ⁇ 16.5 inches). Collected IF was filtered through a 50 uM cartridge filter and then stored at 4° C., until the entire 100 kilograms of tissue was infiltrated. This process was repeated with the next set of four 5 kg bags (5 ⁇ 20 Kg cycles total) until all the tissue was infiltrated. Additional buffer was added during each infiltration cycle to completely immerse the tissue. Alternatively, the leaf tissue can be re-infiltrated by placing the leaves back in the infiltration vessel in the same buffer used above and the process repeated (IF-2).
  • the buffer may be drained from the infiltration vessel (spent buffer) and may be pooled with the 1st and 2nd IF fractions.
  • IF-1, IF-2 and Spent Buffer constitutes the IF pool.
  • the volume of intercellular fluid collected from the infiltrated leaf tissue was between 42-170% of the leaf tissue by weight depending on the number of infiltrations carried out.
  • Recombinant GCB was purified by loading the dilute intercellular (feed stream) directly on a Pharmacia Streamline 200 column containing Phenyl Streamline resin. Expanded bed chromatography enabled us to capture, clarify and concentrate our protein in one step without the need for centrifugation and/or microfiltration steps.
  • the column was equilibrated and washed until UV-signal on recorder returned to baseline with 25 mM citrate, 20% ethylene glycol, pH 5.0 and then eluted with 25 mM citrate, 70% ethylene glycol.
  • the eluted material was sterile filtered by passing the eluted material through a 1 sq. ft. 0.8 um Sartoclean GF capsule followed by a 1 sq. ft.
  • Recombinant GCB was purified by loading the dilute intercellular (feed stream) directly on a Pharmacia Streamline 200 column containing Phenyl Streamline resin. The column was equilibrated and washed until UV-signal on recorder returned to baseline with 25 mM citrate, 20% ethylene glycol, pH 5.0 and then eluted with 25 mM citrate, 70% ethylene glycol. All chromatography steps were carried out at room temperature. Table 10 below contains data from the chops experiment.
  • a vacuum of 25-27 in. Hg was applied for 30 seconds and then quickly released.
  • the tissue was rotated and the vacuum reapplied to achieve complete infiltration which was confirmed by a distinct darkening in color of the underside of the leaf tissue.
  • Excess buffer on the tissue was drained.
  • the intercellular fluid was released from the tissue by centrifuging the tissue in a basket rotor at 3800 RPM (2100 ⁇ g) for 10-15 minutes.
  • the intercellular fluid was collected using an aspirator hooked up to a vacuum pump.
  • infected leaf tissue was harvested.
  • petioles and stems have been harvested along with the leaf tissue for infiltration. The mid vein was not removed from the tissue prior to infiltration.
  • Alpha galactosidase was purified by loading the dilute intercellular (fed stream) directly onto a Pharmacia Streamline 25 column containing Butyl Streamline resin. Expanded bed chromatography enabled us to capture, clarify and concentrate our protein in one step without the need for centrifugation and/or microfiltration steps. The column was equilibrated and washed until UV-signal on recorder returned to baseline with 25 mM Bis Tris Propane, pH 6.0 20% (NH 4 ) 2 S04 and then eluted with 25 mM Bis Tris Propane, pH 6.0.
  • the eluted material was further purified on Hydroxyapatite equilibrated with 1 mM NaPO 4 Buffer, 5% glycerol, pH 6.0 and eluted with either a 1-250 mM NaPO 4 buffer, 5% glycerol, pH 6.0 linear gradient or a step gradient. All chromatography steps were carried out at room temperature.
  • Alpha galactosidase activity was measured by hydrolysis of the fluorescent substrate 4-methylumbelliferyl a-D galactopyranoside. Enzyme activity was measured at 37° C. in a reaction mixture containing 5 mM methylumbelliferyl a-D galactopyranoside, 0.1 M Potassium Phosphate, 0.15% Triton-X100, 0.125% sodium taurocholate, 0.1% bovine serum albumin, pH 5.9. Total protein was determined using the Bio-Rad Protein Assay based on the method of Bradford (Bradford, M. Anal. Biochem. 72: 248; 1976).
  • Transgenic tobacco (MD609) expressing the lysosomal enzyme glucocerebrosidase was mechanically inoculated with a tobacco mosaic virus derivative containing a coat protein loop fusion, TMV291, (Turpen, et.al., 1995, Bio/Technology 13: 23-57).
  • TMV291 coat protein loop fusion
  • the metal basket containing the leaf material was placed in a 200 L Mueller vacuum tank containing ⁇ 100 liters of buffered solution (0.1 KPO 4 buffer, pH 6.0, 5 mM EDTA, 0.5% taurocholic acid, 10 mM ⁇ -mercaptoethanol).
  • buffered solution 0.1 KPO 4 buffer, pH 6.0, 5 mM EDTA, 0.5% taurocholic acid, 10 mM ⁇ -mercaptoethanol.
  • a 70 lb. stainless steel plate was placed over the leaves/bags to assure complete immersion.
  • a vacuum was pulled 27 in. Hg, held for 1 minute and then rapidly released. This vacuum infiltration was repeated for a total of two cycles. Multiple applications of the vacuum without isolating the intercellular fluid constitutes a single infiltration procedure.
  • An indication of complete infiltration is a distinct darkening in color of the underside of the leaf tissue. Following the vacuum infiltrations, the leaves and basket were removed from the vacuum tank.
  • the bags containing the vacuum infiltrated leaves were allowed to gravity drain surface buffer for ⁇ 10 minutes, prior to centrifugation.
  • the intercellular fluid (IF) was recovered from the vacuum infiltrated leaves by centrifugation (1,800 ⁇ g, 30 minutes) using a Heine basket centrifuge (bowl dimensions, 28.0 inches diameter ⁇ 16.5 inches). Collected IF was filtered through a 50 uM cartridge filter and then stored at 4° C., until the entire 100 kilograms of tissue was infiltrated. This process was repeated with the next set of four 5 kg bags (5 ⁇ 20 Kg cycles total) until all the tissue was infiltrated. Additional buffer was added during each infiltration cycle to completely immerse the tissue.
  • Recombinant GCB was purified by loading the dilute intercellular (feed stream) directly on a Pharmacia Streamline 200 column containing Phenyl Streamline resin. Expanded bed chromatography enabled us to capture, clarify and concentrate our protein in one step without the need for centrifugation and/or microfiltration steps.
  • the column was equilibrated and washed until UV-signal on recorder returned to baseline with 25 mM citrate, 20% ethylene glycol, pH 5.0 and then eluted with 25 mM citrate, 70% ethylene glycol.
  • the eluted material was sterile filtered by passing the eluted material through a 1 sq. ft. 0.8 um Sartoclean GF capsule followed by a 1 sq. ft.
  • the quantity of virus present in IF extracted leaf tissue was determined using homogenization and polyethylene glycol precipitation methods. In addition, the amount of virus present in the pooled, intercellular fluid was determined by direct polyethylene glycol precipitation. Final virus yields from precipitated samples was determined spectrophotometrically by absorbance at 260 nm. TABLE 8 Sample Virus Titer IF extracted leaf tissue 0.206 mg virus/g fresh weight Pooled IF 0.004 mg virus/g fresh weight, 0.010 mg virus/ml IF
  • Transcripts were prepared in vitro and inoculated onto the lower leaves of whole plants (Nicotiana benthamiana). 1-3 weeks after inoculation, leaves were weighed, rolled in a strip of Parafilm and placed in a disposable chromatography column and submerged in enzyme extraction buffer (0.1 M K/P04, 0.1 M NaCl, 5 mM EDTA, 10 mM ⁇ -ME and 0.5% sodium taurocholate, pH 6.0). In order to infiltrate the buffer into the tissue, a vacuum of 730-750 mmHg was twice applied. After draining the excess buffer, the intercellular fluid fraction was recovered by low-speed centrifugation ( ⁇ 1,500 ⁇ g, 15 min).
  • vacuolar sorting information is located in a carboxy-terminal propeptide (CTPP; 37,38).
  • CTPP carboxy-terminal propeptide
  • a cathepsin-like potential CTPP cleavage for this enzyme at or near two arginine residues, 26 and 28 AA from the termination codon (39,40).
  • the precise AA sequence at the carboxy terminus has, to our knowledge, never been reported. Because secretion in the plant leaf is through a default pathway we reasoned that deletion of specific sorting information from a postulated CTPP might yield more active enzyme in the IF.
  • the deletion vectors were designated as described in Table 10: TABLE 10 Vector Carboxy-Terminal Modifications Designation (Amino Acid Sequence) rGAL-A TSRLRSHINPTGTVLLQLENTM (SEQ ID NO: 23) QMSLKDLL rGAL-AR TSRLRSHINPTGTVLLQLENTM (SEQ ID NO: 24) QMSLKDLLSEKDEL rGAL-4 TSRLRSHINPTGTVLLQLENTM (SEQ ID NO: 25) QMSL rGAL-4R TSRLRSHINPTGTVLLQLENTM (SEQ ID NO: 26) QMSLSEKDEL rGAL-8 TSRLRSHINPTGTVLLQLENTM (SEQ ID NO: 27) rGAL-8R TSRLRSHINPTGTVLLQLENTM (SEQ ID NO: 28) SEKDEL rGAL-12 TSRLRSHINPTGTVLLQL (SEQ ID NO: 29) rGAL-12R
  • the ⁇ -galactosidase gene fragment present in vector rGAL-12R was placed into TMV vector SBS5.
  • the rice (x-amylase signal peptide present in rGAL-12R was replaced by the native human ⁇ -galactosidase signal peptide.
  • the resultant vector designated SBS5-rGAL-12R, see FIG. 13, exhibited genetic stability upon serial passage on N. benthamiana plants.
  • ⁇ -galactosidase was extracted from inoculated plants using interstitial fluid and homogenization methods. Fluids were analyzed for ⁇ -galactosidase yield, enzyme activity and cellular partitioning and targeting, see Table 11. In all cases, infectious transcripts were prepared in vitro and inoculated onto the lower leaves of actively growing Nicotiana benthamiana plants. Characteristic viral symptoms, vein clearing and leaf curling, were noted ⁇ 6-8 dpi (days post inoculation). Tissue samples were obtained from infected plants 1-3 weeks after inoculation.
  • Extracts from IF and homogenates from post-IF leaf tissue were analyzed for enzymatic activity by the hydrolysis of the fluorescent substrate 4-methyl umbeliferyl ⁇ -D-galactopyranoside (4-MUG).
  • 4-MUG 4-methyl umbeliferyl ⁇ -D-galactopyranoside
  • Known standards and established protocols (Suzuki, K. Enzymatic diagnosis of sphingolipidoses. Meth. Enzy. 138:727, 1987.) were used to obtain the number of enzymatic units (nmoles of 4-MUG hydrolyzed per hour at 37° C.) per gram fresh weight of tissue harvested.
  • the interstitial fluid (IF) was recovered from the vacuum infiltrated leaves by centrifugation (1,800 ⁇ G, 30 minutes) using a HeineS basket centrifuge (bowl dimensions, 28.0 inches diameter ⁇ 16.5 inches).
  • the IF was filtered through a 50 ⁇ m cartridge filter to remove plant debris prior to purification.
  • the eluent was filtered through a Sartorius glass fiber ⁇ 0.8 um cartridge filter and loaded directly onto 3 liters of Blue Sepharose in a Pharmacia BPG 200 column equilibrated with 25 mM Imidizole, pH 6.0.
  • the column was washed to UV baseline with 25 mM Imidizole, pH 6.0 and ⁇ gal was eluted with a step gradient of 25 mM Imidizole, 650 mM NaCl, pH 6.0.
  • the eluent was concentrated using a 10 kD MWCO, cellulose acetate, 3 ft 2 spiral membrane in an Amicon CH-2 concentrator and then sterile filtered.
  • Alpha gal activity was measured throughout the process with a fluorescent assay using the synthetic substrate, 4-methylumbelliferyl- ⁇ -D-galactopyranoside (MU- ⁇ gal).
  • Enzyme activity was measured at 37° C. in a reaction mixture containing 5 mM methylumbelliferyl ⁇ -D-galactopyranoside, 0.1 M Potassium Phosphate, 0.15% Triton-X100, 0.125% sodium taurocholate, and 0.1% bovine serum albumin, pH 5.9.
  • One unit of enzymatic activity hydrolyzes 1 nmol of MU- ⁇ -gal per hour at 37° C. Total protein was determined using the Bio-Rad Protein Assay based on the method of Bradford (Bradford, M. Anal.
  • N-terminal sequence analysis of ⁇ -galactosidase purified from plants inoculated with transcripts derived from the vector rGAL-12R, MLDNGLARTPT (see SEQ ID NO: 1), had a 100% sequence homology to 11 amino acids of human placental ⁇ -galactosidase with the addition of an N-terminal methionine.
  • N-terminal sequence of ⁇ -galactosidase, purified from plants inoculated with transcripts derived from the vector SBS5-rGAL-12R, LDNGLARTPT was as expected from native human enzyme.
  • C-Terminal sequence of the rGAL-12R and SBS5-rGAL-12R plant produced enzyme was obtained by Edman degradation using the commercial service of the Mayo Foundation. Three cycles were achieved before the signal was too low to read additional sequence.
  • the C-terminal amino acid was found to be heterogeneous, either L or E.
  • the presence of glutamic acid in the first cycle greatly reduced the signal because glutamic acid can form a cyclic structure during the activation step that disables cleavage from the chain and therefore blocks a portion of the sample to further sequencing. This reduced that ability of the software to interpret cycle 3 and beyond.
  • the presence of L, E and D in the first two cycles and the absence of other amino acids present in the analysis in an order resembling the ⁇ -galactosidase sequence strongly suggests that a population of the enzyme terminates with a DEL sequence as expected from the sequence of the DNA clone.
  • the molecular mass of several lots of plant derived ⁇ -galactosidase were determined by MALDI-TOF mass spectroscopy to be 48,963, 48,913, 49,100 daltons. These weights are consistent with the predicted mass of ⁇ -galactosidase, based upon amino acid sequence, allowing for broader peaks due to glycosylation.
  • the calculated molecular weight of SBS5-rGAL-12R derived ⁇ -galactosidase is 44,619. The difference in predicted and observed mass would equate to approximately 10.0% carbohydrate.
  • N—X-T/S N-glycosylation consensus sequences
  • human ⁇ gal A Matsuura, et. al. Glycobiology 8:329-339, 1998.
  • Plants have both high mannose and complex glycans that differ from mammalian complex glycans by the presence of an ⁇ 1,3 fucose on the proximal GlcNac and a ⁇ 1,2 xylose on the ⁇ -linked mannose of the core.
  • Four potential N-glycosylation sites have been identified for the plant derived ⁇ -galactosidase.
  • the predicted amino acid sequence has four possible glycosylation sites (Asn-Xaa-Ser/Thr) at Asn residues (108, 161, 184, 377).
  • the glycosylation site at amino acid 377 was not glycosylated, similar to CHO cell derived ⁇ -galactosidase glycosylation.
  • N-glycosylation sites are all located in ⁇ turns within hydrophilic regions of the enzyme. It was estimated the mature human ⁇ -galactosidase consists of about 370 amino acids and approx. 15% carbohydrate (Calhoun et al. PNAS 82: 7364-7368, 1985). Matsuura et al (Glycobiology 8:329-339,1998) reports that in CHO-cell produced ⁇ gal there are four N-glycosylation sites (139, 193, 215, 407) and 3 of the 4 sites are occupied (407 is not glycosylated).
  • ⁇ -galactosidase glycan structures were determined by MALDI-TOF and/or MALDI-MS in collaboration with the Universitaet fuer Bodenkultur, see Table 13.
  • MALDI 5 ⁇ g of plant derived ⁇ -galactosidase was digested with pepsin in a mass ratio of 1:40 in 5% formic acid. After evaporation the peptides were dissolved in ammonium acetate buffer, pH 5.0, boiled and subsequently digested with PNGase A overnight. Since the sample has a mass of 49.000 g/mol, there are 100 pmol of glycoprotein. After evaporation, the peptides were removed by cation exchange chromatography and the glycans are analyzed by MALDI (or pyridylaminated).
  • the molecular mass of the glycan was determined by MALDI-MS using a ThermoBio Analysis DYNAMO (linear MALDI-TOF MS with delayed extraction) instrument. A small portion of the sample was dried on the sample target and subsequently overlaid with “matrix” (gentisic acid). The samples contained complex type sugar chains with fucose, xylose and varying amounts of terminal GlcNAc. Small fractions were devoid of fucose and therefore amenable to hydrolysis by PNGase F.
  • This example demonstrates the ability to extract two different products from the same leaf tissue based upon extraction procedures that specifically target products localized in the apoplast and cytosol.

Abstract

The invention relates to α-galactosidase truncated at the carboxy terminus and the production of enzymatically active recombinant human and animal lysosomal enzymes involving construction and expression of recombinant expression constructs comprising coding sequences of human or animal lysosomal enzymes in a plant expression system. The plant expression system provides for post-translational modification and processing to produce a recombinant gene product exhibiting enzymatic activity. The invention is demonstrated by working examples in which transgenic tobacco plants express recombinant expression constructs comprising human glucocerebrosidase nucleotide sequences. The invention is also demonstrated by working examples in which transfected tobacco plants express recombinant viral expression constructs comprising human a galactosidase nucleotide sequences. The recombinant lysosomal enzymes produced in accordance with the invention may be used for a variety of purposes, including but not limited to enzyme replacement therapy for the therapeutic treatment of human and animal lysosomal storage diseases.

Description

    RELATED APPLICATIONS
  • The present application is a continuation of U.S. patent application Ser. No. 10/103,327, filed Mar. 20, 2002, and a continuation of U.S. patent application Ser. No. 09/993,059, filed Nov. 13, 2001, which is a continuation-in-part of U.S. patent application Ser. No. 09/626,127, filed Jul. 26, 2000; U.S. patent application Ser. No. 10/103,327, filed Mar. 20, 2002, is also a continuation of U.S. patent application Ser. No. 09/993,059, filed Nov. 13, 2001.[0001]
    • FIELD OF THE INVENTION
  • This invention is in the field of therapeutic peptides. Specifically this invention relates to the production of pharmaceutical peptides and proteins encoded on a recombinant plant virus or and produced by an infected plant or produced by a recombinant plant. The present invention relates especially to the production of human and animal lysosomal enzymes in plants comprising expressing the genetic coding sequence of a human or animal lysosomal enzyme in a plant expression system. The plant expression system provides for post-translational modification and processing to produce recombinant protein having enzymatic activity. The invention is demonstrated herein by working examples in which transgenic or transfected tobacco plants produce a modified human α galactosidase and a glucocerebrosidase, both of which are enzymatically active. The recombinant lysosomal enzymes produced in accordance with the invention may be used for a variety of purposes including but not limited to enzyme replacement therapy for the therapeutic treatment of lysosomal storage diseases, research for development of new approaches to medical treatment of lysosomal storage diseases, and industrial processes involving enzymatic substrate hydrolysis. [0002]
    • BACKGROUND OF THE INVENTION
  • Lysosomes, which are present in all animal cells, are acidic cytoplasmic organelles that contain an assortment of hydrolytic enzymes. These enzymes function in the degradation of internalized and endogenous macromolecular substrates. When there is a lysosomal enzyme deficiency, the deficient enzyme's undegraded substrates gradually accumulate within the lysosomes causing a progressive increase in the size and number of these organelles within the cell. This accumulation within the cell eventually leads to malfunction of the organ and to the gross pathology of a lysosomal storage disease, with the particular disease depending on the particular enzyme deficiency. More than thirty distinct, inherited lysosomal storage diseases have been characterized in humans. [0003]
  • Enzyme Replacement Therapy [0004]
  • One proven treatment for lysosomal storage diseases is enzyme replacement therapy in which an active form of the enzyme is administered directly to the patient. However, abundant, inexpensive and safe supplies of therapeutic lysosomal enzymes are not commercially available for the treatment of any of the lysosomal storage diseases. There are a large number of metabolic storage disorders known to affect man. As a group, these diseases are the most prevalent genetic abnormalities of humans, yet individually they are quite rare. One of the three major classes of these conditions, comprising the majority of patients, is the sphingolipidoses in which excessive quantities of undegraded fatty components of cell membranes accumulate because of inherited deficiencies of specific catabolic enzymes. Principal disorders in this category are Gaucher disease, Niemann-Pick disease, Fabry disease, and Tay-Sachs disease. All of these disorders are caused by harmful mutations in the genes that code for specific housekeeping enzymes within lysosomes. Thus, to be effective, enzyme replacement therapy requires that the requisite exogenous enzyme be taken up by the cells in which the materials are catabolized and that they be incorporated into lysosomes within these cells. Fabry disease is an ideal candidate for enzyme replacement therapy because the disease does not involve the central nervous system. The therapeutic enzyme does not need to be delivered across the blood-brain barrier (1, 2). [0005]
  • The effectiveness of enzyme replacement therapy has been dramatically documented in the treatment of patients with Gaucher disease. This condition is the most frequent of all metabolic storage disorders. It is estimated that there are 15,000 patients with this condition in the United States and about 80,000 worldwide. Soon after the enzymatic defect in Gaucher disease was established, consideration was given to the possibility of treating patients with purified α-glucocerebrosidase (3). Dr. Brady elected to use human placental tissue as the source of enzyme in order to minimize sensitizing patients to the exogenous protein. Initial studies with small amounts of glucocerebrosidase injected intravenously into patients with Gaucher disease revealed that the exogenous enzyme reduced the quantity of accumulated glucocerebroside in the liver and in the blood (4). A large-scale enzyme purification procedure was developed in order to obtain sufficient quantities for clinical efficacy trials (5). It was then learned that modifications of the terminal sugars on oligosaccharide chains of the enzyme were necessary in order to target intravenously administered enzyme to macrophages where most of the glucocerebroside is stored. Targeting to macrophages was accomplished by sequential enzymatic removal of monosaccharide residues from glucocerebrosidase resulting in mannose-terminal glucocerebrosidase (6). Administration of this glycoform of glucocerebrosidase to patients has brought about immense improvement in their condition (7-10). The modified enzyme (alglucerase) is now produced commercially by Genzyme Corporation in Cambridge, Mass., under the trade name Ceredase™. The beneficial effects of this treatment have been universally confirmed (11-13). Production of recombinant glucocerebrosidase (imiglucerase) is underway in Chinese hamster ovary (CHO) cells, and the product (Cerezyme™) is as effective as placental glucocerebrosidase (14). The experience with Gaucher treatment validates enzyme replacement therapy with a product that requires post-translational modifications. [0006]
  • Fabry disease is caused by deficiencies in the catalytic activity of the lysosomal enzyme a galactosidase A (Gal-A). Human Gal-A is a glycoprotein homodimer with a molecular weight of approximately 101 kDa containing 5-15% Asn-linked carbohydrate. The enzyme contains approximately equal portions of high mannose and complex type glycans. Upon isoelectric focusing, many forms of the enzyme are observed due to differences in sialylation depending on the source of the protein (tissue or plasma forms). The disease is inherited as an X-linked recessive trait. A number of specific mutations in the gene have been characterized, including partial rearrangements, splice-junction defects and point mutations. Most of these mutations are private and therefore, the gene appears to be highly mutable relative to genes encoding other housekeeping enzymes. Defects result in the accumulation of glycosphingolipid substrates, globotriaosylceramide and related glycolipids with terminal α-galactosidic linkages. Uncatabolized substrate accumulates in the plasma, vascular endothelium and various organs leading to an early demise from vascular disease of the heart, brain, and kidney, particularly in the classically affected hemizygous males. In addition to systemic disease, affected individuals often suffer from peripheral neuropathies and have characteristic angiokeratoma of the skin. Heterozygous female carriers may have a more attenuated range of disease phenotypes (1,2). [0007]
  • Exploratory trials of enzyme replacement therapy for Fabry disease have demonstrated the biochemical effectiveness of this approach (15-18). Repeated injections of purified splenic and plasma Gal-A reduced the level of plasma substrate and may have mobilized stored tissue substrate into circulation. No immunological complications were apparent in repeated infusions of enzyme into hemizygous males. Further investigations have not been attempted because of the great difficulty in obtaining sufficient quantities of enzyme for a meaningful replacement trial. The availability of large quantities of enzyme would enable optimization of glycoforms for therapeutic efficacy by improving cell targeting and prolonging the half-life in circulation and target organs. [0008]
  • α Galactosidase [0009]
  • In the early 1970's, several investigators demonstrated the existence of two .αa.-Galactosidase isozymes designated A and B, which hydrolyzed the α-galactosidic linkages in 4-MU-and/or rho-NP-α-D-galactopyranosides (62, 63, 64, 65, 66, 67, 68, 69) In tissues, about 80%-90% of total α-Galactosidase (α-Gal) activity was due to a thermolabile, myoinositol-inhibitable α-Gal A isozyme, while a relatively thermostable, α-Gal B, accounted for the remainder. The two “isozymes” were separable by electrophoresis, isoelectric focusing, and ion exchange chromatography. After neuraminidase treatment, the electrophoretic migrations and pI value of α-Gal A and B were similar (70), initially suggesting that the two enzymes were the differentially glycosylated products of the same gene. The finding that the purified glycoprotein enzymes had similar physical properties including subunit molecular weight (about 46 kDa), homodimeric structures, and amino acid compositions also indicated their structural relatedness (70. 71. 72. 73. 74. 75. 76. 77). However, the subsequent demonstration that polyclonal antibodies against α-Gal A or B did not cross-react with the other enzyme (78, 79) that only α-Gal A activity was deficient in hemizygotes with Fabry disease (80, 81, 82, 83, 84, 85, 86) and that the genes for α-Gal A and B mapped to different chromosomes (Desnick, et al., 1989, in The Metabolic Basis of Inherited Disease, Scriver, C. R., Beaudet, A. L. Sly, W. S. and Valle, D., eds, pp. 1751-1796, McGraw Hill, New York; deGroot, et al., 1978, Hum. Genet. 44:305-312), clearly demonstrated that these enzymes were genetically distinct. [0010]
  • α-GAL a and Fabry Disease [0011]
  • In Fabry disease, a lysosomal storage disease resulting from the deficient activity of α-Gal A, identification of the enzymatic defect in 1967 (Brady, et al., 1967, N. Eng. J. Med. 276:1163) led to the first in vitro (Dawson, et al., 1973, Pediat. Res. 7: 694-690m) and in vivo (Mapes, et al., 1970, Science 169:987) therapeutic trials of α-Gal A replacement in 1969 and 1970, respectively. These and subsequent trials (Mapes, et al., 1970, Science 169:987; Desnick, et al., 1979, Proc. Natl. Acad. Sci. USA 76: 5326; and, Brady, et al., 1973, N. Engl. J. Med. 289: 9) demonstrated the biochemical effectiveness of direct enzyme replacement for this disease. Repeated injections of purified splenic and plasma α-Gal A (100,000 U/injection) were administered to affected hemizygotes over a four month period (Desnick, et al., 1979, Proc. Natl. Acad. Sci. USA 76:5326). The results of these studies demonstrated that (a) the plasma clearance of the splenic form was 7 times faster than that of the plasma form (10 min vs 70 min); (b) compared to the splenic form of the enzyme, the plasma form effected a 25-fold greater depletion of plasma substrate over a markedly longer period (48 hours vs 1 hour); (c) there was no evidence of an immunologic response to six doses of either form, administered intravenously over a four month period to two affected hemizygotes; and (d) suggestive evidence was obtained indicating that stored tissue substrate was mobilized into the circulation following depletion by the plasma form, but not by the splenic form of the enzyme. Thus, the administered enzyme not only depleted the substrate from the circulation (a major site of accumulation), but also possibly mobilized the previously stored substrate from other depots into the circulation for subsequent clearance. These studies indicated the potential for eliminating, or significantly reducing, the pathological glycolipid storage by repeated enzyme replacement. However, the biochemical and clinical effectiveness of enzyme replacement in Fabry disease has not been commercially available due to the lack of sufficient human enzyme for adequate doses and longterm evaluation. [0012]
  • The α-Gal a Enzyme [0013]
  • The α-Gal A human enzyme has a molecular weight of approximately 101,000 Da. On SDS gel electrophoresis it migrates as a single band of approximately 49,000 Da indicating the enzyme is a homodimer (Bishop & Desnick, 1981, J. Biol. Chem. 256: 1307). α-Gal A is synthesized as a 50,500 Da precursor containing phosphorylated endoglycosidase H sensitive oligosaccharides. This precursor is processed to a mature form of about 46,000 Da within 3-7 days after its synthesis. The intermediates of this processing have not been defined (Lemansky, et al., 1987, J. Biol. Chem. 262:2062). As with many lysosomal enzymes, .α.-Gal A is targeted to the lysosome via the mannose-6-phosphate receptor. This is evidenced by the high secretion rate of this enzyme in mucolipidosis II cells and in fibroblasts treated with NH.sub.4 Cl. [0014]
  • The enzyme has been shown to contain 5-15% Asn linked carbohydrate (Ledonne, et al., 1983, Arch. Biochem. Biophys. 224:186). The tissue form of this enzyme was shown to have about 52% high mannose and 48% complex type oligosaccharides. The high mannose type coeluted, on Bio-gel chromatography, with Man.sub.8-9 GlcNAc while the complex type oligosaccharides were of two categories containing 14 and 19-39 glucose units. Upon isoelectric focusing many forms of this enzyme are observed depending on the sources of the purified enzyme (tissue vs plasma form). However, upon treatment with neuraminidase, a single band is observed (pI-5.1) indicating that this heterogeneity is due to different degrees of sialylation (Bishop & Desnick, 1981, J. Biol. Chem. 256:1307). Initial efforts to express the full-length cDNA encoding α-Gal A involved using various prokaryotic expression vectors (Hantzopoulos and Calhoun, 1987, Gene 57:159; Ioannou, 1990, Ph.D. Thesis, City University of New York). Although microbial expression was achieved, as evidenced by enzyme assays of intact [0015] E. coli cells and growth on melibiose as the carbon source, the human protein was expressed at low levels and could not be purified from the bacteria. These results indicate that the recombinant enzyme was unstable due to the lack of normal glycosylation and/or the presence of endogenous cytoplasmic or periplasmic proteases.
  • Gaucher Disease and Treatment [0016]
  • Gaucher disease is the most common lysosomal storage disease in humans, with the highest frequency encountered in the Ashkenazi Jewish population. About 5,000 to 10,000 people in the United States are afflicted with this disease (Grabowski, 1993, Adv. Hum. Genet. 21:377-441). Gaucher disease results from a deficiency in glucocerebrosidase (hGCB); glucosylceramidase; acid β-glucosidase; EC 3.2.1.45). This deficiency leads to an accumulation of the enzyme's substrate, glucocerebroside, in reticuloendothelial cells of the bone marrow, spleen and liver, resulting in significant skeletal complications such as bone marrow expansion and bone deterioration, and also hypersplenism, hepatomegaly, thrombocytopenia, anemia and lung complications (Grabowski, 1993, supra; Lee, 1982, Prog. Clin. Biol. Res. 95:177-217; Brady et al., 1965, Biochem. Biophys. Res. Comm. 18:221-225). hGCB replacement therapy has revolutionized the medical care and management of Gaucher disease, leading to significant improvement in the quality of life of many Gaucher patients (Pastores et al., 1993, Blood 82:408-416; Fallet et al., 1992, Pediatr. Res. 31:496-502). Studies have shown that regular, intravenous administration of specifically modified hGCB (Ceredase.™., Genzyme Corp.) can result in dramatic improvements and even reversals in the hepatic, splenic and hematologic manifestations of the disease (Pastores et al., 1993, supra; Fallet: et al., 1992, supra; Figueroa et al., 1992, N. Eng. J. Med 327:1632-1636; Barton et al., 1991, N. Eng. J. Med. 324:1464-1470; Beutler et al., 1991, Blood 78:1183-1189). Improvements in associated skeletal and lung complications are possible, but require larger doses of enzyme over longer periods of time. [0017]
  • Despite the benefits of hGCB replacement therapy, the source and high cost of the enzyme seriously restricts its availability. Until recently, the only commercial source of purified hGCB has been from pooled human placentae, where ten to twenty kilograms (kg) of placentae yield only 1 milligram (mg) of enzyme. From five hundred to two thousand kilograms of placenta (equivalent to 2,000-8,000 placentae) are required to treat each patient every two weeks. Current costs for hGCB replacement therapy range from $55 to $220/kg patient body weight every two weeks, or from $70,000 to $300,000/year for a 50 kg patient. Since the need for therapy essentially lasts for the duration of a patient's life, costs for the enzyme alone may exceed $15,000,000 during 30 to 70 years of therapy. [0018]
  • A second major problem associated with treating Gaucher patients with glucocerebrosidase isolated from human tissue (and perhaps even from other animal tissues) is the risk of exposing patients to infectious agents which may be present in the pooled placentae, e.g., human immuno-deficiency virus (HIV), hepatitis viruses, and others. [0019]
  • Accordingly, a new source of hGCB is needed to effectively reduce the cost of treatment and to eliminate the risk of exposing Gaucher patients to infectious agents. [0020]
  • Hurler Syndrome and Treatment [0021]
  • Hurler syndrome is the most common of the group of human lysosomal storage disorders known as the mucopolysaccharidosis (MPS) involving an inability to degrade dermatan sulfate and heparan sulfate. Hurler patients are deficient in the lysosomal enzyme, α-L-iduronidase (IDUA), and the resulting accumulation of glucosaminoglycans in the lysosomes of affected cells leads to a variety of clinical manifestations (Neufeld & Ash well, 1980, The Biochemistry of Glycoproteins and Proteoglycans, ed. W. J. Lennarz, Plenum Press, N.Y.; pp. 241-266) including developmental delay, enlargement of the liver and spleen, skeletal abnormalities, mental retardation, coarsened facial features, corneal clouding, and respiratory and cardiovascular involvement. Hurler/Scheie syndrome (MPS I H/S) and Scheie syndrome (MPS IS) represent less severe forms of the disorder but also involve deficiencies in IDUA. Molecular studies on the genes and cDNAs of MPS I patients has led to an emerging understanding of genotype and clinical phenotype (Scott et al., 1990, Am. J. Hum. Genet. 47:802-807). In addition, both a canine and feline form of MPS I have been characterized (Haskins et al., 1979, Pediat. Res. 13:1294-1297; Haskins and Kakkis, 1995, Am. J. Hum. Genet. 57:A39 Abstr. 194; Shull et al., 1994, Proc. Natl. Acad. Sci. USA, 91:12937-12941) providing an effective in vivo model for testing therapeutic approaches. [0022]
  • The efficacy of enzyme replacement in the canine model of Hurler syndrome using human IDUA generated in CHO cells was recently reported (Kakkis et al., 1995, Am. J. Hum. Genet. 57:A39 (Abstr.); Shull et al., 1994, supra). Weekly doses of approximately 1 mg administered over a period of 3 months resulted in normal levels of the enzyme in liver and spleen, lower but significant levels in kidney and Lungs and very low levels in brain, heart, cartilage and cornea (Shull et al., 1994, supra. Tissue examinations showed normalization of lysosomal storage in the liver, spleen and kidney, but no improvement in heart, brain and corneal tissues. One dog was maintained on treatment for 13 months and was clearly more active with improvement in skeletal deformities, joint stiffness, corneal clouding and weight gain (Kakkis et al., 1995, supra. A single higher-dose experiment was quite promising and showed detectable IDUA activity in the brain and cartilage in addition to tissues which previously showed activity at the lower does. Additional higher-dose experiments and trials involving longer administration are currently limited by availability of recombinant enzyme. These experiments underscore the potential of replacement therapy for Hurler patients and the severe constraints on both canine and human trials due to limitations in recombinant enzyme production using current technologies. [0023]
  • Lysosomal Enzymes: Biosynthesis and Targeting [0024]
  • Lysosomal enzymes are synthesized on membrane-bound polysomes in the rough endoplasmic reticulum. Each protein is synthesized as a larger precursor containing a hydrophobic amino terminal signal peptide. This peptide interacts with a signal recognition particle, an 11S ribonucleoprotein, and thereby initiates the vectoral transport of the nascent protein across the endoplasmic reticulum membrane into the lumen (Erickson, et al., 1981, J. Biol. Chem. 256:11224; Erickson, et al., 1983, Biochem. Biophys. Res. Commun. 115:275; Rosenfeld, et al., 1982, J. Cell Biol. 93:135). Lysosomal enzymes are cotranslationally glycosylated by the en bloc transfer of a large preformed oligosaccharide, glucose-3, mannose-9, N-acetylglucosamine-2, from a lipid-linked intermediate to the Asn residue of a consensus sequence Asn-X-Ser/Thr in the nascent polypeptide (Kornfeld, R. & Kornfeld, S., 1985, Annu. Rev. Biochem. 54:631). In the endoplasmic reticulum, the signal peptide is cleaved, and the processing of the Asn-linked oligosaccharide begins by the excision of three glucose residues and one mannose from the oligosaccharide chain. [0025]
  • The proteins move via vesicular transport, to the Golgi stack where they undergo a variety of posttranslational modifications, and are sorted for proper targeting to specific destinations: lysosomes, secretion, plasma membrane. During movement through the Golgi, the oligosaccharide chain on secretory and membrane glycoproteins is processed to the sialic acid-containing complex-type. While some of the oligosaccharide chains on lysosomal enzymes undergo similar processing, most undergo a different series of modifications. The most important modification is the acquisition of phosphomannosyl residues which serve as an essential component in the process of targeting these enzymes to the lysosome (Kaplan, et al., 1977, Proc. Natl. Acad. Sci. USA 74:2026). This recognition marker is generated by the sequential action of two Golgi enzymes. First, N-acetylglucosaminyl-phosphotransferase transfers N-acetylglucosamine-1-phosphate from the nucleotide sugar uridine diphosphate-N-acetylglucosamine to selected mannose residues on lysosomal enzymes to give rise to a phosphodiester intermediate (Reitman & Kornfeld, 1981, J. Biol. Chem. 256:4275; Waheed, et al., 1982, J. Biol. Chem. 257:12322). Then, N-acetylglucosamine-1-phosphodiester α-N-acetylglucosaminidase removes N-acetylglucosarnine residue to expose the recognition signal, mannose-6-phosphate (Varki & Kornfeld, 1981, J. Biol. Chem. 256: 9937; Waheed, et al., 1981, J. Biol. Chem. 256:5717). [0026]
  • Following the generation of the phosphomannosyl residues, the lysosomal enzymes bind to mannose-6-phosphate (M-6-P) receptors in the Golgi. In this way the lysosomal enzymes remain intracellular and segregate from the proteins which are destined for secretion. The ligand-receptor complex then exits the Golgi via a coated vesicle and is delivered to a prelysosomal staging area where dissociation of the ligand occurs by acidification of the compartment (Gonzalez-Noriega, et al., 1980, J. Cell Biol. 85: 839). The receptor recycles back to the Golgi while the lysosomal enzymes are packaged into vesicles to form primary lysosomes. Approximately, 5-20% of the lysosomal enzymes do not traffic to the lysosomes and are secreted presumably, by default. A portion of these secreted enzymes may be recaptured by the M-6-P receptor found on the cell surface and be internalized and delivered to the lysosomes (Willingham, et al., 1981, Proc. Natl. Acad. Sci. USA 78:6967). [0027]
  • Two mannose-6-phosphate receptors have been identified. A 215 kDa glycoprotein has been purified from a variety of tissues (Sahagian, et al., 1981, Proc. Natl. Acad. Sci. USA, 78:4289; Steiner & Rome, 1982, Arch. Biochem. Biophys. 214:681). The binding of this receptor is divalent cation independent. A second M-6-P receptor also has been isolated which differs from the 215 kDa receptor in that it has a requirement for divalent cations. Therefore, this receptor is called the cation-dependent (M-6-P.sup.CD) while the 215 kDa one is called cation-independent (M-6-P.sup.Cl). The M-6-P.sup.CD receptor appears to be an oligomer with three subunits with a subunit molecular weight of 46 kDa. [0028]
  • Biosynthesis of Lysosomal Enzymes [0029]
  • Although many lysosomal enzymes are soluble and are transported to lysosomes by M-6-P receptors (MPR), integral membrane and membrane-associated proteins such as human glucocerebrosidase (hGCB) are targeted and transported to lysosomes independent of the M-6-P/MPR system (Kornfeld & Mellman, 1989, Erickson et al., 1985). hGCB does not become soluble after translation, but instead becomes associated with the lysosomal membrane by means which have not been elucidated (von Figura & Hasilik, 1986, Annu. Rev. Biochem. 55:167-193; Kornfeld and Mellman, 1989, Annu. Rev. Cell Biol. 5:483-525). hGCB is synthesized as a single polypeptide (58 kDa) with a signal sequence (2 kDa) at the amino terminus. The signal sequence is co-translationally cleaved and the enzyme is glycosylated with a heterogeneous group of both complex and high-mannose oligosaccharides to form a precursor. The glycans are predominately involved in protein conformation. The “high mannose” precursor, which has a molecular weight of 63 KDa, is post-translationally processed in the Golgi to a 66 KDa intermediate, which is then further modified in the lysosome to the mature enzyme having a molecular weight of 59 KDa (Jonsson et al., 1987, Eur. J. Biochem. 164:171; Erickson et al., 1985, J. Biol. Chem., 260:14319). [0030]
  • The mature hGCB polypeptide is composed of 497 amino acids and contains five N-glycosylation amino acid consensus sequences (Asn-X-Ser/Thr). Four of these sites are normally glycosylated. Glycosylation of the first site is essential for the production of active protein. Both high-mannose and complex oligosaccharide chains have been identified (Berg-Fussman et al., 1993, J. Biol. Chem. 268:14861-14866). hGCB from placenta contains 7% carbohydrate, 20% of which is of the high-mannose type (Grace & Grabowski, 1990, Biochem. Biophys. Res. Comm. 168:771-777). Treatment of placental hGCB with neuraminidase (yielding an asialo enzyme) results in increased clearance and uptake rates by rat liver cells with a concomitant increase in hepatic enzymatic activity (Furbish et al., 1981, Biochim. Biophys. Acta 673:425-434). This glycan-modified placental hGCB is currently used as a therapeutic agent in the treatment of Gaucher's disease. Biochemical and site-directed mutagenesis studies have provided an initial map of regions and residues important to folding, activator interaction, and active site location (Grace et al., 1994, J. Biol. Chem. 269:2283-2291). [0031]
  • The complete complementary DNA (cDNA) sequence for hGCB has been published (Tsuji et al., 1986, J. Biol. Chem. 261:50-53; Sorge et al., 1985, Proc. Natl. Acad. Sci. USA 82:7289-7293), and [0032] E. coli containing the hGCB cDNA sequence cloned from fibroblast cells, as described (Sorge et al., 1985, supra), is available from the American Type Culture Collection (ATCC) (Accession No. 65696).
  • Recombinant methodologies have the potential to provide a safer and less expensive source of lysosomal enzymes for replacement therapy. However, production of active enzymes, e.g., hGCB, in a heterologous system requires correct targeting to the ER, and appropriate N-linked glycosylation at levels or efficiencies that avoid ER-based degradation or aggregation. Since mature lysosomal enzymes must be glycosylated to be active, bacterial systems cannot be used. For example, hGCB expressed in [0033] E. coli is enzymatically inactive (Grace & Grabowski, 1990, supra).
  • Active monomers of hGCB have been purified from insect cells (Sf9 cells) and Chinese hamster ovary (CHO) cells infected or transfected, respectively, with hGCB cDNA (Grace & Grabowski, 1990, supra; Grabowski et al., 1989, Enzyme 41:131-142). A method for producing recombinant hGCB in CHO cell cultures and in insect cell cultures was recently disclosed in U.S. Pat. No. 5,236,838. Recombinant hGCB produced in these heterologous systems had an apparent molecular weight ranging from 64 to 73 kDa and contained from 5 to 15% carbohydrate (Grace & Grabowski, 1990, supra; Grace et al., 1990, J. Biol. Chem. 265:6827-6835). These recombinant hGCBs had kinetic properties identical to the natural enzyme isolated from human placentae, as based on analyses using a series of substrate and transition state analogues, negatively-charged lipid activators, protein activators (saposin C), and mechanism-based covalent inhibitors (Grace et al., 1994, supra; Berg-Fussman et al., 1993, supra; Grace et al., 1990, J. Biol. Chem. 265:6827-6835; Grabowski et al., 1989, supra). However, both insect cells and CHO cells retained most of the enzyme rather than secreting it into the medium, significantly increasing the difficulty and cost of harvesting the pure enzyme (Grabowski et al., 1989, supra). Accordingly, a recombinant system is needed that can produce human or animal lysosomal enzymes in an active form at lower cost, and that will be appropriately targeted for ease of recovery. [0034]
  • Enormous Costs of Pharmaceutical Enzyme Production [0035]
  • While the clinical treatment of Gaucher patients provides a dramatically successful example of an effective therapy, the expense underscores an equally inadequate production technology. For example, the present cost for the first year of treatment for a severely affected 70 kg patient with Gaucher disease can reach $382,000. If the patient's clinical parameters are not restored to normal in that time, treatment at this level of expense will be prolonged before dose reduction can be initiated. Even with dose reduction, it is likely that the maintenance cost for such an individual will be in the range of $135,000 per year (at $3.70/IU). Many patients are unable to pay this large cost, and health carriers are extremely reluctant to underwrite this treatment for the life of these patients. Cerezyme™ is as expensive as Ceredase™ and at this time is available only in limited quantities. The number of patients with Gaucher disease in the US currently receiving therapy is estimated to be only 10-15% of the total. According an article in Nature Medicine, since the introduction of this therapy six years ago the cost of treating Gaucher patients worldwide will soon approach one billion dollars (19). Although the total number of patients worldwide who would benefit from therapy is not known with any certainty, it is safe to assume that at least 80% of the world Gaucher population remain untreated. To quote from the NIH Technology Assessment Conference Summary Statement, Feb. 27-Mar. 1, 1995. “As a prototype for all rare diseases, the plight of patients with Gaucher disease raises difficult financial and ethical issues, which we as a society must address (20).” Fabry disease is estimated to occur at a frequency of 1 in 40,000. Over 400 hemizygous male patients have been clinically described. It is imperative that fundamentally new methods of enzyme production be developed to reduce these costs so that all who suffer from these rare disorders can be treated. [0036]
  • Mammalian Lysosomes Versus Plant Vacuoles [0037]
  • Because plants are eukaryotes, plant expression systems have advantages over prokaryotic expression systems, particularly with respect to correct processing of eukaryotic gene products. However, unlike animal cells, plant cells do not possess lysosomes. Although the plant vacuole appears functionally analogous to the lysosome, plants do not contain MPRs (Chrispeels, 1991, Ann. Rev. Pl. Phys. Pl. Mol. Biol. 42:21-53; Chrispeels and Tague, 1991, Intl. Rev. Cytol. 125:1-45), and the mechanisms of vacuolar targeting can differ significantly from those of lysosomal targeting. For example, the predominant mechanism of vacuolar targeting in plants does not appear to be glycan-dependent, but appears to be based instead on C— or N-terminal peptide sequences (Gomez & Chrispeels, 1993, Plant Cell 5:1113-1124; Chrispeels & Raikhal, 1992, Cell 68:613-618; Holwerda et al., 1992, Plant Cell 4:307-318; Neuhaus et al., 1991, Proc. Natl. Acad. Sci. USA 88:10362-10366; Chrispeels, 1991, supra; Chrispeels & Tague, 1991, supra; Holwerda et al., 1990, Plant Cell 2:1091-1106; Voelker et al., 1989, Plant Cell 1:95-104). As a result, plants have not been viewed as appropriate expression systems for lysosomal enzymes which must be appropriately processed to produce an active product. [0038]
  • An object of this invention is to provide the existing patient population with enough active enzyme to develop a lower cost treatment. The enzymatic, structural, and glycan compositional analyses show rGal to be active. There are recent advances in glycoprotein modification and drug delivery that allow, as examples, the chemical conjugation of peptides to carbohydrate, the covalent addition of polyethylene glycol to enzymes and the liposomal encapsulation of protein. Many additional new concepts can be tested to increase the half-life of enzymes in circulation and optimize cellular and subcellular targeting. Ideally, these modifications will require a facile and rapid genetic system to produce large quantities of highly pure enzyme and an effective animal disease model for drug development. Our lab-scale process appears highly scalable and is capable of producing grams of enzyme per month in existing indoor greenhouse growth areas. [0039]
  • Using a viral transfection system and transgenic plants, we have expressed enzymes in plants that have potential as therapeutic agents for humans with the metabolic storage disorders known as Fabry disease and Gaucher disease. High specific activity recombinant enzymes were secreted by tobacco leaf cells via a default pathway of protein sorting into the apoplastic compartment, a network of extracellular space, cell wall matrix materials and intercellular fluid (IF). We further developed a novel bioprocessing method to purify these enzymes from the IF fraction. [0040]
  • Another object of this invention is to provide an optimized preproenzyme amino acid (AA) sequence for secretion of highly active lysosomal enzymes. Another object of this invention is to provide an optimized purification of lysosomal enzymes from either the IF fraction or from whole plant homogenates. Another object of this invention is to provide a molecular characterization of the enzymes purified by this process, including determination of enzyme specific activity. [0041]
    • SUMMARY OF THE INVENTION
  • The present invention provides for a polypeptide comprising (a) the complete, or a fragment of, the amino acid sequence of α-galactosidase with or without (b) an ER-retention signal, such as the amino acid sequence SEKDEL (SEQ ID NO:37), wherein the ER-retention signal is at the carboxy end of the complete, or a fragment of, the amino acid sequence of α-galactosidase, wherein said fragment of the amino acid sequence of α-galactosidase comprises a deletion of at the carboxy end of α-galactosidase, wherein said deletion is one to twenty-five amino acids. The present invention also provides for a polynucleotide encoding the aforementioned polypeptide. [0042]
  • The present invention also relates to the production of these human or animal lysosomal enzymes, including the aforementioned polypeptides, in transformed or transfected plants, plant cells or plant tissues, and involves constructing and expressing recombinant expression constructs comprising lysosomal enzyme coding sequences in a plant expression system. The plant expression system provides appropriate co-translational and post-translational modifications of the nascent peptide required for processing, e.g., signal sequence cleavage, glycosylation, and sorting of the expression product so that an enzymatically active protein is produced. Using the methods described herein, recombinant lysosomal enzymes are produced in plant expression systems from which the recombinant lysosomal enzymes can be isolated and used for a variety of purposes. [0043]
  • The present invention is exemplified by virally transfected and transgenic tobacco plants with lysosomal enzyme expression constructs. One construct comprises a nucleotide sequence encoding a modified human glucocerebrosidase (hGCB). Another construct comprises nucleotide sequence encoding a human α galactosidase (α gal or α gal A). Virally transfected and transgenic tobacco plants having the expression constructs produce lysosomal enzymes that are enzymatically active and have high specific activity. [0044]
  • The plant expression systems and the recombinant lysosomal enzymes produced therewith have a variety of uses, including but not limited to: (1) the production of enzymatically active lysosomal enzymes for the treatment of lysosomal storage diseases; (2) the production of altered or mutated proteins, enzymatically active or otherwise, to serve as precursors or substrates for further in vivo or in vitro processing to a specialized industrial form for research or therapeutic uses, such as to produce a more effective therapeutic enzyme; (3) the production of antibodies against lysosomal enzymes for medical diagnostic use; and (4) use in any commercial process that involves substrate hydrolysis.[0045]
    • BRIEF DESCRIPTION OF FIGURES
  • FIG. 1 shows a Tobamovirus expression vectors. [0046]
  • FIG. 2 shows a Tobamovirus expression vector containing the human ax galactosidase gene or a variant of the gene. The amino acid sequence of cCASP and Native SP depicted in FIG. 2 are depicted in SEQ ID. NO: 1 and 2, respectively. The entire amino acid sequence of WT rGAL-A is depicted in SEQ ID NO: 4. [0047]
  • FIG. 3A shows accumulation by Western Analysis of total plant soluble extract anti human GAL-A sera. [0048]
  • FIG. 3B shows activity of WT rGAL-A at 8 and 14+ days post inoculation of the plant host with a viral vector. [0049]
  • FIG. 4A shows Western blot analysis of total plant soluble extract anti human GAL-A sera [0050]
  • FIG. 4B shows activity of WT rGAL-wt and rGAL-wtR at 8 and 14+ days post inoculation of the plant host with a viral vector. [0051]
  • FIG. 5 shows carboxy terminal modifications to α galactosidase. The asterisk indicates a potential CTPP cleavage site according to Gene 58: 177, 1987. The entire nucleic acid and amino acid sequences of WT RGAL-A, WT-rGAL-AR, rGAL-4, rGAL-4R, rGAL-8, rGAL-8R, rGAL-12, rGAL-12R, rGAL-25, and rGAL-25R are depicted in SEQ ID NO: 3-22, respectively. [0052]
  • FIG. 6 shows western blot analysis of the accumulation of 10 carboxy-modified rGAL-A variants from interstitial fluid and from total plant homogenate. [0053]
  • FIG. 7 shows a comparison of enzymatic activity of the 10 carboxy-modified RGAL-A variants. [0054]
  • FIG. 8 shows a Coomassie blue stained electrophoresis gel separation of carboxy-modified rGAL-A variants and controls. [0055]
  • FIG. 9 shows a Coomassie blue stained electrophoresis gel separation of carboxy-modified rGAL-A variants and controls. [0056]
  • FIG. 10 shows a schematic representation of rGAL-A secretion from the endoplasmic reticulum to the apoplast. [0057]
  • FIG. 11 shows different glycosylation structures of α galactosidase. [0058]
  • FIG. 12 shows TTODA (rGAL-12R) TMV RNA begins at [0059] base 1; 126/183 reading frame begins at 69, 3417 is suppressible stop codon, and ends at 4919.30K ORF begins at 4903 and ends at 5709. Human a galactosidase A RNA begins at 5703, α amylase signal peptide is from 5762-5857; mature human α galactosidase A coding region is 5858-7036, ToMV virus coat protein and 3 UTR follows. (SEQ ID NO: 33)
  • FIG. 13 shows SBS5-rGAL-12R TMV RNA begins at [0060] base 1; 126/183 reading frame begins at 69, 3417 is suppressible stop codon, and ends at 4919.30K ORF begins at 4903 and ends at 5709. Human α galactosidase A RNA begins at 5703, complete (signal peptide and mature protein coding region) human α galactosidase A gene 5766-7037, TMV U5 virus coat protein and 3 UTR follows (SEQ ID. NO: 34).
  • FIG. 14 shows the construct within pBSG638: a dual [0061] Cauliflower Mosiac Virus 35S promoter linked to a translational enhancer from Tobacco Etch Virus linked 5′ to, and a polyadenylation region from the nopline synthase gene of Agrobacterium tumefaciens linked 3′ to, the native human GCB cDNA.
  • FIG. 15 shows the construct within pBSG641: a dual [0062] Cauliflower Mosiac Virus 35S promoter linked 5′ to, and a polyadenylation region from the nopline synthase gene of Agrobacterium tumefaciens linked 3′ to, the entire genome of Tobacco Mosaic Virus except the coat protein region is replaced with the GCB gene.
    • DETAILED DESCRIPTION OF THE INVENTION
  • The present invention provides a polynucleotide comprising the nucleotide sequence depicted in SEQ ID NO: 3, 5, 7, 9, 11, 13, 15, 17, 19, 31, or 32. The present invention also provides a polypeptide comprising the amino acid sequence depicted in SEQ ID NO: 4, 6, 8, 10, 12, 14, 16, 18, or 20. [0063]
  • The present invention further provides for a polypeptide comprising (a) the complete, or a fragment of, the amino acid sequence of α-galactosidase and (b) the amino acid SEKEL (SEQ ID NO:37), wherein SEKEL is at the carboxy end of the complete, or a fragment of, the amino acid sequence of α-galactosidase, wherein said fragment of the amino acid sequence of α-galactosidase comprises a deletion of at the carbozy end of α-galactosidase, wherein said deletion is one to twenty-five amino acids. Preferably, the deletion is one to twelve amino acids. More preferably, the deletion is four to twelve amino acids. The present invention further provides for a polynucleotide comprising a nucleotide sequence encoding the aforementioned polypeptide(s). [0064]
  • The present invention further provides for a polynucleotide encoding the aforementioned polypeptide(s). [0065]
  • The present invention also provides for a viral vector or expression vector comprising the aforementioned polynucleotide(s) or encoding the aforementioned polypeptide(s). The viral vector or expression vector is capable of expression and systemic expression of the polypeptide(s) encoded by the polynucleotide in a plant cell or a plant. Preferably, the viral vector or expression vector is derived from or based on or obtained from an RNA virus or an RNA viral vector. More preferably, the RNA virus is an RNA plant virus. Even more preferably, the RNA plant virus is a single-stranded plus-sense RNA plant virus. The RNA plant virus is multi-partite, monopartite, bipartite, tripartite, or the like. Even much more preferably, the single-stranded plus-sense RNA plant virus is a tobamovrius, such as a tobacco mosaic virus. [0066]
  • The present invention further provides for a plant cell or a plant expressing the aforementioned polypeptide(s). [0067]
  • The present invention provides for a method for producing a protein of choice comprising a lysosomal enzyme which is enzymatically active, comprising: recovering the lysosomal enzyme from (i) a transgenic plant cell or (ii) a cell, tissue or organ of a transgenic plant, which transgenic plant cell or plant is transformed or transfected with a recombinant expression construct comprising a nucleotide sequence encoding the lysosomal enzyme and a promoter that regulates expression of the nucleotide sequence so that the lysosomal enzyme is expressed by the transgenic plant cell or plant. [0068]
  • The promoter can be an inducible promoter. The inducible promoter can be induced by mechanical gene activation. The method can be carried out with the transgenic plant and additionally comprises a step of inducing the inducible promoter before or after the transgenic plant is harvested, which inducing step is carried out before recovering the lysosomal enzyme from the cell, tissue or organ of the transgenic plant. [0069]
  • The lysosomal enzyme can be a modified lysosomal enzyme which is enzymatically active and comprises: (a) an enzymatically-active fragment of a human or animal lysosomal enzyme; (b) the human or animal lysosomal enzyme or (a) having one or more amino acid residues added to the amino or carboxyl terminus of the human or animal lysosomal enzyme or (a); or (c) the human or animal lysosomal enzyme or (a) having one or more naturally-occurring amino acid additions, deletions or substitutions. The modified lysosomal enzyme can comprise a signal peptide or detectable marker peptide at the amino or carboxyl terminal of the modified lysosomal enzyme. The modified lysosomal enzyme can be recovered from (i) the transgenic plant cell or (ii) the cell, tissue or organ of the transgenic plant by reacting with an antibody that binds the detectable marker peptide. The antibody can be a monoclonal antibody. [0070]
  • The modified lysosomal enzyme can comprise: (a) an enzymatically-active fragment of an a-N-acetylgalactosaminidise, acid lipase, a-galactosidase, glucocerebrosidase, a-L-iduronidase, iduronak sulfatase, a-mannosidase or sialidase; (b) the a-N-a-cetylgalactosaminidase, acid lipase, a-galactosidase, glucocerebrosidase, a-L-iduronidase, iduronate sulfatase, a-mannosidase, sialidase or (a) having one or more amino acid residues added to the amino or carboxyl terminus of the a-N-acetylgalactosaminidase, acid lipase, a-galactosidase, glucocerebrosidase, a-L-iduronidase, iduronate sulfatase, a-mannosidase, sialidase or (a); or (c) the a-N-acetylgalactosaminidase, acid lipase, a-galactosidase, glucocerebrosidase, a-L-iduronidase, iduronate sulfatase, a-mannosidase, sialidasc or (a) having one or more naturally-occurring amino acid additions, deletions or substitutions. [0071]
  • The modified lysosomal enzyme can comprise: (a) an enzymatically-active fragment of a human glucocerebrosidase or human α-L-iduronidase enzyme; (b) the human glucocerebrosidase, human α-L-iduronidase or (a) having one or more amino acid residues added to the amino or carboxyl terminus of the human glucocerebrosidase, human α-L-iduronidase or (a); or (c) the human glucocerebrosidase, human α-Liduronidase or (a) having one or more naturally-occurring amino acid additions, deletions or substitutions. [0072]
  • The modified lysosomal enzyme can be a fusion protein comprising: (I) (a) the enzymatically-active fragment of the human or animal lysosomal enzyme, (b) the human or animal lysosomal enzyme, or (c) the human or animal lysosomal enzyme or (a) having one or more naturally-occurring amino acid additions, deletions or substitutions, and (II) a cleavable linker fused to the amino or carboxyl terminus of (I); and the method comprises: (a) recovering the fusion protein from the transgenic plant cell, or the cell, tissue or organ of the transgenic plant; (b) treating the fusion protein with a substance that cleaves the cleavable linker so that (1) is separated from the cleavable linker and any sequence attached thereto; and (c) recovering the separated (I). [0073]
  • The transgenic plant can be a transgenic tobacco plant. The lysosomal enzyme can be a human or animal lysosomal enzyme. The lysosomal enzyme can be an α-N-cetylgalactosaminidase, acid lipase, α-galactosidase, glucocerebrosidase, α-L-iduronidase, iduronate sulfatase, α-mannosidase or sialidese. The lysosomal enzyme can be a human glucocerebrosidase or human α-L-iduronidase. The organ can be a leaf, stem, root, flower, fruit or seed. [0074]
  • The present invention provides for a recombinant expression construct comprising a nucleotide sequence encoding a protein of choice comprising a lysosomal enzyme and a promoter that regulates the expression of the nucleotide sequence in a plant cell. [0075]
  • The promoter can be an inducible promoter. The inducible promoter can be induced by mechanical gene activation. The lysosomal enzyme can be a modified lysosomal enzyme which is enzymatically active and comprises: (a) an enzymatically active fragment of a human or animal lysosomal enzyme; (b) the human or animal lysosomal enzyme or (a) having one or more amino acid residues added to the amino or carboxyl terminus of the human or animal lysosomal enzyme or (a); or (c) the human or animal lysosomal enzyme or (a) having one or more naturally-occurring amino acid additions, deletions or substitutions. The modified lysosomal enzyme can comprise a signal peptide or detectable marker peptide at the amino or carboxyl terminal of the modified lysosomal enzyme. [0076]
  • The modified lysosomal enzyme can comprise (a) an enzymatically-active fragment of an α-N-acetylgalactosaminidase, acid lipase, α-galactosidase, glucocerebrosidase, α-L-iduronidase, iduronate sulfatase, α-mannosidase or sialidase; (b) the α-N-acetylgalactosaminidase, acid lipase, α-galactosidase, glucocerebrosidase, α-L-iduronidase, iduronate sulfatase, α-mannosidase, sialidase or (a) having one or more amino acid residues added to the amino or carboxyl terminus of the α-N-acetylgalactosaminidase, acid lipase, α-galactosidase, glucocerebrosidase, α-Liduronidase, iduronate sulfatase, α-mannosidase, sialidase or (a); or (c) the α-N-acetylgalactosaminidase, acid lipase, α-galactosidase, glucocerebrosidase, α-L-iduronidase, iduronate sulfatase, α-mannosidase, sialidase or (a) having one or more naturally-occurring amino acid additions, deletions or substitutions. [0077]
  • The modified lysosomal enzyme can comprise (a) an enzymatically-active fragment of a human glucocerebrosidase or human α-L-iduronidase enzyme; (b) the human glucocerebrosidase or human α-L-iduronidase or (a) having one or more amino acid residues added to the amino or carboxyl terminus of the human glucocerebrosidase, human α-L-iduronidase or (a); or (c) the human glucocerebrosidase, human (α-L-iduronidase or (a) having one or more naturally-occurring amino acid additions, deletions or substitutions. [0078]
  • The modified lysosomal enzyme can be a fusion protein comprising: (I) (a) the enzymatically-active fragment of the human or animal lysosomal enzyme, (b) the human or animal lysosomal enzyme, or (c) the human or animal lysosomal enzyme or (a) having one or more naturally-occurring amino acid additions, deletions or substitutions, and (II) a cleavable linker fused to the amino or carboxyl terminus of (I). The lysosomal enzyme can be a human or animal lysosomal enzyme. The lysosomal enzyme can be an α-N-acetylgalactosaminidase, acid lipase, α-galactosidase, glucocerebrosidase, α-L-iduronidase, iduronate sulfatase, α-mannosidase or sialidase. The lysosomal enzyme can be a human glucocerebrosidase or human α-L-iduronidase. [0079]
  • The present invention provides for a plant transformation or transfection vector comprising any of the recombinant expression construct recited above. [0080]
  • The present invention provides for a plant which is transformed or transfected with any of the recombinant expression construct recited above. [0081]
  • The present invention provides for a plant cell, tissue or organ which is transformed or transfected with any of the recombinant expression construct recited above. [0082]
  • The present invention provides for a plasmid comprising any of the recombinant expression construct recited above. [0083]
  • The present invention provides for a transgenic plant or plant cell capable of producing a lysosomal enzyme which is enzymatically active, which transgenic plant or plant cell is transformed or transfected with a recombinant expression construct comprising a nucleotide sequence encoding a lysosomal enzyme and a promoter that regulates expression of the nucleotide sequence in the transgenic plant or plant cell. The promoter is an inducible promoter. The inducible promoter is induced by mechanical gene activation. The lysosomal enzyme which is a modified lysosomal enzyme which is enzymatically active and which comprises: (a) an enzymatically-active fragment of a human or animal lysosomal enzyme; (b) the human or animal lysosomal enzyme or (a) having one or more amino acid residues added to the amino or carboxyl terminus of the human or animal lysosomal enzyme or (a); or (c) the human or animal lysosomal enzyme or (a) having one or more naturally-occurring amino acid additions, deletions or substitutions. The modified lysosomal enzyme comprises a signal peptide or detectable marker peptide at the amino or carboxyl terminal of the modified lysosomal enzyme. [0084]
  • The modified lysosomal enzyme comprises: (a) an enzymatically-active fragment of an α-N-acetylgalactosaminidase, acid lipase, α-galactosidase, glucocerebrosidase, α-L-iduronidase, iduronate sulfatase, α-mannosidase or sialidase; (b) the α-N-acetylgalactosaminidase, acid lipase, α-galactosidase, glucocerebrosidase, α-L-iduronidase, iduronate sulfatase, α-mannosidase, sialidase or (a) having one or more amino acid residues added to the amino or carboxyl terminus of the α-N-acetylgalactosaminidase, acid lipase, α-galactosidase, glucocerebrosidase, α-L-iduronidase, iduronate sulfatase, amannosidase, sialidase or (a); or (c) the α-N-acetylgalactosaminidase, acid lipase, α-galactosidase, glucocerebrosidase, α-L-iduronidase, iduronate sulfatase, α-mannosidase, sialidase or (a) having one or more naturally-occurring amino acid additions, deletions or substitutions. [0085]
  • The modified lysosomal enzyme can comprise: (a) an enzymatically-active fragment of a human glucocerebrosidase or human α-L-iduronidase enzyme; (b) the human glucocerebrosidase, human α-L-iduronidase or (a) having one or more amino acid residues added to the amino or carboxyl terminus of the human glucocerebrosidase, human α-L-iduronidase or (a); or (c) the human glucocerebrosidase, human a-L-iduronidase or (a) having one or more naturally-occurring amino acid additions, deletions or substitutions. [0086]
  • The modified lysosomal enzyme is a fusion protein comprising: (I) (a) the enzymatically-active fragment of the human or animal lysosomal enzyme, (b) the human or animal lysosomal enzyme, or (c) the human or animal lysosomal enzyme or (a) having one or more naturally-occurring amino acid additions, deletions or substitutions, and (II) a cleavable linker fused to the amino or carboxyl terminus of (I). The transgenic plant or plant cell is a transgenic tobacco plant or tobacco cell. The lysosomal enzyme is a human or animal lysosomal enzyme. The lysosomal enzyme is an a-N-acetylgalactosaminidase, acid lipase, a-galactosidase, glucocerebrosidase, a-L-iduronidase, iduronate sulfatase, a-mannosidase or sialidase. The lysosomal enzyme is a human glucocerebrosidase or human a-L-iduronidase. [0087]
  • The present invention provides for a leaf, stem, root, flower or seed of any of the transgenic plant recited above. [0088]
  • The present invention provides for a seed of plant line Nicotiana sp., which seed has the ATCC Accession No. PTA-2258, deposited Jul. 25, 2000. [0089]
  • The present invention provides for a plant grown from the seed recited above. [0090]
  • The present invention provides for a lysosomal enzyme which is enzymatically active and is produced according to a process comprising: recovering the lysosomal enzyme from (i) a transgenic plant cell or (ii) a cell, tissue or organ of a transgenic plant which transgenic plant cell or plant is transformed or transfected with a recombinant expression construct comprising a nucleotide sequence encoding the lysosomal enzyme and a promoter that regulates expression of the nucleotide sequence so that the lysosomal enzyme is expressed by the transgenic plant cell or plant. The promoter can be an inducible promoter. The process is carried out with the transgenic plant and additionally can comprise a step of inducing the inducible promoter before or after the transgenic plant is harvested, which inducing step is carried out before recovering the lysosomal enzyme from the cell, tissue or organ of the transgenic plant. [0091]
  • The modified lysosomal enzyme which can be enzymatically active and can comprise: (a) an enzymatically-active fragment of a human or animal lysosomal enzyme; (b) the human or animal lysosomal enzyme or (a) having one or more amino acid residues added to the amino or carboxyl terminus of the human or animal lysosomal enzyme or (a); or (c) the human or animal lysosomal enzyme or (a) having one or more naturally-occurring amino acid, additions, deletions or substitutions. The modified lysosomal enzyme can comprise a signal peptide or detectable marker peptide at the amino or carboxyl terminal of the modified lysosomal enzyme. [0092]
  • The modified lysosomal enzyme can comprise: (a) an enzymatically-active fragment of an α-N-acetylgalactosaminidase, acid lipase, α-galactosidase, glucocerebrosidase, α-L-iduronidase, iduronate sulfatase, α-mannosidase or sialidase; (b) the α-N-acetylgalactosaminidase, acid lipase, α-galactosidase, glucocerebrosidase, α-Liduronidase, iduronate sulfatase, α-mannosidase, sialidase or (a) having one or more amino acid residues added to the amino or carboxyl terminus of the α-N-acetylgalactosaminidase, acid lipase, α-galactosidase, glucocerebrosidase, α-L-iduronidase, iduronate sulfatase, amannosidase, sialidase or (a); or (c) the α-N-acetylgalactosaminidasd, acid lipase, α-galactosidase, glucocerebrosidase, α-L-iduronidase, iduronate sulfazase, α-mannosidase, sialidase or (a) having one or more naturally-occurring amino acid additions, deletions or substitutions. [0093]
  • The modified lysosomal enzyme comprises: (a) an enzymatically-active fragment of a human glucocerebrosidase or human α-L-iduronidase enzyme; (b) the human glucocerebrosidase, human α-L-iduronidase or (a) having one or more amino acid residues added to the amino or carboxyl terminus of the human glucocerebrosidase, human α-L-iduronidase or (a); or (c) the human glucocerebrosidase, human α-L-iduronidase or (a) having one or more naturally-occurring amino acid additions, deletions or substitutions. The modified lysosomal enzyme can be a fusion protein comprising: (I) (a) the enzymatically-active fragment of the human or animal lysosomal enzyme, (b) the human or animal lysosomal enzyme, or (c) the human or animal lysosomal enzyme or (a) having one or more naturally-occurring amino acid additions, deletions or substitutions, and (II) a cleavable linker fused to the amino or carboxyl terminus of (I). [0094]
  • The transgenic plant can be a transgenic tobacco plant. The lysosomal enzyme can be a human or animal lysosomal enzyme. The lysosomal enzyme can be an α-N-acetylgalactosaminidase, acid lipase, α-galactosidase, glucocerebrosidase, α-L-iduronidase, iduronate sulfatase, α-mannosidase or sialidase. The lysosomal enzyme can be a human glucocerebrosidase or human α-L-iduronidase. The organ can be a leaf, stem, root, flower, fruit or seed. [0095]
  • Gal-A is one of many proteins that require glycan site occupancy at N-linked sites to achieve proper folding and stability. The ability to successfully target the enzyme in Fabry patients is also likely to be glycosylation-dependent. This requirement presently limits the expression possibilities to eukaryotic cell types. Recombinant proteins synthesized in baculovirus and yeast expression systems are often hyperglycosylated and highly heterogeneous complicating the preparation of therapeutically effective glycoforms from these sources. The rGal-A synthesized in plants is a relatively homogeneous glycoform as analyzed by its SDS-PAGE electrophoretic mobility and comigrates with rGal-A produced purified from placenta (FIG. 3). The expression results (yield and purity) we have already presented are unprecedented in any eukaryote system for a glycosylated enzyme and are not likely to be achieved in the foreseeable future with transgenic plants or animals. “Crude” rGal-A from the leaf IF has a specific activity of over 1,000,000 U/mg of protein, whereas CHO, COS-1 and insect cell extracts and supernatants are maximally only 10-20,000 U/mg; (36,41,42). [0096]
  • Protein pharmaceuticals may vary over five orders of magnitude in unit value and be required in kg/year quantities. The example of Gaucher disease emphasizes the need progress in production phase research. Many additional heritable metabolic disorders, particularly those caused by dysfunctional lysosomal enzymes, might be treated by supplementation with exogenously produced enzymes. Enzyme replacement using macrophage-targeted human glucocerebrosidase has been shown to be extraordinarily beneficial for Gaucher patients. However, the cost of this treatment is very great. If the significant advances in clinical research are to be applied on a practical scale, new production technologies will be required to deliver bioproducts such as these to those in need at an affordable cost (43). No savings in Gaucher treatment costs were realized upon introduction of the recombinant CHO-cell product Cerezyme™ to replace the placental-derived Ceredase™. A significant reduction in cost requires fundamental changes in both the source of enzyme and process of purification. [0097]
  • While the existing treatment for Gaucher disease is safe and effective, there are potential contaminants derived from the source material that may pose serious risks. For the existing pharmaceutical products, these risks primarily include possibilities of contamination with human pathogenic viruses or peptides with potent hormonal activities such as human chorionic gonadotropin (44). These potential contaminants are not present in plant source material. [0098]
  • The main goal in selecting plants for expression of this protein is the potential for a radical reduction in costs. For the RNA-viral mediated synthesis of rGal-A and rGCB in plants, this is very likely to be achieved through the synergistic combination of three factors: [0099]
  • Complex crude extracts from various eukaryote cell production systems may be replaced with a plant leaf homogenate or IF fractions highly enriched in recombinant product. [0100]
  • Large-scale, sterile, cell fermentation systems and associated media, capitalization, and waste costs may be replaced with plant biomass. Production is then inexpensively scaled to the quantities desired. [0101]
  • The labor and time required to generate transgenic higher plants or animals may be replaced with a very rapid and simple plant transformation or plant viral transfection system. [0102]
  • Modern agriculture can supply a new generation of medicinal plants as a source of pharmaceuticals—a source that should be as inexpensive and readily available as our food, fiber, flavors and chemical feedstocks. [0103]
  • Experimental Design and Methods [0104]
  • Post-Translational Processing and Secretion. Protein secretion to the plant apoplast is through a default pathway. In our experience, addition of the rice α-amylase signal peptide (α-ASP) sequence at the N-terminus of several recombinant proteins is sufficient to direct the protein to the lumen of the ER in tobacco leaves. However, this is not likely to be a rate-limiting step in protein accumulation and many native signal peptides may function equally well in plants. It would be most desirable to include few if any additional AA residues at the N terminus after processing. For this reason, we compared expression from the native signal peptide encoded in human Gal-A cDNA to that from the foreign α-ASP sequence. [0105]
  • Mutations in the carboxy-terminal domain of the Gal-A homodimer have profound effects on enzymatic activity. Several mutations occurring in individuals affected with Fabry disease map to this region. Some of these mutations have a dominant negative phenotype. When a peptide map was published on Gal-A purified from human lung, the authors noted the absence of the most carboxy-terminal predicted fragment and hypothesized the proteolytic removal of 26 or 28 AA from this region (39,40). Very recently Miyamura et al. published a study of the effects of carboxy-terminal truncations on enzymatic activity in transfected COS-1 cells (42). Between 2 and 17 AA residues were removed by introducing stop codons into a series of cDNA constructs. Relative enzyme activity, measured using 4-MUG as a substrate, first increased and then decreased as AA were removed. 12 and 17 AA constructs had no activity, while 11 was the same as wild type. A 4 AA construct yielded the highest activity at approximately 6.2× the full-length sequence. Because the precise AA sequence of the carboxy-terminus of the native human enzyme was never determined, there is insufficient information to interpret these results. The carboxy-terminal domain may affect the conformation of the active site either directly or indirectly through a proteolytic maturation step and/or assembly and subcellular localization of the active form. Furthermore, it is important to stress that it is the enzyme activity on galactose-terminal glycosphingolipids that is relevant to development of a therapeutic enzyme. [0106]
  • Plant proteins do not require N-linked oligosaccharides for correct sorting into vacuoles (35,37,38). Some vacuolar proteins (osmotin, thaumatin, chitinase-I, glucanase-I and a barley lectin), contain sorting information in a CTPP of 7 to 22 AA in length. For several of these proteins secreted isoforms are synthesized without a CTPP domain. In other cases, experimental deletion of the CTPP results in secretion of the recombinant protein to the IF (45-48). Sorting of Gal-A to the lysosome is likely to occur by the well-characterized mannose-6-phosphate receptor pathway in mammalian cells. We hypothesize that a redundant sorting signal may exist in this carboxy-domain that also serves to reduce enzymatic activity in the ER lumen, golgi and trans-golgi network. This signal appears to function in plant cells, presumably for vacuolar localization. [0107]
  • Scale-up Purification and Analysis. In order to evaluate the performance of larger scale process equipment, we designed and had built a custom basket centrifuge fixture for a laboratory low-speed centrifuge that has a capacity of approximately 1 kilogram leaf material. The sensitivity of the fluorescent 4-MUG enzyme assay allowed us to begin to evaluate enzyme purification from the leaf IF fraction using the construct rGal-A-SEKDEL. (This vector only yields approximately {fraction (1/50)}th the activity of rGal-A12-SEKDEL). Leaf tissue was transfected, harvested and infiltrated as described in Section B4 (Experimental Results). Galactosidase activity was stable in crude IF extracts and was bound to the hydrophobic interaction resin octyl sepharose, and eluted in a descending ammonium sulfate gradient. The lectin resin concanavalin-A sepharose was also effective, indicating the presence of at least one high mannose chain. The enzyme did not bind to a commercially available melibiose column (Sigma). [0108]
  • We have measured the enrichment provided by the affinity resin α-galactosylamine Sepharose with a C12 arm (49). Some or all of the three effective chromatography steps were combined as necessary with a size exclusion fractionation to yield highly purified enzyme(s). Some or all of the three effective chromatography steps were comined as necessary with a size exclusion fractionation to yield highly purified enzyme(s). Because our current source of enzyme is so enriched (FIG. 3), and several of the published purification steps we have shown to be compatible with the plant IF extracts, we anticipate no problems in enzyme purification. Pure enzyme preparations were shipped to the laboratory of Drs. Roscoe Brady and Gary Murray for evaluation of enzyme activity with [0109] 14C-galactose-labeled ceramide trihexoside. These colleagues were responsible for the development of the therapeutically effective glycoform of glucocerebrosidase used to treat Gaucher disease.
  • We scaled up the purification of up to four candidate therapeutic enzymes as necessary in our indoor greenhouses. In our initial experiment, 38 and 48 percent of the total rGal-A activity was recovered upon the first infiltration and centrifugation treatment (Construct rGal-A12-SEKDEL) for a yield of >50 mg of enzyme per kilogram of leaf material. Experience with the extraction of glucocerebrosidase from the IF indicates that additional enzyme is recovered in a second treatment. In these experiments one leaf was collected for each sample from each of two plants. There was considerable plant to plant variation in the level of enzyme activity (Table 1). We analyzed more carefully the accumulation of enzyme activity over time post-inoculation to optimize yields. Our facilities are more than sufficient to provide the 1 kilogram quantities of biomass necessary to purify nanomoles of enzyme for the following sequence and structural work. Sequence analysis and MALDI-TOF molecular weight determination was performed as a commercial service by Commonwealth Biotechnologies, Inc. N-terminal sequence is by the automated Edman degradation. C-terminal sequence is by carboxypeptidase digestion followed with amino acid analysis. [0110]
  • Full-Scale Bioprocess Pilot Plant [0111]
  • Macroextraction. Large-scale maceration of tissue was accomplished by a 65 hp Rietz disintegrator mill. The macerated tissue was then separated into a “green juice” fraction and a fiber fraction in a Rietz screw press. The fiber fraction was dried in a Cardwell drier. The “green juice” was then pH adjusted and heated in a dual plate-and-frame heat exchanger system with adjustable holding tube. The process of pH adjustment and heating causes the precipitation of the F1 protein complex. The protein was then clarified in a 40 hp. Westphalia SA-40 disk stack centrifuge capable of clarification of “green juice” at greater than 20 gallons per minute (GPM). [0112]
  • Downstream Processing. The concentrate was then pumped to [0113] Clean Room 1 that houses the primary ultrafiltration (UF) equipment. This equipment was fitted with over 1000 sq. ft. of spiral wound membranes. Typically, the UF was equipped with 100,000 kDa cut-off membranes. Virus particles are recovered in the retentate. Lower molecular weight proteins are recovered in the permeate. The permeate was fractionated by a second UF system fitted with appropriate molecular weight cut-off membranes. The retentate was processed in Clean Room 2. Virus was recovered by polyethylene glycol (PEG) precipitation and centrifugation in two Sharples vertical bowl centrifuges. Final purification of soluble proteins and peptides was accomplished on a series of chromatography systems.
  • Additional Facilities. The facility has other major unit processes available for the recovery and purification of plant fractions. There are two Alar diatomaceous earth, rotary vacuum filters. One of the filters was in an explosion proof area of the pilot plant that can be used for solvent extraction. The solvent extraction facility also has a biphasic solvent extractor and high efficiency distillation column. Extensive tankage was available both indoors and outdoors. Pumps, filters and other process equipment are available at the facility, allowing a large margin of flexibility while developing new processes. [0114]
  • Full-Scale Pilot Plant Implementation. The Bioprocess Facility has excellent supporting infrastructure. The 900 square foot laboratory was equipped with all the basic tools for biochemical and protein analyses including: electrophoresis, gel filtration, HPLC, spectrophotometry, basic chromatography, chemical analysis, and sample preparation and preservation. The full scale pilot plant has approximately 15,000 square feet of additional floor space for expansion including a high bay tower. External solvent tanks are placed in diked enclosures. Two rapid recovery, high pressure (up to 600 psi) steam generators and a large twin screw, oilless compressor are on site. A complete shop and maintenance facility was present along with walk-in cold room and walk-in freezer. Additional equipment includes a ceramic microfiltration system, a spray dryer and an array of tanks, pumps, filters, heat exchangers, and agitators. [0115]
  • Process equipment was fabricated and modified by a group of skilled vendors and craftsmen capable of fabricating specialized equipment designed by the company, and has excellent field experience working in large scale operations. [0116]
  • Infiltration System. Vacuum infiltration can be accomplished in the field or at the processing facility. Development experiments determine the necessity to infiltrate the material in the field. A vacuum tank was used as the receiver for the plant tissue after harvest by the tobacco cutter. The tissue was conveyed into a trailer-mounted tank capable of full vacuum and slurried into an infiltration buffer. The Owensboro facility has a trailer capable of carrying approximately 18,000 lb. This will translated into approximately 1,000 gallons per trip to the field. The trailer was fitted with a 2,000 gallon tank capable of full volume and evacuated by a gasoline driven vacuum pump. In harvests from 1991-1994, it was the goal of the team to have harvested biomass at the processing facility in less than 1 hour after cutting. If the tissue can be held for approximately one hour without significant loss of enzyme activity, the biomass can be brought from the field in the conventional wagon and infiltrated at the processing facility. Several large, full vacuum tanks can be employed at the facility to increase the total throughput of the plant. Two large-scale vacuum pump systems in the plant that are currently associated with the Alar rotary vacuum filters can be used for the vacuum infiltration process step. [0117]
  • Basket Centrifugation. The full-scale basket-type centrifuge was a discontinuous batch-type system. Leaf tissue can be slurried in, dewatered as a batch, then a scraper system discharges the solids to a bottom dump. Large leaves and pieces of tissue can be handled in this manner. The potential of placing a vacuum system on the discharge side of the centrifuge was also be investigated. The centrifuge was a hydraulically driven conventional basket centrifuge with a bottom discharge and bowl dimension of 48 inches in diameter and a depth of 30 inches. Optimum loadings of the centrifuge in full-scale was determined the throughput and cycle times of this process step. [0118]
  • Vacuum Extraction. Vacuum extraction can be accomplished in large-scale by a web or belt-type vacuum filter system common in the food ingredient business. The “in-plant” vacuum systems could also be adapted to operate this type of filter. The plant tissue can be placed on this type of filter before or after the centrifugation step. Some damage of the biomass was anticipated during the scraper mediated discharge of the basket centrifuge. The discharged material was analyzed for the presence of intracellular components and their effect on enzyme activity, recovery and separation. These data determined the position of the vacuum filtration step in the process flow. [0119]
  • Downstream Processing. The initial UF separation was accomplished by an Alfa-Laval custom UF system consisting of six modular housings each containing either three 12 inch spiral wound membranes (Amicon type) or one standard 38 inch module. This yields a UF system with between 740 and 1140 square feet of membrane area of typical spiral wound configuration. The ability to interchange housings and replace housings by spool pieces gives the system great flexibility in large-scale process development. This system was housed in [0120] Clean Room # 1. This room is 14×18 ft, and is under positive pressure, HEPA-filtered air. A second UF system was available in Clean Room #1. This smaller system, built by Separations Equipment Technology (SETEC), has the capacity for 320 square feet of spiral wound membrane. This system was employed for the second separation and diafiltration. It was designed for automatic diafiltration. Clean Room # 2 is equipped with a Pharmacia Streamline fluid bed gel filtration system equipped with UV and refractive index monitoring equipment. This unit was available for chromatography steps.
  • An antiserum specific for these xylose- and fucose-containing complex glycans was especially useful in developing an ELISA assay to follow enzymatic deglycosylation. Large quantities of purified enzyme facilitate definitive determination of glycosylation structure and if necessary provide adequate rGal-A to use as substrate for enzymatic deglycosylation reactions. Using Gal-A knockout mice in the laboratory of Dr. Brady at NIH was an important genetic tool in developing a therapeutically effective glycoform. We use our transfected plants as a convenient source of recombinant enzyme for glycan analysis. Glycoforms are shown in FIG. 11. [0121]
  • Plants as a Source of Recombinant Pharmaceutical Proteins. A number of genetic tools have been developed during the last decade for the expression of foreign genes in plants. In addition to various antibody molecules (21-23), the accumulation of serum proteins (24) and candidate vaccine products (25-28) has been described in the leaves and other tissues of whole plants. We increased the attainable expression levels through the use of chimeric RNA viruses. For production of specific proteins, transient expression of foreign genes in plants using virus-based vectors has several advantages. These chimeric viruses move quickly from an initial infection site and deliver the recombinant gene to essentially all somatic cells of the plant. The gene vectors are premier analytical tools because they allow both high level expression and brief cycles of protein modification and testing. A permissive host provides high levels of expression and may be used for rapid, large-scale recombinant protein production in whole plants. [0122]
  • We validated the performance of plant-based expression systems for the production of recombinant proteins and peptides of pharmaceutical significance. In two weeks post-inoculation, the ribosome inactivating enzyme α-trichosanthin was over-produced in plants to 2% of the total soluble protein and had the same specific activity as the enzyme from the native source (29). Because these products can be obtained from a non-sterile, low input, renewable and easily scalable source, the costs of synthesis in plants are negligible. We confirmed the performance and containment of the vectors in four field trials (1991, 1994, 1995, 1996). [0123]
  • The vectors of the invention are based on chimeras between the 6.4 kb single-stranded RNA genome of tobacco mosaic virus (TMV) and other members of the tobamovirus group. Most of the TMV genome encodes overlapping reading frames required for replication and transcription (FIG. 1A). These are located at the 5′ end of the virus and translated from genomic RNA yielding proteins of 126 and 183 kDa. Expression of the internal genes was controlled by different promoters on the minus-sense RNA that direct synthesis of 3′-coterminal subgenomic mRNAs produced during replication. The 30 kDa protein, which was required for the virus to move from cell to cell, was produced early and in relatively low amounts, whereas the 17.5 kDa coat protein was produced late and usually as the most abundant protein in infected cells. Largely because of the strength of the coat protein subgenomic promoter, during peak protein synthesis the coat protein can be produced at up to 70% of the total rate of cellular protein synthesis without appreciably reducing host protein synthesis (30). [0124]
  • The entire cDNA of the TMV genome was cloned behind a bacterial phage promoter in an [0125] E. coli plasmid. Precise replicas of the virion RNA can be produced in vitro with RNA polymerase and dinucleotide cap, m7GpppG. This not only allows manipulation of the viral genome for reverse genetics, but it also allows manipulation of the virus into a gene transfer vector. Subgenomic promoters from divergent viral strains can be added to the genome to direct the expression of foreign genes. Enormous quantities of mRNA are synthesized and delivered directly from the cytoplasm to the ribosome. TMV-based transient vectors offer significant advantages over integration of genes into plant chromosomes. By altering the molecular exclusion limits of the cellular junctions between adjacent plant cells, the vector invades virtually every cell of the plant during a period of 2 weeks post-inoculation. For many gene products, the recombinant protein accumulates to several percent of the total protein during this brief period of time. In contrast, it was very time consuming and labor intensive to generate, select, and breed transgenic plants for recombinant protein production. Many of these selections were culled because of poor expression due to position effects or gene silencing phenomena. In many more lines, the levels of product accumulation was too low for development of a viable commercial process.
    • EXAMPLE 1
  • We have established that a recombinant human lysosomal enzyme (rGCB) synthesized in transgenic tobacco has comparable activity to the same enzyme isolated from other native and recombinant sources. We also investigated the feasibility and economic advantages of purifying large quantities of active rGCB from plants. We designed and fabricated laboratory equipment that enabled us to optimize the key initial steps of a purification process in the laboratory using kilogram quantities of biomass from our greenhouses. We standardized a series of assays for secretory and intracellular marker enzymes in addition to rGCB assays that allowed us to monitor both lab and field expression as well as the purification process. Leaf tissue was infiltrated with a suitable extraction buffer while submerged in a large vacuum chamber, allowing the solution to reach the leaf intercellular fluid containing rGCB. The IF fraction was recovered by centrifugation in a custom collection chamber and “basket” centrifuge rotor compatible with a conventional Beckman J2-2 1 spindle. rGCB was trapped from the dilute IF solution by expanded bed adsorption chromatography using a hydrophobic resin and eluted with polyethylene glycol. A second ion exchange chromatography step was implemented for an overall yield of 1.7 mg/kg at 41% purity to this stage. These procedures were then scaled-up to 100 kg during several pilot-process experiments in a field trial using analogous industrial bioprocess equipment. These results are summarized in the table below. Three lots of rGCB were further purified by RP-HPLC and used for carbohydrate profiling and composition analysis. In NMR experiments we confirmed that the GCB from the plant IF contains an N-linked glycan previously reported to occur in glycoproteins isolated from plant seeds and tissue cultures. This type of chain contains the plant-specific carbohydrate linkages of α 1-2 xylose and β 1-3 fucose on the trimannosyl core. [0126]
  • Making Transgenic Tobacco Plants to Produce Glucocerebrosidase [0127]
  • Several founder plant lines for genetically stable expression of rGCB were generated and characterized. Under greenhouse conditions individual plants accumulate rGCB to at least 1.3% of the total protein in the leaf intercellular fluid as estimated from enzymatic assays. This represents a 50-fold enrichment relative to the crude lysosomal fraction of placental extracts used as the starting material for the product Ceredase™. [0128]
  • Transgenic Tobacco Leaves Express Moderate Levels of rGCB. We combined a dual promoter from Cauliflower Mosaic Virus (35S), a translational enhancer from Tobacco Etch Virus and a polyadenylation region from the nopaline synthetase gene of [0129] Agrobacterium tumefaciens with the native human GCB cDNA to create plasmid pBSG638 (33; FIG. 14). These expression elements are widely used to provide the highest possible constitutive expression of nuclear encoded genes. Depending on the nature of individual proteins, these vectors can be used to accumulate moderate levels of recombinant proteins in most tissues of many plant species.
  • Using a standard Agrobacterium-mediated transformation method, we regenerated 93 independent kanamycin-resistant transformants from leaf discs of four different tobacco cultivars (the T0 generation). In Western blots of total protein extracts, cross-reacting antigen was detected in 46 of these T0 individuals with antibody raised against human glucocerebrosidase. Specificity of the plant-expressed recombinant enzyme was confirmed by hydrolysis of [0130] 14C-radiolabeled glucosylceramide.
  • Leaf Disc Transformation with [0131] Agrobacterium tumefaciens (59, 60, 61) Method:
  • 1) Transform the T-DNA plasmid into A.t. LBA4404 selecting for the bacterial Ab[0132] R gene (generally Km at 100 ug/ml).
  • 2) Pick a single colony into YEB medium plus antibiotic and grow at 28° C. overnight (to saturation; often takes a little longer than overnight). [0133]
  • 3) Take aseptic or surface-sterilized Nicotiana tabacum (MD609, Xanthi, SR1, Samsun) leaves, remove midrib and cut into leaf“chunks” ˜1 cm[0134] 2.
  • 4) With sterile forceps, dip (submerge) the leaf disc into the Agrobacterium suspension. [0135]
  • [0136]
    Figure US20040234516A1-20041125-P00001
    Placing the bacterial culture into a small petri dish is convenient.
  • 5) Remove the leaf disc from the Agrobacterium and place the disc on regeneration medium. Place the discs so that the underside of the leaf is up. (They seem to do better this way, perhaps because of better gas transfer.) [0137]
  • [0138]
    Figure US20040234516A1-20041125-P00001
    Use needle-nose forceps to handle the discs, thus introducing small puncture wounds into which Agrobacterium can infect; small wounds are good, major damage (e.g., crushing) to the disc is bad.
  • 6) Seal plate containing discs with Parafilm® and incubate at 25-28° C., preferably in light with a yellow filter to inhibit UV degradation of the medium. [0139]
  • 7) After 2 days co-incubation, transfer the leaf discs to selective plates (regeneration medium plus 500 ug/ml Cefotaxime). [0140]
  • 8) After 2 more days, transfer discs to regeneration medium plus 500 ug/ml cefotaxime and 100 ug/ml kanamycin [0141]
  • 9) When normal-looking shoots appear, excise them, taking care not to excise any callus, and place in rooting medium. [0142]
  • [0143]
    Figure US20040234516A1-20041125-P00001
    Callus on the end of the stem generally prevents rooting, and could lead to a chimeric set of shoots.
  • [0144]
    Figure US20040234516A1-20041125-P00001
    The lower % agar makes it easier to wash the agar off the roots when transferring to soil.
  • [0145]
    Figure US20040234516A1-20041125-P00001
    If there is time, it is a good practice (when the plants are rooted and growing) to cut the shoots off and re-root them. Escapes will generally not root on Km medium.
  • 10) When roots first appear, remove plantlets, wash agar from the roots and plant in soil medium in small pots. Cover pots with a plastic bag for the first 5 days or so to retain humidity and reduce transplantation shock. [0146]
  • 1 Liter of Regeneration Medium contains: [0147]
  • MS Salts [0148]
  • 30 g sucrose [0149]
  • 1 ml of 0.5 mg/ml nicotinic acid [0150]
  • 1 ml of 0.5 mg/ml pyridoxine HCl [0151]
  • 2 ml of 0.5 mg/ml thiamine HCl [0152]
  • 2 ml of 50 mg/ml inositol [0153]
  • 1.5 ml of 0.1 mg/ml IAA [0154]
  • 5.0 ml of 1.0 mg/ml 2-IP-2-iminopurine [0155]
  • 8 g of agar, pH 6.0 [0156]
  • 1 Liter of Rooting Medium contains: [0157]
  • ½×MS Salts [0158]
  • 10 g sucrose [0159]
  • 2 ml of 0.1 mg/ml IAA [0160]
  • 8 g agar, pH 5.7 [0161]
  • A deposit at ATCC under the Budapest treaty was made on Jul. 25, 2000 of seed from Nicotiana benthamiana MD609, Accession No. PTA-2258. [0162]
  • According to these expression results the rGCB positive transformants were ranked into moderate (A), low (B) and negligible (C) activity groups (Table 1). [0163]
    TABLE 1
    EXPRESSION OF rGCB IN THE T0 GENERATION
    Number of Specific Activity
    Group Individuals Units/mg
    A 13 130-390
    B 20  70-130
    C 13 24-68
    Controls  8  0-10
  • Specific Activity is based on hydrolysis of [14C]-glucosylceramide (Units=nmol/hr). [0164]
  • Plant rGCB is Similar to Macrophage-Targeted Glucocerebrosidase. We found reaction conditions to preferentially inhibit rGCB enzyme activity in the presence of plant glucosidases using the suicide substrate conduritol B-epoxide (CBE). Total glucosidase activity, and rGCB activity were measured by hydrolysis of the fluorescent substrate 4-methylumbelliferylglucopyranoside (4-MUG) with and without CBE. Total protein was determined by the method of Bradford. Detergents are necessary to solubilize and stabilize activity of this membrane-associated enzyme. Using a small scale (˜100 mg fresh weight) extraction procedure, several detergents were compared for yield of enzyme activity and purity (including; IGEPAL CA-630, Tween-20, Tween-80, Triton X-100, Triton X-114, CHAPS, taurocholic acid, cholic acid, deoxycholate and taurodeoxycholate). Buffer without detergent, deoxycholate, taurocholate and cholate below their critical micelle concentrations (CMC) (0.1%) yielded low units of rGCB. All of the other detergents gave comparable specific activity and yields of total activity with Tween-80 yielding slightly higher activity. The dialyzable bile salt, sodium taurocholate and the lower CMC detergent Tween-80 were compared at a range of concentrations (0.1-1% and 0.001-1%, respectively). Tween-80 at 0.15% and taurocholate at 0.5% gave the best yield and purity. [0165]
  • A number of chromatography steps were evaluated for purification of rGCB from total homogenates (Table 1). As is the case for the native placental enzyme, hydrophobic resins provide the most significant purification gains. Gel filtration, Con A Sepharose and affinity chromatography also worked very well, but some of these approaches may be impractical on a large scale. Both anion and cation chromatography may prove useful, but the ideal buffer conditions for stabilization of enzyme activity remain to be determined. [0166]
    TABLE 2
    SUMMARY OF CHROMOTOGRAPHY RESULTS
    Column Matrix Type Results
    Octyl Sepharose
    4 FF Hydrophobic +
    Phenyl Sepharose HP Hydrophobic +
    Phenyl Sepharose 6 FF Hydrophobic +
    Butyl Sepharose 4 FF Hydrophobic −
    Alkyl Superose Hydrophobic −
    SP Sepharose FF Strong Cation +/−−
    Q Sepharose FF Strong Anion +/−−
    Con A Sepharose Lectin Affinity +/−
    NHS-Activated Sepharose HP Antibody Affinity +
    Sephacryl S-100 HR Gel Filtration +
  • The post-translational processing of native glucocerebrosidase (GCR) in human cells is complex. Two primary translation products are derived from two in-phase start codons. These precursors, a 2:1 mixture of 60 kDa and 57 kDa proteins, are proteolytically processed to 55 kDa as they pass into the lumen of the ER. High mannose and complex glycans are subsequently added in the ER and Golgi compartments to yield 62 and 66 kDa glycoforms. Finally, exoglycosidases generate a mature 59 kDa lysosomal enzyme. Recall that glycosylation is required for both enzymatic activity and lysosomal targeting of transfused enzyme. Sialic acid, galactose, and N-acetylglucosamine residues are enzymatically removed in vitro by the sequential action of glycosidases to prepare glucocerebrosidase for therapy. The core pathway for biosynthesis and processing of N-linked complex glycans in plants appears identical to that found in animals. There are three known differences which occur later in the pathway. Sialic acid is not reported in complex glycans from plants, and the α1-3 fucose and β1-2 xylose linkages are unique (34). As analyzed by SDS/PAGE, rGCB has an apparent molecular weight of 59 kDa, and comigrates with the mannose-terminal therapeutic glycoform. We have not yet detected a significant shift in mobility upon treatment with glycosidases (PNGase F, Endo H, α 1-3 filcosidase) in our preliminary glycosylation analysis. However, the enzyme has an apparent molecular weight increase of 4 kDa over the proteolytically processed and unglycosylated form (55 kDa) and must be glycosylated for activity. Additional digestions are in progress with a more extensive set of endo- and exoglycosidases and known plant glycoprotein controls. N-Glycosidase A is reported to hydrolyze all types of N-glycan chains from glycopeptides and glycoproteins. [0167]
  • The signal peptide of rGCB is processed at the correct site. A very small quantity of protein was prepared for sequence analysis by purification through Phenyl-Sepharose, ConA-Sepharose and RP-HPLC to produce a single band on SDS-PAGE comigrating with authentic glucocerebrosidase. The sequence obtained was consistent with the known sequence of processed GCR (Table. 3). In this particular analysis, the first two positions were not resolved because some degradation occurred during sample preparation. Correct proteolytic cleavage of a signal peptide is also confirmed for a mouse antibody light chain molecule expressed in tobacco leaves (35). [0168]
    TABLE 3
    STRUCTURE OF THE N-TERMINUS OF rGCB
    N-terminal Amino Acid Sequence
    XXPXIPKSFGY rGCB from tobacco (SEQ ID NO: 35)
    ARPCIPKSFGY GCR human (SEQ ID NO: 36)
  • Plant rGCB Accumulates in the Leaf Intercellular Fluid. We localized rGCB to the intercellular fluid of the leaf using the following simple experimental design. Leaves were removed from the plant at the petiole and slit down the midrib into two equal halves. To obtain a total cellular homogenate, one group of half-leaves was ground in the presence of 4 volumes of detergent extraction buffer (100 mM [0169] potassium phosphate pH 6, 5 mM EDTA, 10 mM β-mercaptoethanol and 0.5% w/v sodium taurocholate) with a mortar and pestle. To recover the IF, the same enzyme extraction buffer was infiltrated into the opposing group of half-leaves by submerging the tissue and applying moderate vacuum pressure. After draining off excess buffer, the undisrupted half-leaves were rolled gently in Parafilm, placed in disposable tubes and the IF collected by low-speed centrifugation. The IF fraction is quite clear and non pigmented and can be applied directly to Phenyl Sepharose hydrophobic resin.
  • The results of a typical experiment are shown in Table 4. The increase in specific activity corresponds to a similar increase in the amount of cross-reacting material observed in a Western blot and is therefore not an artifact of the enzyme assay in the different fractions. Furthermore, rGCB activity was very stable in crude extracts using this particular detergent buffer. The increase in specific activity can therefore be attributed to an enrichment of rGCB in the IF relative to the whole cell homogenate. The actual concentration of rGCB in the IF is likely to be much higher, because PAGE analysis of the IF fraction shows some contamination with known cytoplasmic markers. The highest specific activity we have measured in an IF sample is 20,000 U/mg. If we assume rGCB has the same specific activity as the human enzyme (1.5×10[0170] 6 U/mg), this corresponds to 1.3% of the IF protein obtained by this method.
    TABLE 4
    LOCALIZATION OF rGCB TO THE INTERCELLULAR FLUID
    Fresh Total Protein Total Protein rGCB Total rGCB Specific % Recovery
    Weight Volume Conc. Protein Yield Conc. rGCB Yield Activity rGCB X-Fold
    Sample (gr) (ml) (mg/ml) (mg) (mg/gr) (U/ml) (U) (U/gr) (U/mg) in IF Purification
    Intercellular Fluid 2.48 1.9 0.24  0.45  0.18 720 1368  552 3007 22 18
    Homogenate 2.08 8.1 3.89 31.48 15.13 653 5289 2543  168
  • Specific activity is based on the hydrolysis of 4-MUG inhibited by 0.5 mM CBE. Units (U)=nmol/hr. Because the amount (in nanograms) of cross reacting material observed in a quantitative Western blot corresponds within experimental error to the amount (in nanograms) of enzyme calculated on the basis of activity, we believe the plant rGCB was synthesized with high specific activity. This was a very important and favorable indirect estimate of specific activity. The enzyme was purified to homogeneity to measure more precisely the actual specific activity. [0171]
  • High Levels of rGCB Expression in Leaf Tissue Induce Gene Silencing. The T0 individuals described in Table 4 are by definition hemizygous. They contain various loci generated from independent insertion events, having no corresponding insert on the homologous chromosome. The thirteen T0 individuals from Group A were self-pollinated and assayed for levels of enzyme expression in the T1 generation in order to analyze the effects of gene dosage (homozygotes versus hemizygotes) and to identify candidate T1 families for future seed increase. Kanamycin-resistant transgenic plants were randomly selected from segregating families and analyzed for rGCB expression. The number of probable loci was estimated by chi-square analysis of the linked kanamycin-resistant phenotype at >95% confidence level. There are several T1 families with a heritable mean rGCB activity in the range of 200-300 U/mg (nmol 4-MUG hydrolyzed per hour) in the total homogenates that we have selected for further production of the enzyme (Table 5). [0172]
    TABLE 5
    EXPRESSION OF rGCB IN THE T1 GENERATION
    Mean Specific
    Tobacco T1 Number Activity Standard Number of
    Cultivar Family of Loci Units/mg Error Individuals
    Samsun 963 2 294 25 23
    Samsun 881 1 242 22 16
    MD609 920 1 205 15 38
    Xanthi 902 1 202 17 5
    Samsun 883 1 201 18 13
    Xanthi 832 1 195 18 9
    SR1 826 1 184 16 40
    SR1 834 1 145 9 32
    Xanthi 851 1 140 15 5
    Samsun 837 1 129 16 8
    Xanthi 831 1 114 21 10
    Xanthi 833 1 107 12 5
    Xanthi 807 1 to 2 87 12 9
    Controls 40 8 20
  • However, of 235 T1 plants analyzed, the single individual having the highest activity and the single observation of completely null expression were siblings of the T1 family 826. Moreover, extracts from 826 were also quantitatively the second highest sample of the original 46 analyzed for enzyme activity in the T0 generation. By Western blot, we analyzed protein extracts from several T1 siblings of this family, including the highest (612 U/mg) and the lowest (0 U/mg) and found a clear linear correlation between the amount of cross-reacting protein at 59 kDa and the activity loaded in each lane. In addition to the 59 kDa band, there were also variable amounts of cross-reacting protein at 52 kDa. In the null individual there was only the 52 kDa protein. We never observed this molecular weight species in the T0 extracts or in any other T1 family. There was no evidence of proteolytic activity in this sample as judged by mixing the null sample with high activity extracts and analyzing by enzyme assays and Western blots after incubation at 37° C. If the apparently truncated rGCB was derived from proteolytic cleavage, the protease activity must be both physiologically induced and inactive under these isolation conditions. When the null individual was self-pollinated and the T2 generation analyzed, enzyme expression reappeared as in the T1 and T0. Our working hypothesis was that the tobacco plant is able to limit the expression of the foreign enzyme as constitutively expressed from this cDNA construct, and that the threshold for the stochastic induction of this response during development occurs at an expression level corresponding to approximately 600 U/mg specific activity in the crude homogenate. Of the lines we created, 826 were able to produce enough mRNA to exceed this threshold in the homozygous state. [0173]
  • The silencing of genes in plants is a recently described phenomenon. Work has been done detailing a cellular surveillance mechanism that has apparently evolved to specifically degrade excess RNA (36). In one case, specific RNA cleavages near the 3′-end of the transcript initiate the removal of the transcript. Our description of the silencing of rGCB above 600 U/mg is the first association of silencing with a truncated protein, and may well be caused by a specific mRNA (and not protein) cleavage event. Gene silencing may determine an upper limit of expression attainable using constitutive transgene expression. [0174]
  • We subcloned the cDNA for glucocerebrosidase into a TMV-transient vector and cDNA combinations. Transcripts were synthesized in vitro and inoculated directly onto lower leaves of whole plants. In each case, there was an additional lag time of about 2 weeks post-inoculation before appearance of virus in the upper leaves of the plant and in each case the viral population no longer carried a significant portion of the gene. We detected no significant enzyme activity in either inoculated or systemically infected leaves. Very recently, we detected the gene in root tissue and in transfected protoplasts. There appears to be an incompatibility with leaf expression under conditions of viral amplification of the rGCB mRNA. This incompatibility selects for loss of the sequence from the viral population. [0175]
  • To further investigate the nature of the leaf incompatibility with rGCB expression, we built the construct pBSG641. This plasmid contains the rGCB gene substituted into the coat protein region. The remaining portion of the entire genome was then placed under control of the 35S promoter. The promoter was designed to initiate RNA synthesis such that the correct 5′-end of TMV would be synthesized. A custom-designed, self-cleaving ribozyme sequence positioned at the end of the genome yields a native 3′-end upon cleavage. The vector was designed for synthesis of infectious transcripts in vivo from a chromosomally integrated locus and production of rGCB through viral amplification of subgenomic mRNA in the cytoplasm. The vector alone without the gene for rGCB produces a systemic but capsid-free, “naked-RNA” infection (38). This RNA co-suppression is the subject of issued U.S. Pat. No. 5,922,602 issued Jul. 13, 1999, the disclosure of which is incorporated herein by reference. [0176]
  • We introduced the construct depicted in FIG. 15 into Agrobacterium and transformed tobacco plants as described above. In this case many of the plant leaves displayed necrotic lesions as transfection events randomly occurred during growth and development and expansion of leaves. These lesions never formed on control transformed plant lines containing vector only sequences capable of replication. These lesions were identical in appearance to the types of lesions induced by plant pathogens during a type of disease resistance reaction, termed the hypersensitive response (HR). Therefore, under conditions where we expect to accumulate large quantities of active enzyme, an HR is signaled by some component of the vector infection specific to rGCB. There are very few of these so-called HR “elicitors” characterized in the literature. Possibly the rGCB enzyme itself, or a secondary metabolite resulting from enzymatic activity, or even rGCB RNA, may induce the HR. In any case, we hypothesize that the HR selects for loss of the gene from the viral RNA population. It is important to remember that this is not a simple genetic instability phenomenon. Under conditions where an HR is not induced, we have synthesized many proteins using TMV-based RNA viral vectors to levels of several percent of the total soluble cell protein without loss of the inserted gene even after virion passage. [0177]
  • Expression of rGCB in Transgenic Tobacco is Robust. In several experiments, we inoculated wild type TMV onto rGCB containing transgenic tobacco and found a ˜1.5-2 fold increase in the specific activity of total homogenates. It appears that the viral infection causes an increase in promoter activity, and/or the secretion and accumulation of active enzyme. This was an important result, because it demonstrates that the expression was compatible with a TMV infection, a physiologically severe stress condition. Furthermore, in separate work, we have used chimeric TMV particles as recombinant carriers for the production of small peptides (31). [0178]
  • Conclusions [0179]
  • We used a wide range of gene expression tools to investigate the accumulation of rGCB in mature tobacco plants. Our results suggest attractive yield, quality and cost objectives can be met with further development. We observed two independent phenomena currently limiting the accumulation of enzyme activity in whole plants; gene silencing in one transgenic line, and a plant leaf hypersensitive response to transient vector mediated synthesis. [0180]
  • These current limitations in gene expression only serve to underscore the advantages and utility of agriculture for recombinant protein production. We have generated several transgenic tobacco lines as a reliable source of biomass for the production of high specific activity enzyme. Because the biomass is accumulated under no sterile growth conditions and production is inexpensively scaled to the quantities desired, it becomes feasible to exploit a dilute but enriched source such as the intercellular fluid fraction for industrial process development. This contrast is most clearly summarized in Table 6. [0181]
    TABLE 6
    INITAL STEPS IN THE PURIFICATION OF GLUCOCEREBROSIDASE
    PLACENTA HOMOGENATE TOBACCO HOMOGENATE TOBACCO LEAF IF
    Specific Specific Specific
    Purification Activity Activity Activity Activity Activity Activity
    Procedure Units/kg Units/mg Recovery % Units/kg Units/mg Recovery % Units/kg Units/mg Recovery %
    Detergent 1,510,000      375 100  1,870,000   230 100  877,000  9,967 100
    Extraction
    Concentration/ 707,000  9,330 47 1,540,000 14,400 82
    Figure US20040234516A1-20041125-P00807
    Figure US20040234516A1-20041125-P00807
    Figure US20040234516A1-20041125-P00807
    Delipidation
    Hydrophobic 554,000 147,000 36 1,242,000 82,000 74 535,000 34,547  61
    Chromatography
  • The placental homogenate procedure is adapted from Furbish et al., (10) starting with a 14,000×g sedimented material. In a typical preparation 15-30 kg of fresh placentas were processed. The tobacco homogenate is based on the average of 2 typical 1 kg extractions of the leaf biomass. The IF data is from an average of 5 small scale extraction experiments (2-200 grams fresh weight), and a single chromatography run of an IF concentrate. For comparative purposes all yields are normalized to 1 kg. [0182]
    TABLE 7
    GCB IF PILOT PROCESS
    Greenhouse Scale (1 kg) Field Scale (100 kg)
    Specific Total Specific Total
    Purification Activity Activity Purification Activity Activity Purification
    Step Units/kg Units/mg Recovery % Fold Units/kg Units/mg Recovery % Fold
    IF 4,153,533  20,388 100 1.0 434,927  2,745 100 1.0
    Phenyl SL 3,738,180 147,813 91.4 7.25 194,722 12,960 44.4 5.0
    SP Big 2,740,086 650,377 67.0 31.9 145,060 99,220 33.1 38.2
    Beads
  • For comparative purposes all yields are normalized to 1 kg. The greenhouse/laboratory scale process is based on an average of 2 infiltration/chromatography runs starting with 1 kilogram of fresh weight leaf tissue. [0183]
  • The GenBank accession No. for glucocerebrosidase is M11080. The field scale process is an average of 7 large scale infiltrations consisting of 100 kilograms of fresh weight tissue. Enzyme activity is based on the cleavage of 4-methylumbelliferylglucoside (1 Unit=1 nmol/hr). One factor contributing to a lower apparent yield in the field on a fresh weight basis is that rGCB is concentrated in the leaf lamina and in the lab scale procedure the midrib was removed. [0184]
  • Preparation of Solutions for GCB Assay with 4-Methylumbelliferyl β-D-Glucopyranoside [0185]
  • 1. GCB Assay Buffer [0186]
  • 0.1 M Potassium Phosphate, 0.15% Triton X-100, 0.125% sodium taurocholate (Sigma T-4009), 0.1% bovine serum albumin, 0.02% sodium azide, pH 5.9 [0187]
  • Dissolve 13.6 grams of potassium phosphate monobasic (KH[0188] 2PO4) in 950 ml of distilled water. Add 1.25 g of sodium taurocholate and 1.5 g of Triton X-100. Triton X-100 is a very viscous liquid and should be weighed rather than pipetted in order to achieve a reproducible buffer. Add 2 ml of 10% sodium azide and 1 gram of bovine serum albumin (BSA). Stir until all material has dissolved. Adjust the pH to 5.9 by the addition of a small amount of 1 N NaOH, then bring up to 1000 ml with water.
  • Filter sterilize and store at 4° C. This buffer is stable for many months. [0189]
  • 2. Stopping Buffer [0190]
  • 0.1 M Glycine in 0.1 M NaOH [0191]
  • Dissolve 4 grams of NaOH and 7.51 grams of glycine in 1 liter of distilled water. Filter sterilize and store at 4° C. (Stable for years at 4° C.). [0192]
  • 3. Substrate (Sigma M-3633) FW 338.3 [0193]
  • 15 mM 4-methylumbelliferyl β-D-glucopyranoside (4-MUG) in assay buffer [0194]
  • Weigh out 1 gram of 4-MUG into a 500 ml Erlenmeyer flask. Add exactly 197 ml of Assay Buffer (Substrate dilution Buffer) and heat in a hot water bath to dissolve. Caution: Heating too aggressively results in unacceptably high background fluorescence. [0195]
  • After cooling, dispense into 5-7 ml aliquots in 15 ml polypropylene tubes, let tubes cool to room temperature and freeze at −20° C. for later use. [0196]
  • 4. 125 mM Conduritol β-Epoxide (CBE) (Toronto Research C-66600) [0197]
  • MW=162.18 [0198]
  • Dissolve 100 mg of CBE in 4.92 ml of 0.1 M KPO[0199] 4 Buffer, pH 6.0. Dispense into 200-500 μl aliquots and store at −20° C.
  • 5. 0.1 M KPO[0200] 4 Buffer, pH 6.0
  • 1.75 ml of 0.5 M KH[0201] 2PO4 (Solution A) 87.5 mM
  • 0.246 ml of 0.5 M K[0202] 2HPO4 (Solution B) 12.3 mM
  • Add distilled water to 10 ml. [0203]
  • Reagents: [0204]
    Potassium Phosphate Monobasic (KH2PO4) Fisher Scientific P285
    Potassium Phosphate Dibasic (K2HPO4) Fisher Scientific P288
    Triton X-100 Sigma X-100
    Sodium Taurocholic Acid Sigma T-4009
    Bovine Serum Albumin, Fraction V Sigma A-2153
    Sodium Azide Sigma S-2002
    Glycine Sigma G-4392
    Sodium Hydroxide Pellets Fisher Scientific S318
    Conduritol β-epoxide (CBE) Toronto Research C-66600
    4-Methylumbelliferyl β-D-glucopyranoside MW = 162.18
    (β-D-glucoside) Sigma M-3633
  • GCB Assay with 4-Methylumbelliferyl β-D-Glucopyranoside (MUG) [0205]
  • 1.0 Purpose [0206]
  • To measure the amount of glucocerebrosidase activity from transgenic tobacco plants following infiltration and/or homogenization of the tissue. Measurement of fluorometric activity requires an accurate determination and relationship between fluorescence of the released methylumbelliferone and its concentration under the assay conditions. [0207]
  • Scope [0208]
  • This is an inhibition assay. CBE inhibits human GCB. The fluorescent value used to calculate activity is based on the difference in values with and without inhibitor present. The fluorescent value with CBE (plant glucosidase) is subtracted from the fluorescent value without inhibitor which is both plant and human GCB activity. The difference being the value for human GCB expressed in the transgenic plants. The assay is carried out using 5 μl of sample with 45 μl assay buffer ±CBE at 37° C. This means that 2 tubes are needed per sample. This procedure is applicable to the Glucocerebrosidase assay procedure requiring a methylumbelliferone standard curve. [0209]
  • Equipment [0210]
  • Fluorometer (St. John Associates Fluoro-Tec 2001A with KV-418 filter and 365 nm interference filter) [0211]
  • 10×75 mm cuvettes (St. John Associates) [0212]
  • Water Bath [0213]
  • Test Tubes 13×100 mm glass (VWR or equivalent) [0214]
  • 4-Methylumbelliferone (Sigma M-1381) [0215]
  • Pipettes and pipette tips, 5 μl-1 ml (Rainin or equivalent) [0216]
  • 1.5 ml microfuge tubes [0217]
  • Precautions [0218]
  • The fluorometer should be warmed up for at least 20 minutes prior to reading samples. The power switch should be left on at all times. If the power switch was turned off it may take longer (up to 1 hour) for the instrument to stabilize. [0219]
  • Be certain to put away all reagents under proper storage conditions after reading assays. Any left over fluorescent substrates and CBE stock should be returned to −20° C. The fluorescent substrate and CBE stock can be frozen and thawed numerous times without any breakdown of the reagents. Do not save any substrate or assay buffer to which you added CBE. These should be discarded. You should only make up enough reagent with the inhibitor (CBE) that you currently need. [0220]
  • Procedure [0221]
  • 1. Turn on the water bath and check to be certain the temperature is set to 37° C. [0222]
  • 2. Turn on fluorometer to warm up by flipping up the PMT switch. It should be turned on at least 15-20 minutes before taking readings. If the power switch was turned off it may take longer (up to 1 hour) for the instrument to stabilize. [0223]
  • 3. Remove assay buffer from refrigerator and CBE from −20° C. freezer. Thaw CBE on ice. [0224]
  • 4. Defrost the appropriate amount of methylumbelliferyl β-D-glucopyranoside (MUG) substrate. You need 400 μl of MUG for each sample (±CBE). Place tubes in 37° C. H[0225] 2O bath for approximately 10 minutes to get MUG into solution. Note: There may be a small amount of insoluble material (MUG) in each tube even after the 10 minutes at 37° C. Vortex before use. Keep at room temperature until ready to use.
  • 5. Remove enough GCB Assay Buffer from the stock bottle that will be needed for your samples and transfer to a 15 ml tube. Add appropriate amount of 125 mM stock solution of CBE to assay buffer so the final concentration is 0.55 mM CBE. CBE stock is stored at −20° C. Thaw some CBE on ice now if you have not already done so. The assay buffer +CBE may be kept at room temperature if assays will be completed within 1 hour otherwise store solutions with CBE on ice. [0226]
  • Note: you want the final conc. of CBE in the assay to be 0.5 mM, you are adding 45 μl of buffer to 5 μl of sample so the starting conc. of CBE should be 0.55 mM. [0227]
  • Example: Add 8.8 μl of 125 mM CBE stock solution to 1.991 ml of assay buffer to equal 0.55 mM CBE in assay buffer. This is enough buffer to carry out at least 40 assays. [0228]
  • 6. Label two 13×100 mM glass tubes for each sample to be assayed with a number and the same number and a “+” sign. ( 1, 1+, 2, 2+, etc). Tubes with “+” contain CBE, tubes with just a number will not have CBE added to the assay buffer or MUG. [0229]
  • Carry Out the Following Steps on Ice: [0230]
  • 7. Place numbered tubes in white racks and place in Styrofoam ice chest filled with enough ice and H[0231] 2O (Ice Bath) to cover the volume of fluid in these tubes.
  • 8. Add 45 μl assay buffer to all the tubes with numbers only. [0232]
  • Add 45 μl of assay buffer +CBE to all the “+” tubes. [0233]
  • Place pipette tip in bottom of tube to deliver assay buffer to bottom of tube. [0234]
  • 9. Remove metal tip ejector from P-10 pipetman (so pipetman will reach bottom of tube) and [0235] pipette 5 μl of sample into each set of appropriate tubes of assay buffer (one “+” and one tube with a number only (−CBE) for each sample or twice this number if done in duplicate). Place pipette tip in bottom of tube to deliver sample directly into assay buffer. This is very important since you will be pipetting small volumes into these tubes.
  • Be sure to include a Buffer sample to blank the fluorometer. This will contain 5 μl of the same buffer that the samples are in. [0236]
  • Note: See Dilution of Enzymes if your sample is too concentrated to read in the fluorometer. Basically, dilute your sample 1:5, 1:10, etc. in assay buffer, mix well, pulse in microfuge and add 5 μl of diluted sample to assay buffer above. You should only need 5-10 μl of your sample for the dilutions. [0237]
  • 10. Incubate tubes at 37° C. for 10 minutes then place tubes immediately on ice. [0238]
  • 11. Aliquot the volume of MUG needed for “+” tube assays (200 μl per assay +CBE) into a 15 ml polypropylene tube and add CBE stock to a final concentration of 0.5 mM. [0239]
  • −4 μl of 125 mM CBE per 1 ml MUG in assay buffer=0.5 mM CBE [0240]
  • 12. Add MUG ±CBE to appropriate tubes. [0241]
  • Add 200 μl of MUG without CBE to all the tubes with a number only (−CBE). [0242]
  • Add 200 μl of MUG +CBE to all the “+” tubes. [0243]
  • Place a plastic cap over each tube. Vortex sample and place back on ice. [0244]
  • 13. Transfer all tubes to 37° C. H[0245] 2O bath. Incubate at 37° C. for 15 minutes with shaking. Set the shaker between the # 4-6 settings.
  • 14. Transfer tubes to ice bath. Quickly add 1 ml of stopping solution to each sample. Remove rack of samples from ice. [0246]
  • 15. You are now ready to read samples in fluorometer. [0247]
  • 16. Be certain to put away all reagents under proper storage conditions after reading assays. Any left over fluorescent substrates should be returned to −20° C. The fluorescent substrate and CBE stock can be frozen and thawed numerous times without any breakdown of the reagents. Do not save any substrate or assay buffer to which you added CBE. These should be discarded. You should only make up enough reagent with the inhibitor (CBE) that you currently need. [0248]
  • Dilution of Samples for Assays [0249]
  • Routine dilutions of samples should be carried out on ice using the GCB Assay Buffer described above to maintain enzyme activity. Generally a 1:5 or 1:10 dilution of the sample is sufficient. Dilutions should be carried out in a microfuge tube. ( Example: 1:10 dilution: 5 μl of sample in 45 μl of assay buffer, mix well and pulse sample in microfuge to bring all of the sample to the bottom of the tube). You should only need 5-10 μl of your sample for the dilutions. [0250]
    • EXAMPLE 2
  • Extraction of Glucocerebrosidase Protein [0251]
  • Glucocerebrosidase (GCB), either derived from human placental tissue or a recombinant form from Chinese hamster ovary cells (CHO), is presently used in an effective but costly treatment of the heritable metabolic storage disorder known as Gaucher disease. We combined a dual promoter from Cauliflower Mosaic Virus (35S), a translational enhancer from Tobacco Etch Virus and a polyadenylation region from the nopaline synthetase gene of Agrobacterium tumefaciens with the native human GCB cDNA to create plasmid pBSG638. These expression elements are widely used to provide the highest possible constitutive expression of nuclear encoded genes in plants. The CaMV promoter is further inducible by stress or wound treatment. [0252]
  • Using a standard Agrobacterium-mediated transformation method, we regenerated 93 independent kanamycin-resistant transformants from leaf discs of four different tobacco cultivars (the TO generation). In Western blots of total protein extracts, cross-reacting antigen was detected in 46 of these TO individuals with antibody raised against human glucocerebrosidase. Specificity of the plant-expressed recombinant enzyme was confirmed by hydrolysis of 14C-radiolabeled glucosylceramide. According to these expression results the rGCB positive transformants were ranked into moderate (A), low (B) and negligible (C) activity groups. [0253]
  • We also found reaction conditions to preferentially inhibit rGCB enzyme activity in the presence of plant glucosidases using the suicide substrate conduritol B-epoxide (CBE). Total glucosidase activity, and rGCB activity were measured by hydrolysis of the fluorescent substrate 4-methylumbelliferylglucopyranoside (4-MUG) with and without CBE. Leaves from plants transfected with the vector TT01A 103L were removed at the petiole and slit down the midrib into two equal halves. To obtain a total cellular homogenate, one group of half-leaves was ground in the presence of 4 volumes of detergent extraction buffer (100 mM potassium phosphate p(I 6, 5 mM EDTA, 10 mM, B-mercaptoethanol and 0.5% w/v sodium taurocholate) with a mortar and pestle after freezing the tissue in liquid nitrogen. To recover the intercellular fluid (IF), the same enzyme extraction buffer was infiltrated into the opposing group of half-leaves by submerging the tissue and applying moderate vacuum pressure (500 mm Hg). After draining off excess buffer, the undisrupted half-leaves were rolled gently in Parafilm, placed in disposable tubes and the intercellular fluid (IF) was collected by low-speed centrifugation (1,000 g). The weight of buffer recovered from the infiltrated leaf tissue is recorded and varies from approximately one-half to equal the original weight of the leaf. GCB expression in IF extracts was quantified using a commercially available enzyme assay reagents and protocol. Total protein was determined by the method described by Bradford (Bradford, M. Anal. Biochem 72:248, 1976). [0254]
  • We have demonstrated that active recombinant GCB may be successfully extracted from the intercellular fluid of plant leaves using the present method. The GCB assay is based on MUG hydrolysis in the presence of CBE. The IF method results in a recovery of 22% of the total GCB activity of the leaf at a 18-fold enrichment relative to an extract obtained by homogenization (H). The GCB production results may be improved by optimizing the time post-inoculation with the viral vector and minimizing the contaminating viral coat protein from the intercellular fraction. [0255]
    • EXAMPLE 3
  • Laboratory Pilot Scale Purification of Glucocerebrosidase from the Intercellular Fluid of Tobacco [0256]
  • MD609 leaf tissue (1-2 kilograms) of transgenic tobacco expressing the lysosomal enzyme glucocerebrosidase was harvested, the mid vein removed and the tissue weighed. Tissue was submerged with 2-4 volumes of buffer (0.1 M KPO[0257] 4 buffer, pH 6.0, 5 mM EDTA, 0.5% taurocholic acid, 10 mM β-mercaptoethanol) in an infiltration vessel that accommodates several kilograms of leaf tissue at one time. A perforated metal plate was placed on top of tissue to weigh down the tissue. A vacuum of 25-27 in. Hg was applied for 1-2 minutes×3. The vacuum was released between subsequent applications. Tissue was rotated and the vacuum reapplied to achieve complete infiltration. Multiple applications of the vacuum without isolating the intercellular fluid constitutes a single infiltration procedure. An indication of complete infiltration is a distinct darkening in color of the underside of the leaf tissue. Excess buffer on the tissue was drained. The intercellular fluid was released from the tissue by centrifuging the tissue in a basket rotor at 4200 RPM (2500×g) for 10 minutes. The intercellular fluid was collected using an aspirator hooked up to a vacuum pump (IF-1). Alternatively, the leaf tissue can be re-infiltrated by placing the leaves back in the infiltration vessel in the same buffer used above and the process repeated (IF-2). The second infiltration does not require as many applications of the vacuum. Additionally, the buffer may be drained from the infiltration vessel (spent buffer) and pooled with the 1st and 2nd IF fractions. Collectively, IF-1, IF-2 and Spent Buffer constitutes the IF pool. The volume of intercellular fluid collected from the infiltrated leaf tissue was between 50-100% of the leaf tissue by weight depending on the number of infiltrations carried out.
  • Recombinant GCB was purified by loading the dilute intercellular (feed stream) directly on a [0258] Pharmacia Streamline 25 column containing Phenyl Streamline resin. Expanded bed chromatography enabled us to capture, clarify and concentrate our protein in one step without the need for centrifugation and/or microfiltration steps. The column was equilibrated and washed until UV-signal on recorder returned to baseline with 25 mM citrate, 20% ethylene glycol, pH 5.0 and then eluted with 25 mM citrate, 70% ethylene glycol. The eluted material was further purified on a cation exchange resin, SP Big Beads (Pharmacia), equilibrated in 25 mM citrate, 75 mM NaCl, pH 5.0. GCB was eluted with either a step gradient of 25 mM citrate, 0.5 M NaCl, 10% ethylene glycol, pH 5.0 or a linear gradient of 75 mM-0.4 M NaCl in 25 mM citrate, pH 5.0. All chromatography steps were carried out at room temperature.
  • Using the suicide substrate, conduritol β-epoxide (CBE), inhibition of recombinant glucocerebrosidase (rGCB) activity in the presence of plant glucosidases was achieved. Enzyme activity was measured at 37° C. in a reaction mixture containing 5 mM methylumbelliferyl β-D glucoside, 0.1 M Potassium Phosphate, 0.15% Triton-X100, 0.125% sodium taurocholate, 0.1% bovine serum albumin, pH 5.9 with and without CBE. Total glucosidase activity and rGCB activity were measured by hydrolysis of the fluorescent substrate 4-methylumbelliferyl glucopyranoside. One unit of activity is defined as the amount of enzyme required to catalyze the hydrolysis of 1 nmol of substrate per hour. Total protein was determined using the Bio-Rad Protein Assay based on the method of Bradford (Bradford, M. Anal. Biochem. 72:248; 1976). [0259]
  • Typically from 1 kilogram of leaves where IF-1 alone was collected we obtained 4 million unites of GCB at a specific activity of 20,000. The Units/kg increased to 6 million with a lower specific activity of 10,000 when IF Pool was collected (IF-1, IF-2 and spent buffer). For more information on these experiments, see U.S. Ser. Nos. 09/132,989 and 09/500,554. The disclosures of which are incorporated herein by reference. [0260]
    • EXAMPLE 4
  • Ultrafiltration/Concentration of Intercellular Fluid from Tobacco Expressing Glucocerebrosidase [0261]
  • 2.3 kilograms of MD609 leaf tissue from transgenic tobacco expressing the lysosomal enzyme glucocerebrosidase was harvested, the mid vein removed and the tissue weighed. Tissue was submerged with 2-4 volumes of buffer (0.1 M KPO[0262] 4 buffer, pH 6.0, 5 mM EDTA, 0.5% taurocholic acid, 10 mM β-mercaptoethanol) in an infiltration vessel that accommodates several kilograms of leaf tissue at one time. A perforated metal plate was placed on top of tissue to weigh down the tissue. A vacuum of 25-27 in. Hg was applied for 1-2 minutes×3. The vacuum was released between subsequent applications. Tissue was rotated and the vacuum reapplied to achieve complete infiltration. Excess buffer on the tissue was drained. The intercellular fluid was released from the tissue by centrifuging the tissue in a basket rotor at 4200 RPM (2500×g) for 10 minutes. The intercellular fluid was collected using an aspirator hooked up to a vacuum pump (IF-1). The leaf tissue was re-infiltrated by placing the leaves back in the infiltration vessel in the same buffer used above and the process repeated (IF-2). The buffer was drained from the infiltration vessel (spent buffer) and pooled with the 1st and 2nd IF fractions. Collectively, IF-1, IF-2 and Spent Buffer constitutes the IF pool. The IF pool was filtered through Miracloth and then concentrated 6 fold by passing the IF pool through a 1 sq. ft. spiral membrane (30K molecular weight cutoff) using an Amicon RA 2000 concentrator equipped with an LP-1 pump.
  • Using the suicide substrate, conduritol β-epoxide (CBE), inhibition of recombinant glucocerebrosidase (rGCB) activity in the presence of plant glucosidases was achieved. Enzyme activity was measured at 37° C. in a reaction mixture containing 5 mM methylumbelliferyl β-D glucoside, 0.1 M Potassium Phosphate, 0.15% Triton-X100, 0.125% sodium taurocholate, 0.1% bovine serum albumin, pH 5.9 with and without CBE. Total glucosidase activity and rGCB activity were measured by hydrolysis of the fluorescent substrate 4-methylumbelliferyl glucopyranoside. One unit of activity is defined as the amount of enzyme required to catalyze the hydrolysis of 1 nmol of substrate per hour. Total protein was determined using the Bio-Rad Protein Assay based on the method of Bradford (Bradford, M. Anal. Biochem. 72:248; 1976). [0263]
    • EXAMPLE 5
  • Pilot Scale Purification of Glucocerebrosidase from the Intercellular Fluid of Field Grown Tobacco [0264]
  • 100 kilograms of MD609 leaf tissue from transgenic tobacco expressing the lysosomal enzyme glucocerebrosidase was harvested from the field each day for a period of two weeks. The tissue was stripped off the stalks by hand and weighed. Five kilograms of leaves were placed into polyester bags (Filtra-Spec, 12-2-1053) and four×5 kg bags of leaves were placed into a metal basket. The metal basket containing the leaf material was placed in a 200 L Mueller vacuum tank containing ˜100 liters of buffered solution (0.1 KPO[0265] 4 buffer, pH 6.0, 5 mM EDTA, 0.5% taurocholic acid, 10 mM β-mercaptoethanol). A 70 lb. stainless steel plate was placed over the leaves/bags to assure complete immersion. A vacuum was pulled 27 in. Hg, held for 1 minute and then rapidly released. This vacuum infiltration was repeated for a total of two cycles. Multiple applications of the vacuum without isolating the intercellular fluid constitutes a single infiltration procedure. An indication of complete infiltration is a distinct darkening in color of the underside of the leaf tissue. Following the vacuum infiltrations, the leaves and basket were removed from the vacuum tank. The bags containing the vacuum infiltrated leaves were allowed to gravity drain surface buffer for ˜10 minutes, prior to centrifugation. The intercellular fluid (IF) was recovered from the vacuum infiltrated leaves by centrifugation (1,800×g, 30 minutes) using a Heine basket centrifuge (bowl dimensions, 28.0 inches diameter ×16.5 inches). Collected IF was filtered through a 50 uM cartridge filter and then stored at 4° C., until the entire 100 kilograms of tissue was infiltrated. This process was repeated with the next set of four 5 kg bags (5×20 Kg cycles total) until all the tissue was infiltrated. Additional buffer was added during each infiltration cycle to completely immerse the tissue. Alternatively, the leaf tissue can be re-infiltrated by placing the leaves back in the infiltration vessel in the same buffer used above and the process repeated (IF-2). Additionally, the buffer may be drained from the infiltration vessel (spent buffer) and may be pooled with the 1st and 2nd IF fractions. Collectively, IF-1, IF-2 and Spent Buffer constitutes the IF pool. The volume of intercellular fluid collected from the infiltrated leaf tissue was between 42-170% of the leaf tissue by weight depending on the number of infiltrations carried out.
  • Recombinant GCB was purified by loading the dilute intercellular (feed stream) directly on a [0266] Pharmacia Streamline 200 column containing Phenyl Streamline resin. Expanded bed chromatography enabled us to capture, clarify and concentrate our protein in one step without the need for centrifugation and/or microfiltration steps. The column was equilibrated and washed until UV-signal on recorder returned to baseline with 25 mM citrate, 20% ethylene glycol, pH 5.0 and then eluted with 25 mM citrate, 70% ethylene glycol. The eluted material was sterile filtered by passing the eluted material through a 1 sq. ft. 0.8 um Sartoclean GF capsule followed by a 1 sq. ft. 0.2 um Sartobran P sterile filter (Sartorius, Corp.) and stored at 4° C. until the next chromatography step. The eluted material from 4-5 days of Phenyl Streamline chromatography runs was pooled together and further purified on a cation exchange resin, SP Big Beads (Pharmacia), equilibrated in 25 mM citrate, 75 mM NaCl, pH 5.0. GCB was eluted with a step gradient of 25 mM citrate, 0.4 M NaCl, 10% ethylene glycol, pH 5.0. All chromatography steps were carried out at room temperature. The eluted material was sterile filtered by passing the eluted material through a 1 sq. ft. 0.8 urn Sartoclean GF capsule followed by a 1 sq. ft. 0.2 um Sartobran P sterile filter (Sartorius, Corp.) and stored at 4° C.
  • Using the suicide substrate, conduritol β-epoxide (CBE), inhibition of recombinant glucocerebrosidase (rGCB) activity in the presence of plant glucosidases was achieved. Enzyme activity was measured at 37° C. in a reaction mixture containing 5 mM methylumbelliferyl β-D glucoside, 0.1 M Potassium Phosphate, 0.15% Triton-X100, 0.125% sodium taurocholate, 0.1% bovine serum albumin, pH 5.9 with and without CBE. Total glucosidase activity and rGCB activity were measured by hydrolysis of the fluorescent substrate 4-methylumbelliferyl glucopyranoside. Total protein was determined using the Bio-Rad Protein Assay based on the method of Bradford (Bradford, M. Anal. Biochem. 72:248; 1976). [0267]
  • Typically from 1 kilogram of field grown tobacco, expressing GCB, where IF-1 alone was collected we obtained 435,000 units of GCB at a specific activity of 2,745. The Units/kg increased to 755,000 with a specific activity of 3,400 when IF Pool was collected (IF-1, IF-2 and spent buffer). [0268]
    • EXAMPLE 6
  • Total GCB (IF vs. Homogenate) in “GCB Field Test Virus”[0269]
  • 100 kilograms of MD609 leaf tissue from transgenic tobacco expressing the lysosomal enzyme glucocerebrosidase was harvested from the field each day for a period of two weeks. The tissue was stripped off the stalks by hand and weighed. Five kilograms of leaves were placed into polyester bags (Filtra-Spec, 12-2-1053) and four ×5 kg bags of leaves were placed into a metal basket. The metal basket containing the leaf material was placed in a 200 L Mueller vacuum tank containing ˜100 liters of buffered solution (0.1 KPO[0270] 4 buffer, pH 6.0, 5 mM EDTA, 0.5% taurocholic acid, 10 mM β-mercaptoethanol). A 70 lb. stainless steel plate was placed over the leaves/bags to assure complete immersion. A vacuum was pulled 27 in. Hg, held for 1 minute and then rapidly released. This vacuum infiltration was repeated for a total of two cycles. Following the vacuum infiltrations, the leaves and basket were removed from the vacuum tank. The bags containing the vacuum infiltrated leaves were allowed to gravity drain surface buffer for ˜10 minutes, prior to centrifugation. The intercellular fluid (IF) was recovered from the vacuum infiltrated leaves by centrifugation (1,800×g, 30 minutes) using a Heine basket centrifuge (bowl dimensions, 28.0 inches diameter x 16.5 inches). Collected IF was filtered through a 50 uM cartridge filter and then stored at 4° C, until the entire 100 kilograms of tissue was infiltrated. This process was repeated with the next set of four 5 kg bags (5×20 Kg cycles total) until all the tissue was infiltrated. Additional buffer was added during each infiltration cycle to completely immerse the tissue. In order to evaluate how much enzyme was recovered in the intercellular fluid, the tissue from which the intercellular fluid was isolated was then homogenized in a Waring blender with 4 volumes of the same infiltration buffer as above, centrifuged and the supernatant assayed for enzyme activity.
    • EXAMPLE 7
  • Chops Experiment [0271]
  • An experiment was carried out where 100 kilograms of MD609 leaf tissue of transgenic tobacco expressing the lysosomal enzyme glucocerebrosidase was harvested off the stalks by hand, weighed and chopped into small pieces to increase the surface area for buffer infiltration. Five kilograms of leaves were placed into polyester bags (Filtra-Spec, 12-2-1053) and four ×5 kg bags of leaves were placed into a metal basket. The metal basket containing the leaf material was placed in a 200 L Mueller vacuum tank containing ˜100 liters of buffered solution (0.1 KPO[0272] 4 buffer, pH 6.0, 5 mM EDTA, 0.5% taurocholic acid, 10 mM β-mercaptoethanol). A 70 lb. stainless steel plate was placed over the leaves/bags to assure complete immersion. A vacuum was pulled 27 in. Hg, held for 1 minute and then rapidly released. This vacuum infiltration was repeated for a total of two cycles. Following the vacuum infiltrations, the leaves and basket were removed from the vacuum tank. The bags containing the vacuum infiltrated leaves were allowed to gravity drain surface buffer for ˜10 minutes, prior to centrifugation. The intercellular fluid (IF) was recovered from the vacuum infiltrated leaves by centrifugation (1,800×g, 30 minutes) using a Heine basket centrifuge (bowl dimensions, 28.0 inches diameter ×16.5 inches). Collected IF was filtered through a 50 uM cartridge filter and then stored at 4° C., until the entire 100 kilograms of tissue was infiltrated. This process was repeated with the next set of four 5 kg bags (5×20 Kg cycles total) until all the tissue was infiltrated. Additional buffer was added during each infiltration cycle to completely immerse the tissue. In order to evaluate how much enzyme was recovered in the intercellular fluid, the tissue from which the intercellular fluid was isolated was then homogenized in a Waring blender with 4 volumes of the same infiltration buffer as above, centrifuged and the supernatant assayed for enzyme activity.
  • Recombinant GCB was purified by loading the dilute intercellular (feed stream) directly on a [0273] Pharmacia Streamline 200 column containing Phenyl Streamline resin. The column was equilibrated and washed until UV-signal on recorder returned to baseline with 25 mM citrate, 20% ethylene glycol, pH 5.0 and then eluted with 25 mM citrate, 70% ethylene glycol. All chromatography steps were carried out at room temperature. Table 10 below contains data from the chops experiment.
    • EXAMPLE 8
  • Pilot Scale of Purification of Alpha Galactosidase from the Intercellular Fluid of [0274] Nicotiana benthamiana
  • Young actively growing Nicotiana benthamiana plants were inoculated with infectious transcripts of a recombinant plant viral construct containing the lysosomal enzyme a galactosidase gene. Systemically infected leaf tissue (1-2 kilograms) was harvested from Nicotiana benthamiana expressing a galactosidase 14 days post inoculation. The tissue was weighed and submerged with 2-4 volumes of buffer (25 mM Bis Tris Propane Buffer, pH 6.0, 5 mM EDTA, 0.1 M NaCl, 10 mM β-mercaptoethanol) in an infiltration vessel that can accommodate several kilograms of leaf tissue at one time. A perforated metal plate was placed on top of tissue to weigh down the tissue. A vacuum of 25-27 in. Hg was applied for 30 seconds and then quickly released. The tissue was rotated and the vacuum reapplied to achieve complete infiltration which was confirmed by a distinct darkening in color of the underside of the leaf tissue. Excess buffer on the tissue was drained. The intercellular fluid was released from the tissue by centrifuging the tissue in a basket rotor at 3800 RPM (2100×g) for 10-15 minutes. The intercellular fluid was collected using an aspirator hooked up to a vacuum pump. In some instances only infected leaf tissue was harvested. Alternatively, petioles and stems have been harvested along with the leaf tissue for infiltration. The mid vein was not removed from the tissue prior to infiltration. [0275]
  • Alpha galactosidase was purified by loading the dilute intercellular (fed stream) directly onto a [0276] Pharmacia Streamline 25 column containing Butyl Streamline resin. Expanded bed chromatography enabled us to capture, clarify and concentrate our protein in one step without the need for centrifugation and/or microfiltration steps. The column was equilibrated and washed until UV-signal on recorder returned to baseline with 25 mM Bis Tris Propane, pH 6.0 20% (NH4)2S04 and then eluted with 25 mM Bis Tris Propane, pH 6.0. The eluted material was further purified on Hydroxyapatite equilibrated with 1 mM NaPO4 Buffer, 5% glycerol, pH 6.0 and eluted with either a 1-250 mM NaPO4 buffer, 5% glycerol, pH 6.0 linear gradient or a step gradient. All chromatography steps were carried out at room temperature.
  • Alpha galactosidase activity was measured by hydrolysis of the fluorescent substrate 4-methylumbelliferyl a-D galactopyranoside. Enzyme activity was measured at 37° C. in a reaction mixture containing 5 mM methylumbelliferyl a-D galactopyranoside, 0.1 M Potassium Phosphate, 0.15% Triton-X100, 0.125% sodium taurocholate, 0.1% bovine serum albumin, pH 5.9. Total protein was determined using the Bio-Rad Protein Assay based on the method of Bradford (Bradford, M. Anal. Biochem. 72: 248; 1976). [0277]
  • From 1 kilogram of leaves, we typically obtain between 140-160 million units of α galactosidase at a specific activity of 800,000 following a single infiltration procedure (IF-1). Table 11 below contains data that is representative of several experiments. [0278]
    • EXAMPLE 9
  • Pilot Scale Purification of Glucocerebrosidase from the Intercellular Fluid of Field Grown Tobacco [0279]
  • Transgenic tobacco (MD609) expressing the lysosomal enzyme glucocerebrosidase was mechanically inoculated with a tobacco mosaic virus derivative containing a coat protein loop fusion, TMV291, (Turpen, et.al., 1995, Bio/Technology 13: 23-57). A total of 100 Kg of transgenic, transfected leaf tissue was harvested from the field, five weeks post inoculation. The tissue was stripped off the stalks by hand and weighed. Five kilograms of leaves were placed into polyester bags (Filtra-Spec, 12-2-1053) and four ×5 kg bags of leaves were placed into a metal basket. The metal basket containing the leaf material was placed in a 200 L Mueller vacuum tank containing ˜100 liters of buffered solution (0.1 KPO[0280] 4 buffer, pH 6.0, 5 mM EDTA, 0.5% taurocholic acid, 10 mM β-mercaptoethanol). A 70 lb. stainless steel plate was placed over the leaves/bags to assure complete immersion. A vacuum was pulled 27 in. Hg, held for 1 minute and then rapidly released. This vacuum infiltration was repeated for a total of two cycles. Multiple applications of the vacuum without isolating the intercellular fluid constitutes a single infiltration procedure. An indication of complete infiltration is a distinct darkening in color of the underside of the leaf tissue. Following the vacuum infiltrations, the leaves and basket were removed from the vacuum tank. The bags containing the vacuum infiltrated leaves were allowed to gravity drain surface buffer for ˜10 minutes, prior to centrifugation. The intercellular fluid (IF) was recovered from the vacuum infiltrated leaves by centrifugation (1,800×g, 30 minutes) using a Heine basket centrifuge (bowl dimensions, 28.0 inches diameter ×16.5 inches). Collected IF was filtered through a 50 uM cartridge filter and then stored at 4° C., until the entire 100 kilograms of tissue was infiltrated. This process was repeated with the next set of four 5 kg bags (5×20 Kg cycles total) until all the tissue was infiltrated. Additional buffer was added during each infiltration cycle to completely immerse the tissue.
  • Recombinant GCB was purified by loading the dilute intercellular (feed stream) directly on a [0281] Pharmacia Streamline 200 column containing Phenyl Streamline resin. Expanded bed chromatography enabled us to capture, clarify and concentrate our protein in one step without the need for centrifugation and/or microfiltration steps. The column was equilibrated and washed until UV-signal on recorder returned to baseline with 25 mM citrate, 20% ethylene glycol, pH 5.0 and then eluted with 25 mM citrate, 70% ethylene glycol. The eluted material was sterile filtered by passing the eluted material through a 1 sq. ft. 0.8 um Sartoclean GF capsule followed by a 1 sq. ft. 0.2 urn Sartobran P sterile filter (Sartorius, Corp.) and stored at 4° C. until the next chromatography step. The eluted material from 4-5 days of Phenyl Streamline chromatography runs was pooled together and further purified on a cation exchange resin, SP Big Beads (Pharmacia), equilibrated in 25 mM citrate, 75 mM NaCl, pH 5.0. GCB was eluted with a step gradient of 25 mM citrate, 0.4 M NaCl, 10% ethylene glycol, pH 5.0. All chromatography steps were carried out at room temperature. The eluted material was sterile filtered by passing the eluted material through a 1 sq. ft. 0.8 um Sartoclean GF capsule followed by a 1 sq. ft. 0.2 um Sartobran P sterile filter (Sartorius, Corp.) and stored at 4° C.
  • Using the suicide substrate, conduritol β-epoxide (CBE), inhibition of recombinant glucocerebrosidase (rGCB) activity in the presence of plant glucosidases was achieved. Enzyme activity was measured at 37° C. in a reaction mixture containing 5 mM methylumbelliferyl β-D glucoside, 0.1 M Potassium Phosphate, 0.15% Triton-X100, 0.125% sodium taurocholate, 0.1 % bovine serum albumin, pH 5.9 with and without CBE. Total glucosidase activity and rGCB activity were measured by hydrolysis of the fluorescent substrate 4-methylumbelliferyl glucopyranoside. Total protein was determined using the Bio-Rad Protein Assay based on the method of Bradford (Bradford, M. Anal. Biochem. 72:248; 1976). Table 7 contains the GCB recovery data from TMV transfected plant tissue. [0282]
  • The quantity of virus present in IF extracted leaf tissue was determined using homogenization and polyethylene glycol precipitation methods. In addition, the amount of virus present in the pooled, intercellular fluid was determined by direct polyethylene glycol precipitation. Final virus yields from precipitated samples was determined spectrophotometrically by absorbance at 260 nm. [0283]
    TABLE 8
    Sample Virus Titer
    IF extracted leaf tissue 0.206 mg virus/g fresh weight
    Pooled IF 0.004 mg virus/g fresh weight,
    0.010 mg virus/ml IF
    • EXAMPLE 10
  • Making rGAL-A Enzyme [0284]
  • Experimental Results. Achieving high steady-state mRNA levels is a prerequisite for vector development. However, there are many complex biochemical and host compatibility interactions that ultimately determine the overall performance of a heterologous expression system for a given protein. For this reason, we initiated some preliminary experiments to test the potential for RNA-viral mediated synthesis of active rGal-A in whole plants. [0285]
  • In order to ensure efficient delivery of rGal-A into the lumen of the plant endoplasmic reticulum, we fused the Gal-A cDNA (31) to a plant signal peptide sequence derived from rice α-amylase gene (32,33). We also hypothesized that addition of an ER-retention signal (SEKDEL) (SEQ ID NO:37) might prolong the resident time of the recombinant protein in the ER to increase the fraction of correctly assembled and catalytically active enzyme under extreme conditions of protein synthesis. These constructs were subcloned into the viral vector TTODA, a chimera between tobacco and tomato mosaic viruses (FIG. 1). Transcripts were prepared in vitro and inoculated onto the lower leaves of whole plants (Nicotiana benthamiana). 1-3 weeks after inoculation, leaves were weighed, rolled in a strip of Parafilm and placed in a disposable chromatography column and submerged in enzyme extraction buffer (0.1 M K/P04, 0.1 M NaCl, 5 mM EDTA, 10 mM β-ME and 0.5% sodium taurocholate, pH 6.0). In order to infiltrate the buffer into the tissue, a vacuum of 730-750 mmHg was twice applied. After draining the excess buffer, the intercellular fluid fraction was recovered by low-speed centrifugation (˜1,500×g, 15 min). To measure enzyme remaining in the tissue after this treatment, the leaf was unrolled after centrifugation and two discs removed with a #14 cork borer. This tissue sample was transferred to an eppendorf tube, frozen in liquid nitrogen and ground in four volumes of enzyme extraction buffer. In rGal-A enzyme assays, we measured cleavage of the fluorogenic substrate 4-methyl umbeliferyl α-D-galactopyranoside (4-MUG) against known standards using established protocols (34). Units are nmoles of 4-MUG hydrolyzed per hour at 37° C. [0286]
  • In several initial experiments, plant leaves transfected with all constructs accumulated 1-2% of the total soluble plant protein as cross reacting immunologic material (CRIM) using antisera specific for Gal-A in quantitative Western analyses (data not shown). However, enzyme activity was much lower than expected for this amount of CRIM and furthermore was only 2-4 fold higher than activity due to endogenous plant α-galactosidase isozymes. It also appeared that addition of the ER retention signal allowed highest accumulation of steady state activity and that the IF contained little if any additional activity or CRIM. There are three cellular fates for any glycoprotein synthesized in a plant leaf: secretion to the IF, retention in the ER or sorting to the vacuole (35). We reasoned that because the ER retention signal slightly increased expression, the majority of the enzyme was inactivated later in the secretory pathway. This could most likely occur by aggregation in the trans-golgi network as is reported during over-production of this enzyme in CHO-cells (36), and/or in the plant leaf vacuole. The IF fraction is quite clear and non-pigmented and is suitable for direct chromatography. Using the initial construct (rGal-SEKDEL) (SEQ ID NO: 24) we partially purified small amounts of rGal-A from the IF on hydrophobic, lectin and size exclusion resins. [0287]
  • For several plant proteins vacuolar sorting information is located in a carboxy-terminal propeptide (CTPP; 37,38). During the original cloning and characterization of human Gal-A, Quinn et al., postulated a cathepsin-like potential CTPP cleavage for this enzyme at or near two arginine residues, 26 and 28 AA from the termination codon (39,40). The precise AA sequence at the carboxy terminus has, to our knowledge, never been reported. Because secretion in the plant leaf is through a default pathway we reasoned that deletion of specific sorting information from a postulated CTPP might yield more active enzyme in the IF. Analysis of a second set of constructs containing either 12 or 25 AA truncations, with and without the ER retention signal provided dramatic evidence for the significance of this region (See Table 9). In one construct, rGal 12-SEKDEL, virtually all of the CRIM is now assembled and stored as fully active enzyme and is secreted to the IF in significant quantities. As demonstrated in FIG. 3, rGal-A (˜52 kDa) is now the most abundant plant protein in a crude leaf IF sample. The other predominant band at 17.5 kDa is the viral structural protein which likely contaminates this fraction from broken trichomes of the leaf surface. [0288]
    TABLE 9
    rGal-A Expression (U/Gram Leaf Tissue)
    Residual
    Contract/Sample Intercellular Fluid Homogenate Total
    Experiment
    Uninfected Plant 2,800 7,500 10,300
    rGal-A 5,100 10,900 25,000
    rGal-A 5,400 15,000 20,400
    rGal-A-SEKDEL 6,800 30,300 37,100
    rGal-A-SEKDEL 5,200 34,500 39,700
    Experiment
    Uninfected Plant 2,300 4,800 7,100
    rGal-A 25 4,000 8,900 12,900
    rGal-A 25 2,300 9,000 11,300
    rGal-A 25-SEKDEL 3,200 10,000 13,200
    rGal-A 25-SEKDEL 2,800 8,600 11,400
    rGal-A 12 5,500 11,700 17,200
    rGal-A 12-SEKDEL 109,800 117,700 227,500
    rGal-A 12-SEKDEL 199,000 329,500 528,500
    • EXAMPLE 11
  • α-Galactosidase Expression Vector Development, Construction and Testing [0289]
  • The following example describes the series of α-galactosidase vectors that were constructed and tested for enzyme production. Initially, the human α-galactosidase A cDNA (Sugimoto, Y., Aksentijevich, I., Murray, G. J., Brady, R. O., Pastan, I., and Gottesman, M. M. Retroviral coexpression of a multidrug resistance gene (MDRI) and human α-galactosidase A for gene therapy of Fabry disease. Human Gene Therapy 6:905, 1995.)was fused to a plant signal peptide sequence derived from a rice α-amylase gene (Kumagai, M. H., Shah, M., Terashima, M., Vrkljan, Z., Whitaker, J. R., and Rodriguez, R. L. Expression and secretion of rice α-amylase by [0290] Saccharomyces cerevisiae. Gene 94:209, 1990.). This chimeric gene was subcloned into the TMV based expression vector TTODA resulting in a construct designated rGAL-A, see Table 1. Vector rGAL-A was modified by the addition of the putative ER retention signal SEKDEL, resulting in the vector designated rGAL-AR, see Table 1.
  • A series of C-terminal amino acid deletions were introduced into the α-galactosidase gene. Deletions of 4, 8, 12 or 25 codons from the C-terminus of rGAL-A were generated as well as the addition of the putative ER retention sequence (SEKDEL), see Table 10 and FIG. 12 (sequence of TTODA (rGAL-12R). The deletion vectors were designated as described in Table 10: [0291]
    TABLE 10
    Vector Carboxy-Terminal Modifications
    Designation (Amino Acid Sequence)
    rGAL-A TSRLRSHINPTGTVLLQLENTM (SEQ ID NO: 23)
    QMSLKDLL
    rGAL-AR TSRLRSHINPTGTVLLQLENTM (SEQ ID NO: 24)
    QMSLKDLLSEKDEL
    rGAL-4 TSRLRSHINPTGTVLLQLENTM (SEQ ID NO: 25)
    QMSL
    rGAL-4R TSRLRSHINPTGTVLLQLENTM (SEQ ID NO: 26)
    QMSLSEKDEL
    rGAL-8 TSRLRSHINPTGTVLLQLENTM (SEQ ID NO: 27)
    rGAL-8R TSRLRSHINPTGTVLLQLENTM (SEQ ID NO: 28)
    SEKDEL
    rGAL-12 TSRLRSHINPTGTVLLQL (SEQ ID NO: 29)
    rGAL-12R TSRLRSHINPTGTVLLQLSE (SEQ ID NO: 30)
    KDEL
    rGAL-25 TSRLR (SEQ ID NO: 31)
    rGAL-25R TSRLRSEKDEL (SEQ ID NO: 32)
  • The α-galactosidase gene fragment present in vector rGAL-12R was placed into TMV vector SBS5. In addition, the rice (x-amylase signal peptide present in rGAL-12R was replaced by the native human α-galactosidase signal peptide. The resultant vector designated SBS5-rGAL-12R, see FIG. 13, exhibited genetic stability upon serial passage on [0292] N. benthamiana plants.
  • α-galactosidase was extracted from inoculated plants using interstitial fluid and homogenization methods. Fluids were analyzed for α-galactosidase yield, enzyme activity and cellular partitioning and targeting, see Table 11. In all cases, infectious transcripts were prepared in vitro and inoculated onto the lower leaves of actively growing Nicotiana benthamiana plants. Characteristic viral symptoms, vein clearing and leaf curling, were noted ˜6-8 dpi (days post inoculation). Tissue samples were obtained from infected plants 1-3 weeks after inoculation. Leaves were weighed, rolled in a strip of Parafilm and placed in a disposable chromatography column and submerged in extraction buffer (0.1 M K/P04, 0.1 M NaCl, 5 mM EDTA, 10 mM P-ME and 0.5% sodium taurocholate, pH 6.0). Extraction buffer was infiltrated into the tissue by pumping a vacuum of 730-750 mmHg. The vacuum was applied and released two times. After draining the excess buffer, the interstitial fluid (IF) fraction was recovered by low-speed centrifugation (˜1,500×g, 15 min). To measure enzyme remaining in the tissue after this treatment, the leaf was unrolled after centrifugation and two discs (˜1 mg each) removed with a #14 cork borer. This tissue sample was transferred to an Eppendorf tube, frozen in liquid nitrogen and ground in four volumes of extraction buffer. The total homogenate was then subjected to centrifugation at ˜5,000×g and the supernatant fraction was saved for further analysis. [0293]
  • Extracts from IF and homogenates from post-IF leaf tissue were analyzed for enzymatic activity by the hydrolysis of the fluorescent substrate 4-methyl umbeliferyl α-D-galactopyranoside (4-MUG). Known standards and established protocols (Suzuki, K. Enzymatic diagnosis of sphingolipidoses. Meth. Enzy. 138:727, 1987.) were used to obtain the number of enzymatic units (nmoles of 4-MUG hydrolyzed per hour at 37° C.) per gram fresh weight of tissue harvested. [0294]
    TABLE 11
    Interstitial Homogenate Total Enzyme Ratio of
    Vector Fluid Units/ Units/ Activity Activity IF/
    Designation gram leaf gram leaf Units/gram leaf Homogenate
    Uninfected 3,837 9,404 13,241 0.41
    rGAL-A 6,833 189,971 196,804 0.04
    rGAL-AR 6,829 312,068 318,897 0.02
    rGAL-4 16,088 262,806 278,894 0.06
    rGAL-4R 8,245 357,414 365,659 0.02
    rGAL-8 261,814 524,857 789,671 0.50
    rGAL-8R 10,628 469,956 480,584 0.02
    rGAL-12 2,564 8,743 11,307 0.29
    rGAL-12R 305,803 1,033,921 1,339,724 0.30
    rGAL-25 1,265 6,629 7,894 0.19
    rGAL-25R 2,489 6,394 8,883 0.39
  • Enzyme activity data from IF and homogenates derived from plants expressing α-galactosidase from the vectors in Table 2. indicate that carboxy-terminal deletions (4-12 codons) results in increased α-galactosidase expression. Vector rGAL-12R expressed the highest level of total α-galactosidase and also secreted the highest quantity of active enzyme. [0295]
    • EXAMPLE 12
  • Pilot Scale Purification of α-Galactosidase [0296]
  • Actively growing Nicotiana benthamiana plants, propagated in an uncontrolled horticultural greenhouse, were inoculated with encapsidated transcripts derived from the expression vector, SBS5-rGAL-12R. Tissue was harvested 14-17 days post inoculation. Five kilograms of leaves were placed into polyester bags (Filtra-Spec®, 12-2-1053) and four ×5 kg bags of leaves were placed into a metal basket. The metal basket containing the leaf material was placed in a 200 liter Mueller® vacuum tank containing ˜100 liters of buffered solution (50 mM acetate, 5 mM EDTA, 10 mM 2-mercaptoethanol, pH 5.0). A 70 lb. stainless steel plate was placed over the leaves/bags to assure complete immersion. A vacuum was pumped to 695 mm Hg, held for 1 minute and then rapidly released. This vacuum infiltration was repeated for a total of two cycles. Multiple applications of the vacuum without isolating the interstitial fluid constitutes a single infiltration procedure. An indication of complete infiltration is a distinct darkening in color of the underside of the leaf tissue. Following the vacuum infiltrations, the leaves and basket were removed from the vacuum tank. The bags containing the vacuum infiltrated leaves were allowed to gravity drain surface buffer for ˜10 minutes, prior to centrifugation. The interstitial fluid (IF) was recovered from the vacuum infiltrated leaves by centrifugation (1,800×G, 30 minutes) using a HeineS basket centrifuge (bowl dimensions, 28.0 inches diameter ×16.5 inches). The IF was filtered through a 50 μm cartridge filter to remove plant debris prior to purification. [0297]
  • Ammonium sulfate was added to the IF to 15% saturation, mixed for 10 minutes and loaded onto a [0298] Pharmacia Streamline 200 column containing 4 liters of Butyl Streamline resin equilibrated with 25 mM Imidizole, 15% (NH4)2SO4, pH 6.0 at 1.2 L/min. The column was washed to UV baseline with 25 mM Imidizole, pH 6.0, 15% (NH4)2SO4 and α Gal was eluted with a step gradient of 25 mM Imidizole, pH 6.0. The eluent was filtered through a Sartorius glass fiber →0.8 um cartridge filter and loaded directly onto 3 liters of Blue Sepharose in a Pharmacia BPG 200 column equilibrated with 25 mM Imidizole, pH 6.0. The column was washed to UV baseline with 25 mM Imidizole, pH 6.0 and α gal was eluted with a step gradient of 25 mM Imidizole, 650 mM NaCl, pH 6.0. The eluent was concentrated using a 10 kD MWCO, cellulose acetate, 3 ft2 spiral membrane in an Amicon CH-2 concentrator and then sterile filtered.
  • Further purification was carried out either on Octyl Sepharose FF or Hydroxyapatite. For Octyl Sepharose the column was equilibrated with 25 mM Imidizole, 25% ammonium sulfate, pH 6.0 and eluted using a linear gradient of 25-0% (NH[0299] 4)2SO4 in 25 mM Imidizole, pH 6.0. For Hydroxyapatite purification, the sample was dialyzed overnight against 10 mM KPO4Buffer, pH 7.0 and then loaded on a column was equilibrated with 10 mM KPO4Buffer, pH 7.0. The column was washed with equilibration buffer until the UV reached baseline, followed by a linear gradient of 10-200 mM KPO4Buffer, pH 7.0. The α gal flowed through the column free of the contaminating proteins.
  • Alpha gal activity was measured throughout the process with a fluorescent assay using the synthetic substrate, 4-methylumbelliferyl-α-D-galactopyranoside (MU-α gal). Enzyme activity was measured at 37° C. in a reaction mixture containing 5 mM methylumbelliferyl α-D-galactopyranoside, 0.1 M Potassium Phosphate, 0.15% Triton-X100, 0.125% sodium taurocholate, and 0.1% bovine serum albumin, pH 5.9. One unit of enzymatic activity hydrolyzes 1 nmol of MU-α-gal per hour at 37° C. Total protein was determined using the Bio-Rad Protein Assay based on the method of Bradford (Bradford, M. Anal. Biochem. 72: 248; 1976). Results of α-galactosidase activity (Total units and specific activity) from different enzyme production lots are shown in Table 12. [0300]
    TABLE 12
    Kg Specific Activity
    Lot Biomass Total Units/mg protein
    Number Extracted Units (IF) (Purified)
    981215 44.4 2.9 × 109 5.0 × 106
    991115 100 5.5 × 109 3.6 × 106
    991116 120 6.9 × 109 4.0 × 106
    991117 120 5.9 × 109  3.5 × 106*
    991118 95.6 7.0 × 109  3.5 × 106*
    • EXAMPLE 13
  • Analysis of Purified α-Galactosidase [0301]
  • N-terminal Sequence Analysis [0302]
  • N-terminal sequence analysis of α-galactosidase, purified from plants inoculated with transcripts derived from the vector rGAL-12R, MLDNGLARTPT (see SEQ ID NO: 1), had a 100% sequence homology to 11 amino acids of human placental α-galactosidase with the addition of an N-terminal methionine. In contrast, N-terminal sequence of α-galactosidase, purified from plants inoculated with transcripts derived from the vector SBS5-rGAL-12R, LDNGLARTPT (see SEQ ID NO:2), was as expected from native human enzyme. These data indicates the high degree of fidelity that post-translational modifications are carried out within plant leaf cells and that human signal peptides are processed with equal specificity in plants as in the native mammalian source. [0303]
  • C-Terminal Sequence Analysis [0304]
  • C-Terminal sequence of the rGAL-12R and SBS5-rGAL-12R plant produced enzyme was obtained by Edman degradation using the commercial service of the Mayo Foundation. Three cycles were achieved before the signal was too low to read additional sequence. Expected C-Terminus: LLQLSEKDEL (see SEQ ID NO:30). [0305]
    Cycle Major amino acids
    1st L, E
    2nd D, V, A
    3rd Q, G, T
  • It is important to note that the C-terminal amino acid was found to be heterogeneous, either L or E. The presence of glutamic acid in the first cycle greatly reduced the signal because glutamic acid can form a cyclic structure during the activation step that disables cleavage from the chain and therefore blocks a portion of the sample to further sequencing. This reduced that ability of the software to interpret [0306] cycle 3 and beyond. However, the presence of L, E and D in the first two cycles and the absence of other amino acids present in the analysis in an order resembling the α-galactosidase sequence strongly suggests that a population of the enzyme terminates with a DEL sequence as expected from the sequence of the DNA clone.
  • Molecular Weight Determination [0307]
  • The apparent molecular weight of SBS5-rGAL-12R derived α-galactosidase (˜50 kDa) was quite similar to human α-galactosidase A, purified from human placenta, as judged by both coomassie and silver stained SDS-PAGE. However, the protein purified from plant sources showed less molecular weight variation than the native human protein, indicating less heterogeneity in plant glycosylation or a higher purity plant enzyme preparation. [0308]
  • The molecular mass of several lots of plant derived α-galactosidase were determined by MALDI-TOF mass spectroscopy to be 48,963, 48,913, 49,100 daltons. These weights are consistent with the predicted mass of α-galactosidase, based upon amino acid sequence, allowing for broader peaks due to glycosylation. The calculated molecular weight of SBS5-rGAL-12R derived α-galactosidase is 44,619. The difference in predicted and observed mass would equate to approximately 10.0% carbohydrate. [0309]
  • Glycan Analysis [0310]
  • There are four potential N-glycosylation consensus sequences (N—X-T/S) reported for human α gal A (Matsuura, et. al. Glycobiology 8:329-339, 1998). We have identified four potential sites (108, 161, 184, 377) in our plant expressed α gal. One potential glycosylation site, in our α gal, is not glycosylated (377), as is the case for human α gal A expressed in CHO-cells. [0311]
  • Plants have both high mannose and complex glycans that differ from mammalian complex glycans by the presence of an α1,3 fucose on the proximal GlcNac and a β1,2 xylose on the β-linked mannose of the core. Four potential N-glycosylation sites have been identified for the plant derived α-galactosidase. The predicted amino acid sequence has four possible glycosylation sites (Asn-Xaa-Ser/Thr) at Asn residues (108, 161, 184, 377). The glycosylation site at amino acid 377 was not glycosylated, similar to CHO cell derived α-galactosidase glycosylation. The four possible N-glycosylation sites are all located in β turns within hydrophilic regions of the enzyme. It was estimated the mature human α-galactosidase consists of about 370 amino acids and approx. 15% carbohydrate (Calhoun et al. PNAS 82: 7364-7368, 1985). Matsuura et al (Glycobiology 8:329-339,1998) reports that in CHO-cell produced α gal there are four N-glycosylation sites (139, 193, 215, 407) and 3 of the 4 sites are occupied (407 is not glycosylated). [0312]
  • We have determined that our plant expressed protein is indeed glycosylated because the enzyme will bind to ConA which has a specificity for high mannose structures. Also, the plant derived enzyme was chemically deglycosylated with TFMS (trifluoromethanesulfonic acid). The α-galactosidase appeared to be cleaved as observed by a shift in molecular weight on both a silver stained gel and a Western blot with α gal antibody. Early attempts to cleave rGal-A with PNGaseF to release N-linked carbohydrate have been unsuccessful suggesting the presence of α1,3 fucose on the terminal GlcNac of the carbohydrate side chain. This was verified by glycan analysis work carried out by the Glycobiology Core Group at University of California San Diego Cancer Center. Carbohydrate profiling and compositional analysis was done. NMR experiments confirmed that rGal-A from the plant IF contains an N-linked glycan containing plant-specific carbohydrate linkages of a β1,2 xylose and α1,3 fucose on the trimannosyl core. This N-linked structure has been previously reported to occur in glycoproteins isolated from plant seeds and tissue cultures. Five (5) ug was hydrolyzed with 2M TFA for 4 hours and analyzed by HPAEC-PAD. The total amount of sugar and sugar content was 560 ug and 12%. NMR analysis of the major peak showed a trimannosyl-chitobiose core, with α1,3 linked fucose and a β1,2 linked xylose. [0313]
  • α-galactosidase glycan structures were determined by MALDI-TOF and/or MALDI-MS in collaboration with the Universitaet fuer Bodenkultur, see Table 13. For MALDI, 5 μg of plant derived α-galactosidase was digested with pepsin in a mass ratio of 1:40 in 5% formic acid. After evaporation the peptides were dissolved in ammonium acetate buffer, pH 5.0, boiled and subsequently digested with PNGase A overnight. Since the sample has a mass of 49.000 g/mol, there are 100 pmol of glycoprotein. After evaporation, the peptides were removed by cation exchange chromatography and the glycans are analyzed by MALDI (or pyridylaminated). [0314]
  • The molecular mass of the glycan was determined by MALDI-MS using a ThermoBio Analysis DYNAMO (linear MALDI-TOF MS with delayed extraction) instrument. A small portion of the sample was dried on the sample target and subsequently overlaid with “matrix” (gentisic acid). The samples contained complex type sugar chains with fucose, xylose and varying amounts of terminal GlcNAc. Small fractions were devoid of fucose and therefore amenable to hydrolysis by PNGase F. [0315]
    TABLE 13
    Molecular
    Glycan Weight Lot #980805 Lot #981215
    Structure Daltons % Glycan Structure % Glycan Structure
    MOXF 1050.5 3 —
    MMX 1066.5 2 2
    MMXF 1212.7 22 8
    Man 5 1237.5 — 1.8
    GnMX/MGnX 1269.8 6 0.5
    GnMXF/MGnXF 1416.4 53 16
    GnGnX 1473.3 5 7
    GnGnXF 1619.9 9 55
  • [0316]
    TABLE 14
    Characteristic Plant Derived CHO Cell Secreted
    Number of Core Structures 8 23
    Sialic Acid Absent Present
    Xylose β (1, 2) Linkage Absent
    Fucose α (1, 3) Linkage α (1, 6) Linkage
    % Complex Structures
    % Weight Glycosylated 10-12% 15%
    Specific Activity
  • [0317]
    TABLE 15
    α-Galactosidase Specific Activity
    Source 4-MU Substrate Reference
    Nicotiana benthamiana  5.0 × 106 This Patent Application
    Human, Recombinant
    Human Spleen 1.88 × 106 Bishop and Desnick, 1981,
    J. Biol. Chem. 256 (3):
    1307-1316
    Human Placenta 0.99 × 106 Bishop and Desnick, 1981,
    J. Biol. Chem. 256 (3):
    1307-1316
    Human Plasma  7.4 × 105 Bishop and Sweeley, 1978,
    Biochim. Bioph. Acta, 525:
    399-409
  • This example demonstrates the ability to extract two different products from the same leaf tissue based upon extraction procedures that specifically target products localized in the apoplast and cytosol. [0318]
  • Although the invention has been described with reference to the presently preferred embodiments, it should be understood that various modifications can be made without departing from the spirit of the invention. [0319]
  • All publications, patents, patent applications, and web sites are herein incorporated by reference in their entirety to the same extent as if each individual patent, patent application, or web site was specifically and individually indicated to be incorporated by reference in its entirety. [0320]
  • Literature Cited [0321]
  • 1. Brady, R. O. Fabry Disease, In: Peripheral Neropathym 3rd ed., J. W. Griffin, P. A. Low, and J. F. Poduslo (eds.) W. B. Saunders. pp. 1169, 1993. [0322]
  • 2. Desnick, R. J., Ioannou, Y. A., and Eng, C. M. Alpha-Galactosidase A Deficiency: Fabry Disease, In: The Metabolic Bases of Inherited Diseases, C. R. Scriver, A. L. Beaudet, W. S. Sly, D. Valle (eds.) McGraw-Hill, pp. 2741, 1995. [0323]
  • 3. Brady, R. O. Sphingolipidoses, a Medical Progress Report. N. Engl. J. Med. 275: 312, 1966. [0324]
  • 4. Brady R. O., Pentchev P. G., Gal A. E., Hibbert S. R., and Dekaban A. S. Replacement therapy for inherited enzyme deficiency: Use of purified glucocerebrosidase in Gaucher's disease. N. Engl. J. Med. 291:989, 1974. [0325]
  • 5. Furbish F. S., Blair H. E., Shiloach J., Pentchev P. G., and Brady R. O. Enzyme replacement therapy in Gaucher's disease: Large-scale purification of glucocerebrosidase suitable for human administration. Proc. Natl. Acad. Sci. USA 74: 560, 1977. [0326]
  • 6. Furbish F. S., Steer C. J., Krett N. L., and Barranger, J. A. Uptake and distribution of placental glucocerebrosidase in rat hepatic cells and effects of sequential deglycosylation. Biochim. Biophys. Acta 673: 425, 1981. [0327]
  • 7. Barton, N. W., Furbish, F. S., Murray, G. J., Garfield, M., and Brady, R. O. Therapeutic response to intravenous infusions of glucocerebrosidase in a patient with Gaucher disease. Proc. Natl. Acad. Sci. USA 87: 1913, 1990. [0328]
  • 8. Barton, N. W., Brady, R. O., Dambrosia, J. M., DiBisceglie, A. M., Doppelt, S. H., Hill, S. C., Mankin, H. J., Murray, G. J., Parker, R. I., Argoff, C. E., Grewal, R. P., and Yu, K.-T. Replacement therapy for inherited enzyme deficiency-macrophage-targeted glucocerebrosidase for Gaucher's disease. N. Engl. J. Med. 324: 1464, 1991. [0329]
  • 9. Parker, R. I., Barton, N. W., Read, E. J., and Brady, R. O. Hematologic improvement in a patient with Gaucher's disease on long-term replacement therapy: Evidence for decreased splenic sequestration and improved red blood cell survival. Am. J. Hematol. 38: 130, 1991. [0330]
  • 10. Hill, S. C., Parker, C. C., Brady, R. O., and Barton, N. W. MRI of multiple platyspondyly in Gaucher disease: Response to enzyme replacement therapy. J. Comput. Assist. Tomog. 17: 806, 1993. [0331]
  • 11. Beutler, E., Kay, A., Saven, A., Garver, P., Thurston, D., Dawson, A., and Rosenbloom, B. Enzyme replacement therapy for Gaucher disease. Blood 78:1183, 1991. [0332]
  • 12. Fallet, S., Grace, M. E., Sibille, A., Mendelson, D. S., Shapiro, R. S., Hermann, G., and Grabowski, G. A. Enzyme augmentation in moderate to life-threatening Gaucher disease. Pediatr. Res. 31: 496, 1992. [0333]
  • 13. Mistry, P. K., Davies, S., Corfield, A., Dixon, A. K., and Cox, T. M. Successful treatment of bone marrow failure in Gaucher's disease with low-dose modified glucocerebrosidase. Quart. J. Med. New Series 84: 541, 1992. [0334]
  • 14. Grabowski, G. A., Barton, N. W., Pastores, G., Dambrosia, J. M., Baneijee, T. K., McKee, M. A., Parker, C., Schiffinann, R., Hill, S. C., Brady, R. O. Enzyme therapy in [0335] Type 1 Gaucher disease: Comparative efficacy of mannose-terminated glucocerebrosidase from natural and recombinant sources. Ann. Inter. Med. 122:33, 1995.
  • 15. Hasholt L., Sorensen, S. A. A microtechnique for quantitative mesurements of acid hydrolases in fibroblasts. Its application in diagnosis of Fabry disease and enzyme replacement studies. Clin. Chim. Acta 142:257, 1984. [0336]
  • 16. Mapes, C. A., Anderson, R. L., Sweeley, C. C., Desnick, R. J., Krivit, W. Enzyme replacement in Fabry's disease, an inborn error of metabolism. Science 169:987, 1970. [0337]
  • 17. Brady, R. O., Tallman, J. F., Johnson, W. G., Gal, A. E., Leahy, W. R., Quirk, J. M., Dekaban, A. S. Replacement therapy for inherited enzyme deficiency: Use of purified ceramidetrihexosidease in Fabry's disease. N. Eng. J. Med. 289:9, 1973. [0338]
  • 18. Desnick, R. J., Dean, K. J., Grabowski, G. A., Bishop, D. F., Sweeley, C. C. Enzyme therapy XII: Enzyme therapy in Fabry's disease: Differential enzyme and substrate clearance kinetics of plasma and splenic Alpha-galactosidase isozymes. Proc. Natl. Acad. Sci USA 76:5326, 1979. [0339]
  • 19. Beutler, E. The cost of treating Gaucher disease. Nature Medicine 2:523, 1996. [0340]
  • 20. NIH Technology Assessment Panel on Gaucher Disease. Gaucher Disease: Current issues in diagnosis and treatment. JAMA 275:548, 1995. [0341]
  • 21. Hiatt, A., Cafferkey, R., and Bowdish, K. Production of antibodies in transgenic plants. Nature 342:76, 1989. [0342]
  • 22. Assembly of multimeric proteins in plant cells: Characteristics and uses of plant-derived antibodies, In: Transgenic Plants, Fundamentals and Applications, A. Hiatt, (ed.) Marcel Dekker, Inc. New York, NY. pp. 221, 1992. [0343]
  • 23. Ma, J. K.-C., and Hein, M. B. Plant antibodies for immunotherapy. Plant Physiol. 109:341, 1995. [0344]
  • 25. Sijmons, P. C., Dekker, B. M. M., Schrammeijer, B., Verwoerd, T. C., van den Elzen, P. J. M., and Hoekema, A. Production of correctly processed human serum albumin in transgenic plants. Bio/Technology 8:217, 1990. [0345]
  • 26. Mason, H. S., Lam D. M.-K., and Arntzen, C. J. Expression of hepatitis B surface antigen in transgenic plants. Proc. Natl. Acad. Sci. USA 89:11745, 1992. [0346]
  • 27. Haq, T. A., Mason, H. S., Clements, J. D., and Arntzen, C. J. Oral immunization with a recombinant bacterial antigen produced in transgenic plants. Science 268:714, 1995. [0347]
  • 28. Turpen, T. H., Reinl, S. J., Charoenvit, Y., Hoffinan, S. L., Fallarme, V., and Grill, L. K. Malarial epitopes expressed on the surface of recombinant tobacco mosaic virus. Bio/Technology 13:53, 1995. [0348]
  • 29. Kumagai, M. H., Turpen, T. H., Weinzettl, N., della-Cioppa, G., Turpen, A. M., Donson, J., Hilf, M. E., Grantham, G. L., Dawson, W. O., Chow, T. P., Piatak Jr., M., and Grill, L. K. Rapid, high level expression of biologically active □-trichosanthin in transfected plants by a novel RNA viral vector. Proc. Natl. Acad. Sci. USA 90:427, 1993. [0349]
  • 30. Turpen, T. H., and Dawson, W. O Amplification, movement and expression of genes in plants by viral-based vectors, In: Transgenic Plants, Fundamentals and Applications, A. Hiatt, (ed.) Marcel Dekker, Inc. New York, NY. pp. 195, 1992. [0350]
  • 31. Sugimoto, Y., Aksentijevich, I., Murray, G. J., Brady, R. O., Pastan, I., and Gottesman, M. M. Retroviral coexpression of a multidrug resistance gene (MDRI) and human Alpha-galactosidase A for gene therapy of Fabry disease. Human Gene Therapy 6:905, 1995. [0351]
  • 32. O'Neill, S. D., Kumagai, M. H., Majumdar, A., Huang, N., Sutliff, T. D. and Rodriguez, R. L. The α-amylase genes in Oryza sativa: Characterization of cDNA clones and mRNA expression during seed germination. Mol. Gen. Genet. 221:235, 1990. [0352]
  • 33. Kumagai, M. H., Shah, M., Terashima, M., Vrkljan, Z., Whitaker, J. R., and Rodriguez, R. L. Expression and secretion of rice α-amylase by [0353] Saccharomyces cerevisiae. Gene 94:209, 1990.
  • 34. Suzuki, K. Enzymatic diagnosis of sphingolipidoses. Meth. Enzy. 138:727, 1987. [0354]
  • 35. Chrispeels, M. J. Sorting of proteins in the secretory system. Annu. Rev. Plant Physiol. Plant Mol. Biol. 42:21, 1991. [0355]
  • 36. Ioannou, Y. A., Bishop, D. F., and Desnick, R. J. Overexpression of human Alpha-galactosidase A results in its intracellular aggregation, crystallization in lysosomes, and selective secretion. J. Cell Biol. 119:1137, 1992. [0356]
  • 37. Dombrowski, J. E., and Raikhel, N. V. Protein targeting to the plant vacuole—a historical perspective. Brazilian Journal of Medical and Biological Research 29:413, 1996. [0357]
  • 38. Kermode, A. R. Mechanisms of intracellular protein transport and targeting in plant cells. Crit. Rev. Plant Sci. 15:285, 1996. [0358]
  • 39. Bishop, D. F., Calhoun, D. H., Bernstein, H. S., Hantzopoulos, P., Quinn, M., and Desnick, R. J. Human Alpha-galactosidase A: Nucleotide sequence of a cDNA clone encoding the mature enzyme. Proc. Natl. Acad. Sci. USA 83:4859, 1986. [0359]
  • 40. Quinn, M., Hantzopoulos, P., Fidanza, V. and Calhoun, D. H. A genomic clone containing the promoter for the gene encoding the human lysosomal enzyme, Alpha-galactosidase A. Gene 58:177, 1987. [0360]
  • 41. Coppola, G., Yan, Y., Hantzopoulos, P., Segura, E., Stroh, J. G., and Calhoun, D. H. Characterization of glycosylated and catalytically active recombinant human Alpha-galactosidase A using a baculovirus vector. Gene 144:197. [0361]
  • 42. Miyamura, N., Araki, E., Matsuda, K., Yoshimura, R., Furukawa, N., Tsuruzoe, K., Shirotani, T., Kishikawa, H., Yamaguchi, K., and Shichiri, M. A carboxy-terminal truncation of human Alpha-galactosidase A in a heterozygous female with Fabry disease and modification of the enzymatic activity by the carboxy-terminal domain. J. Clin. Invest. 18009, 1996. [0362]
  • 43. National Research Council. Putting biotechnology to work. Bioprocess engineering. National Academy Press, Washington, D.C. 1992. [0363]
  • 44. Prescribing Information, Ceredase™, (alglucerase injection). Genzyme Corporation, January 1995. [0364]
  • 45. Wilkins, T., Bednarek, S. Y., Raikhel, N. V. Role of propetide glycan in post-translational processing and transport of barley lectin to vacuoles in transgenic tobacco. Plant Cell 2:301, 1990. [0365]
  • 46. Melchers, L. S., Sela-Buurlage, M. B., Vloemans, S. A., Woloshuk, C. P., Van Roekel, J. S. C., Pen, J., Van den Elzen, P. J. M., Cornelissen, B. J. C. Extracellular targeting of the vacuolar tobacco proteins AP24, chitinase and □-1,3-glucanase in transgenic plants. Plant Mol. Biol. 21:583, 1993. [0366]
  • 47. Sato, F., Koiwa, H., Sakai, Y., Kato, N., Yamada, Y. Synthesis and secretion of tobacco neutral PR-5 protein by transgenic tobacco and yeast. Biochem. Biophys. Res. Comm. 211:909, 1995. [0367]
  • 48. Maggio, A., D'Urzo, M. P., Abad, L. R., Takeda, S., Hasegawa, P. M., and Bressan, R. Large quantities of recombinant PR-5 proteins from the extracellular matrix of tobacco: Rapid production of microbial-recalcitrant proteins. Plant Mol. Biol. Rep. 14:249, 1996. [0368]
  • 49. Calhoun, D. H., Bishop, D. F., Bernstein, H. S., Quinn, M., Hantzopoulos, P., Desnick, R. J. Fabry disease: Isolation of a cDNA clone encoding human Alpha-galactosidase A. Proc. Natl. Acad. Sci. USA 82:7364, 1985. [0369]
  • 50. Jenkins, N., Parekh, R. B., James, D. C. Getting the glycosylation right: Implications for the biotechnology industry. Nature Biotech. 14:975, 1996. [0370]
  • 51. Fitchette-Lainé, A-C., Gomord, V., Chekkafi, A., and Faye, L. Distribution of xylosylation and fucosylation in the plant Golgi apparatus. Plant J. 5:673, 1994. [0371]
  • 52. Hein, M. B., Tang, Y., McLeod, D. A., Janda, K. D., Hiatt, A. C. Evaluation of immunoglobulins from plant cells. Biotechnol. Prog. 7:455, 1991. [0372]
  • 53. Garcia-Casado, G. Sanchez-Monge, R., Chrispeels, M. J., Armentia, A., Salcedo, G., and Gomez, L. Role of complex asparagine-linked glycans in the allergenicity of plant glycoproteins. Glycobiol. 6:471, 1996. [0373]
  • 54. Chrispeels, M. J., and Faye, L. The production of recombinant glycoproteins with defined non-immunogenic glycans, In: Transgenic Plants, A production system for industrial and pharmaceutical proteins. M. R. L. Owen and J. Pen, (eds.) John Wiley & Sons Ltd. pp. 99, 1996. [0374]
  • 55. von Schaewen, A., Strum, A., O'Neill, J., Chrispeels, M. J. Isolation of a mutant Arabidopsis plant that lacks N-acetyl glucosaminyl transferase I and is unable to synthesize golgi-modified complex N-linked glycans. Plant Physiol. 102:1109, 1993. [0375]
  • 56. Takasaki, S., Murray, G. J., Furbish, F. S., Brady, R. O., Barranger, J. A., and Kobata, A. Structure of the N-asparagine-linked oligosaccharide units of human placental α-glucocerebrosidase. J. Biol. Chem. 259:10112, 1984. [0376]
  • 57. Murray, G. J., Lectin-specific targeting of lysosomal enzymes to reticuloendothelial cells. Meth. Enzy. 149:25, 1987. [0377]
  • 58. Ohshima, T., Murray, G. J., Nagle, J. W., Quirk, J. M., Kraus, M. H., Barton, N. W., Brady, R. O., and Kulkarni, A. B. Structural organization and expression of the mouse gene encoding Alpha-galactosidase A. Gene 166:277, 1995. [0378]
  • 59. Horsch et al., Science 227 (1985) 1229-1231. [0379]
  • 60. An, G., Watson, B D, Chiang, C C Plant Physiol 81 (1986) 301-305. [0380]
  • 61. Gelvin, S B, Schilperoort, R A (eds.) Plant Molec Biol Manual (1988). [0381]
  • 62. Kint, 1971, Arch. Int. Physiol. Biochem. 79:633-644. [0382]
  • 63. Beutler & Kuhl, 1972, Amer. J. Hum. Genet. 24:237-249. [0383]
  • 64. Romeo, et al., 1972, FEBS Lett. 27:161-166. [0384]
  • 65. Wood & Nadler, 1972, Am. J. Hum. Genet. 24:250-255. [0385]
  • 66. Ho, et al., 1972, Am. J. Hum. Genet. 24:256-266. [0386]
  • 67. Desnick, et al., 1973, J. Lab. Clin. Med. 81:157-171. [0387]
  • 68. Desnick, et al., 1989, in The Metabolic Basis of Inherited Disease, Scriver, C. R., Beaudet, A. L. Sly, W. S. and Valle, D., eds, pp. 1751-1796, McGraw Hill, New York. [0388]
  • 70. Kint, 1971, Arch. Int. Physiol. Biochem. 79:633-644. [0389]
  • 71. Beutler & Kuhl, 1972, J. Biol. Chem. 247: 7195-7200. [0390]
  • 72. Callahan, et al., 1973, Biochem. Med. 7: 424-431. [0391]
  • 73. Dean, et al., 1977, Biochem. Biophys. Res. Comm. 77:1411-1417. [0392]
  • 74. Schram, et al., 1977, Biochim. Biophys. Acta. 482:138-144. [0393]
  • 75. Kusiak, et al., 1978, J. Biol. Chem. 253:184-190. [0394]
  • 76. Dean, et al., 1979, J. Biol. Chem. 254:10001-10005. [0395]
  • 77. Bishop, et al., 1980, in Enzyme Therapy in Genetic Disease:2, Desnick, R. J., ed., pp. 17-32, Alan R. Liss, Inc., New York. [0396]
  • 78. Beutler & Kuhl, 1972, J. Biol. Chem. 247:7195-7200. [0397]
  • 79. Schram, et al., 1977, Biochim. Biophys. Acta. 482:138-144). [0398]
  • 80. Kint, 1971; Arch. Int. Physiol. Biochem. 79: 633-644. [0399]
  • 1 37 1 15 PRT Rice 1 Ser Asn Leu Thr Ala Gly Met Leu Asp Asn Gly Leu Ala Arg Thr 1 5 10 15 2 15 PRT Homo sapiens 2 Asp Ile Pro Gly Ala Arg Ala Leu Asp Asn Gly Leu Ala Arg Thr 1 5 10 15 3 1290 DNA Homo sapiens CDS (1)...(1290) 3 atg cag ctg agg aac cca gaa cta cat ctg ggc tgc gcg ctt gcg ctt 48 Met Gln Leu Arg Asn Pro Glu Leu His Leu Gly Cys Ala Leu Ala Leu 1 5 10 15 cgc ttc ctg gcc ctc gtt tcc tgg gac atc cct ggg gct aga gca ctg 96 Arg Phe Leu Ala Leu Val Ser Trp Asp Ile Pro Gly Ala Arg Ala Leu 20 25 30 gac aat gga ttg gca agg acg cct acc atg ggc tgg ctg cac tgg gag 144 Asp Asn Gly Leu Ala Arg Thr Pro Thr Met Gly Trp Leu His Trp Glu 35 40 45 cgc ttc atg tgc aac ctt gac tgc cag gaa gag cca gat tcc tgc atc 192 Arg Phe Met Cys Asn Leu Asp Cys Gln Glu Glu Pro Asp Ser Cys Ile 50 55 60 agt gag aag ctc ttc atg gag atg gca gag ctc atg gtc tca gaa ggc 240 Ser Glu Lys Leu Phe Met Glu Met Ala Glu Leu Met Val Ser Glu Gly 65 70 75 80 tgg aag gat gca ggt tat gag tac ctc tgc att gat gac tgt tgg atg 288 Trp Lys Asp Ala Gly Tyr Glu Tyr Leu Cys Ile Asp Asp Cys Trp Met 85 90 95 gct ccc caa aga gat tca gaa ggc aga ctt cag gca gac cct cag cgc 336 Ala Pro Gln Arg Asp Ser Glu Gly Arg Leu Gln Ala Asp Pro Gln Arg 100 105 110 ttt cct cat ggg att cgc cag cta gct aat tat gtt cac agc aaa gga 384 Phe Pro His Gly Ile Arg Gln Leu Ala Asn Tyr Val His Ser Lys Gly 115 120 125 ctg aag cta ggg att tat gca gat gtt gga aat aaa acc tgc gca ggc 432 Leu Lys Leu Gly Ile Tyr Ala Asp Val Gly Asn Lys Thr Cys Ala Gly 130 135 140 ttc cct ggg agt ttt gga tac tac gac att gat gcc cag acc ttt gct 480 Phe Pro Gly Ser Phe Gly Tyr Tyr Asp Ile Asp Ala Gln Thr Phe Ala 145 150 155 160 gac tgg gga gta gat ctg cta aaa ttt gat ggt tgt tac tgt gac agt 528 Asp Trp Gly Val Asp Leu Leu Lys Phe Asp Gly Cys Tyr Cys Asp Ser 165 170 175 ttg gaa aat ttg gca gat ggt tat aag cac atg tcc ttg gcc ctg aat 576 Leu Glu Asn Leu Ala Asp Gly Tyr Lys His Met Ser Leu Ala Leu Asn 180 185 190 agg act ggc aga agc att gtg tac tcc tgt gag tgg cct ctt tat atg 624 Arg Thr Gly Arg Ser Ile Val Tyr Ser Cys Glu Trp Pro Leu Tyr Met 195 200 205 tgg ccc ttt caa aag ccc aat tat aca gaa atc cga cag tac tgc aat 672 Trp Pro Phe Gln Lys Pro Asn Tyr Thr Glu Ile Arg Gln Tyr Cys Asn 210 215 220 cac tgg cga aat ttt gct gac att gat gat tcc tgg aaa agt ata aag 720 His Trp Arg Asn Phe Ala Asp Ile Asp Asp Ser Trp Lys Ser Ile Lys 225 230 235 240 agt atc ttg gac tgg aca tct ttt aac cag gag aga att gtt gat gtt 768 Ser Ile Leu Asp Trp Thr Ser Phe Asn Gln Glu Arg Ile Val Asp Val 245 250 255 gct gga cca ggg ggt tgg aat gac cca gat atg tta gtg att ggc aac 816 Ala Gly Pro Gly Gly Trp Asn Asp Pro Asp Met Leu Val Ile Gly Asn 260 265 270 ttt ggc ctc agc tgg aat cag caa gta act cag atg gcc ctc tgg gct 864 Phe Gly Leu Ser Trp Asn Gln Gln Val Thr Gln Met Ala Leu Trp Ala 275 280 285 atc atg gct gct cct tta ttc atg tct aat gac ctc cga cac atc agc 912 Ile Met Ala Ala Pro Leu Phe Met Ser Asn Asp Leu Arg His Ile Ser 290 295 300 cct caa gcc aaa gct ctc ctt cag gat aag gac gta att gcc atc aat 960 Pro Gln Ala Lys Ala Leu Leu Gln Asp Lys Asp Val Ile Ala Ile Asn 305 310 315 320 cag gac ccc ttg ggc aag caa ggg tac cag ctt aga cag gga gac aac 1008 Gln Asp Pro Leu Gly Lys Gln Gly Tyr Gln Leu Arg Gln Gly Asp Asn 325 330 335 ttt gaa gtg tgg gaa cga cct ctc tca ggc tta gcc tgg gct gta gct 1056 Phe Glu Val Trp Glu Arg Pro Leu Ser Gly Leu Ala Trp Ala Val Ala 340 345 350 atg ata aac cgg cag gag att ggt gga cct cgc tct tat acc atc gca 1104 Met Ile Asn Arg Gln Glu Ile Gly Gly Pro Arg Ser Tyr Thr Ile Ala 355 360 365 gtt gct tcc ctg ggt aaa gga gtg gcc tgt aat cct gcc tgc ttc atc 1152 Val Ala Ser Leu Gly Lys Gly Val Ala Cys Asn Pro Ala Cys Phe Ile 370 375 380 aca cag ctc ctc cct gtg aaa agg aag cta ggg ttc tat gaa tgg act 1200 Thr Gln Leu Leu Pro Val Lys Arg Lys Leu Gly Phe Tyr Glu Trp Thr 385 390 395 400 tca agg tta aga agt cac ata aat ccc aca ggc act gtt ttg ctt cag 1248 Ser Arg Leu Arg Ser His Ile Asn Pro Thr Gly Thr Val Leu Leu Gln 405 410 415 cta gaa aac aca atg cag atg tct tta aaa gac tta ctt taa 1290 Leu Glu Asn Thr Met Gln Met Ser Leu Lys Asp Leu Leu * 420 425 4 428 PRT Homo sapiens 4 Gln Leu Arg Asn Pro Glu Leu His Leu Gly Cys Ala Leu Ala Leu Arg 1 5 10 15 Phe Leu Ala Leu Val Ser Trp Asp Ile Pro Gly Ala Arg Ala Leu Asp 20 25 30 Asn Gly Leu Ala Arg Thr Pro Thr Met Gly Trp Leu His Trp Glu Arg 35 40 45 Phe Met Cys Asn Leu Asp Cys Gln Glu Glu Pro Asp Ser Cys Ile Ser 50 55 60 Glu Lys Leu Phe Met Glu Met Ala Glu Leu Met Val Ser Glu Gly Trp 65 70 75 80 Lys Asp Ala Gly Tyr Glu Tyr Leu Cys Ile Asp Asp Cys Trp Met Ala 85 90 95 Pro Gln Arg Asp Ser Glu Gly Arg Leu Gln Ala Asp Pro Gln Arg Phe 100 105 110 Pro His Gly Ile Arg Gln Leu Ala Asn Tyr Val His Ser Lys Gly Leu 115 120 125 Lys Leu Gly Ile Tyr Ala Asp Val Gly Asn Lys Thr Cys Ala Gly Phe 130 135 140 Pro Gly Ser Phe Gly Tyr Tyr Asp Ile Asp Ala Gln Thr Phe Ala Asp 145 150 155 160 Trp Gly Val Asp Leu Leu Lys Phe Asp Gly Cys Tyr Cys Asp Ser Leu 165 170 175 Glu Asn Leu Ala Asp Gly Tyr Lys His Met Ser Leu Ala Leu Asn Arg 180 185 190 Thr Gly Arg Ser Ile Val Tyr Ser Cys Glu Trp Pro Leu Tyr Met Trp 195 200 205 Pro Phe Gln Lys Pro Asn Tyr Thr Glu Ile Arg Gln Tyr Cys Asn His 210 215 220 Trp Arg Asn Phe Ala Asp Ile Asp Asp Ser Trp Lys Ser Ile Lys Ser 225 230 235 240 Ile Leu Asp Trp Thr Ser Phe Asn Gln Glu Arg Ile Val Asp Val Ala 245 250 255 Gly Pro Gly Gly Trp Asn Asp Pro Asp Met Leu Val Ile Gly Asn Phe 260 265 270 Gly Leu Ser Trp Asn Gln Gln Val Thr Gln Met Ala Leu Trp Ala Ile 275 280 285 Met Ala Ala Pro Leu Phe Met Ser Asn Asp Leu Arg His Ile Ser Pro 290 295 300 Gln Ala Lys Ala Leu Leu Gln Asp Lys Asp Val Ile Ala Ile Asn Gln 305 310 315 320 Asp Pro Leu Gly Lys Gln Gly Tyr Gln Leu Arg Gln Gly Asp Asn Phe 325 330 335 Glu Val Trp Glu Arg Pro Leu Ser Gly Leu Ala Trp Ala Val Ala Met 340 345 350 Ile Asn Arg Gln Glu Ile Gly Gly Pro Arg Ser Tyr Thr Ile Ala Val 355 360 365 Ala Ser Leu Gly Lys Gly Val Ala Cys Asn Pro Ala Cys Phe Ile Thr 370 375 380 Gln Leu Leu Pro Val Lys Arg Lys Leu Gly Phe Tyr Glu Trp Thr Ser 385 390 395 400 Arg Leu Arg Ser His Ile Asn Pro Thr Gly Thr Val Leu Leu Gln Leu 405 410 415 Glu Asn Thr Met Gln Met Ser Leu Lys Asp Leu Leu 420 425 5 1308 DNA Homo sapiens CDS (1)...(1308) 5 atg cag ctg agg aac cca gaa cta cat ctg ggc tgc gcg ctt gcg ctt 48 Met Gln Leu Arg Asn Pro Glu Leu His Leu Gly Cys Ala Leu Ala Leu 1 5 10 15 cgc ttc ctg gcc ctc gtt tcc tgg gac atc cct ggg gct aga gca ctg 96 Arg Phe Leu Ala Leu Val Ser Trp Asp Ile Pro Gly Ala Arg Ala Leu 20 25 30 gac aat gga ttg gca agg acg cct acc atg ggc tgg ctg cac tgg gag 144 Asp Asn Gly Leu Ala Arg Thr Pro Thr Met Gly Trp Leu His Trp Glu 35 40 45 cgc ttc atg tgc aac ctt gac tgc cag gaa gag cca gat tcc tgc atc 192 Arg Phe Met Cys Asn Leu Asp Cys Gln Glu Glu Pro Asp Ser Cys Ile 50 55 60 agt gag aag ctc ttc atg gag atg gca gag ctc atg gtc tca gaa ggc 240 Ser Glu Lys Leu Phe Met Glu Met Ala Glu Leu Met Val Ser Glu Gly 65 70 75 80 tgg aag gat gca ggt tat gag tac ctc tgc att gat gac tgt tgg atg 288 Trp Lys Asp Ala Gly Tyr Glu Tyr Leu Cys Ile Asp Asp Cys Trp Met 85 90 95 gct ccc caa aga gat tca gaa ggc aga ctt cag gca gac cct cag cgc 336 Ala Pro Gln Arg Asp Ser Glu Gly Arg Leu Gln Ala Asp Pro Gln Arg 100 105 110 ttt cct cat ggg att cgc cag cta gct aat tat gtt cac agc aaa gga 384 Phe Pro His Gly Ile Arg Gln Leu Ala Asn Tyr Val His Ser Lys Gly 115 120 125 ctg aag cta ggg att tat gca gat gtt gga aat aaa acc tgc gca ggc 432 Leu Lys Leu Gly Ile Tyr Ala Asp Val Gly Asn Lys Thr Cys Ala Gly 130 135 140 ttc cct ggg agt ttt gga tac tac gac att gat gcc cag acc ttt gct 480 Phe Pro Gly Ser Phe Gly Tyr Tyr Asp Ile Asp Ala Gln Thr Phe Ala 145 150 155 160 gac tgg gga gta gat ctg cta aaa ttt gat ggt tgt tac tgt gac agt 528 Asp Trp Gly Val Asp Leu Leu Lys Phe Asp Gly Cys Tyr Cys Asp Ser 165 170 175 ttg gaa aat ttg gca gat ggt tat aag cac atg tcc ttg gcc ctg aat 576 Leu Glu Asn Leu Ala Asp Gly Tyr Lys His Met Ser Leu Ala Leu Asn 180 185 190 agg act ggc aga agc att gtg tac tcc tgt gag tgg cct ctt tat atg 624 Arg Thr Gly Arg Ser Ile Val Tyr Ser Cys Glu Trp Pro Leu Tyr Met 195 200 205 tgg ccc ttt caa aag ccc aat tat aca gaa atc cga cag tac tgc aat 672 Trp Pro Phe Gln Lys Pro Asn Tyr Thr Glu Ile Arg Gln Tyr Cys Asn 210 215 220 cac tgg cga aat ttt gct gac att gat gat tcc tgg aaa agt ata aag 720 His Trp Arg Asn Phe Ala Asp Ile Asp Asp Ser Trp Lys Ser Ile Lys 225 230 235 240 agt atc ttg gac tgg aca tct ttt aac cag gag aga att gtt gat gtt 768 Ser Ile Leu Asp Trp Thr Ser Phe Asn Gln Glu Arg Ile Val Asp Val 245 250 255 gct gga cca ggg ggt tgg aat gac cca gat atg tta gtg att ggc aac 816 Ala Gly Pro Gly Gly Trp Asn Asp Pro Asp Met Leu Val Ile Gly Asn 260 265 270 ttt ggc ctc agc tgg aat cag caa gta act cag atg gcc ctc tgg gct 864 Phe Gly Leu Ser Trp Asn Gln Gln Val Thr Gln Met Ala Leu Trp Ala 275 280 285 atc atg gct gct cct tta ttc atg tct aat gac ctc cga cac atc agc 912 Ile Met Ala Ala Pro Leu Phe Met Ser Asn Asp Leu Arg His Ile Ser 290 295 300 cct caa gcc aaa gct ctc ctt cag gat aag gac gta att gcc atc aat 960 Pro Gln Ala Lys Ala Leu Leu Gln Asp Lys Asp Val Ile Ala Ile Asn 305 310 315 320 cag gac ccc ttg ggc aag caa ggg tac cag ctt aga cag gga gac aac 1008 Gln Asp Pro Leu Gly Lys Gln Gly Tyr Gln Leu Arg Gln Gly Asp Asn 325 330 335 ttt gaa gtg tgg gaa cga cct ctc tca ggc tta gcc tgg gct gta gct 1056 Phe Glu Val Trp Glu Arg Pro Leu Ser Gly Leu Ala Trp Ala Val Ala 340 345 350 atg ata aac cgg cag gag att ggt gga cct cgc tct tat acc atc gca 1104 Met Ile Asn Arg Gln Glu Ile Gly Gly Pro Arg Ser Tyr Thr Ile Ala 355 360 365 gtt gct tcc ctg ggt aaa gga gtg gcc tgt aat cct gcc tgc ttc atc 1152 Val Ala Ser Leu Gly Lys Gly Val Ala Cys Asn Pro Ala Cys Phe Ile 370 375 380 aca cag ctc ctc cct gtg aaa agg aag cta ggg ttc tat gaa tgg act 1200 Thr Gln Leu Leu Pro Val Lys Arg Lys Leu Gly Phe Tyr Glu Trp Thr 385 390 395 400 tca agg tta aga agt cac ata aat ccc aca ggc act gtt ttg ctt cag 1248 Ser Arg Leu Arg Ser His Ile Asn Pro Thr Gly Thr Val Leu Leu Gln 405 410 415 cta gaa aac aca atg cag atg tct tta aaa gac tta ctt tct gaa aag 1296 Leu Glu Asn Thr Met Gln Met Ser Leu Lys Asp Leu Leu Ser Glu Lys 420 425 430 gac gaa tta tga 1308 Asp Glu Leu * 435 6 435 PRT Homo sapiens 6 Met Gln Leu Arg Asn Pro Glu Leu His Leu Gly Cys Ala Leu Ala Leu 1 5 10 15 Arg Phe Leu Ala Leu Val Ser Trp Asp Ile Pro Gly Ala Arg Ala Leu 20 25 30 Asp Asn Gly Leu Ala Arg Thr Pro Thr Met Gly Trp Leu His Trp Glu 35 40 45 Arg Phe Met Cys Asn Leu Asp Cys Gln Glu Glu Pro Asp Ser Cys Ile 50 55 60 Ser Glu Lys Leu Phe Met Glu Met Ala Glu Leu Met Val Ser Glu Gly 65 70 75 80 Trp Lys Asp Ala Gly Tyr Glu Tyr Leu Cys Ile Asp Asp Cys Trp Met 85 90 95 Ala Pro Gln Arg Asp Ser Glu Gly Arg Leu Gln Ala Asp Pro Gln Arg 100 105 110 Phe Pro His Gly Ile Arg Gln Leu Ala Asn Tyr Val His Ser Lys Gly 115 120 125 Leu Lys Leu Gly Ile Tyr Ala Asp Val Gly Asn Lys Thr Cys Ala Gly 130 135 140 Phe Pro Gly Ser Phe Gly Tyr Tyr Asp Ile Asp Ala Gln Thr Phe Ala 145 150 155 160 Asp Trp Gly Val Asp Leu Leu Lys Phe Asp Gly Cys Tyr Cys Asp Ser 165 170 175 Leu Glu Asn Leu Ala Asp Gly Tyr Lys His Met Ser Leu Ala Leu Asn 180 185 190 Arg Thr Gly Arg Ser Ile Val Tyr Ser Cys Glu Trp Pro Leu Tyr Met 195 200 205 Trp Pro Phe Gln Lys Pro Asn Tyr Thr Glu Ile Arg Gln Tyr Cys Asn 210 215 220 His Trp Arg Asn Phe Ala Asp Ile Asp Asp Ser Trp Lys Ser Ile Lys 225 230 235 240 Ser Ile Leu Asp Trp Thr Ser Phe Asn Gln Glu Arg Ile Val Asp Val 245 250 255 Ala Gly Pro Gly Gly Trp Asn Asp Pro Asp Met Leu Val Ile Gly Asn 260 265 270 Phe Gly Leu Ser Trp Asn Gln Gln Val Thr Gln Met Ala Leu Trp Ala 275 280 285 Ile Met Ala Ala Pro Leu Phe Met Ser Asn Asp Leu Arg His Ile Ser 290 295 300 Pro Gln Ala Lys Ala Leu Leu Gln Asp Lys Asp Val Ile Ala Ile Asn 305 310 315 320 Gln Asp Pro Leu Gly Lys Gln Gly Tyr Gln Leu Arg Gln Gly Asp Asn 325 330 335 Phe Glu Val Trp Glu Arg Pro Leu Ser Gly Leu Ala Trp Ala Val Ala 340 345 350 Met Ile Asn Arg Gln Glu Ile Gly Gly Pro Arg Ser Tyr Thr Ile Ala 355 360 365 Val Ala Ser Leu Gly Lys Gly Val Ala Cys Asn Pro Ala Cys Phe Ile 370 375 380 Thr Gln Leu Leu Pro Val Lys Arg Lys Leu Gly Phe Tyr Glu Trp Thr 385 390 395 400 Ser Arg Leu Arg Ser His Ile Asn Pro Thr Gly Thr Val Leu Leu Gln 405 410 415 Leu Glu Asn Thr Met Gln Met Ser Leu Lys Asp Leu Leu Ser Glu Lys 420 425 430 Asp Glu Leu 435 7 1278 DNA Homo sapiens CDS (1)...(1275) 7 atg cag ctg agg aac cca gaa cta cat ctg ggc tgc gcg ctt gcg ctt 48 Met Gln Leu Arg Asn Pro Glu Leu His Leu Gly Cys Ala Leu Ala Leu 1 5 10 15 cgc ttc ctg gcc ctc gtt tcc tgg gac atc cct ggg gct aga gca ctg 96 Arg Phe Leu Ala Leu Val Ser Trp Asp Ile Pro Gly Ala Arg Ala Leu 20 25 30 gac aat gga ttg gca agg acg cct acc atg ggc tgg ctg cac tgg gag 144 Asp Asn Gly Leu Ala Arg Thr Pro Thr Met Gly Trp Leu His Trp Glu 35 40 45 cgc ttc atg tgc aac ctt gac tgc cag gaa gag cca gat tcc tgc atc 192 Arg Phe Met Cys Asn Leu Asp Cys Gln Glu Glu Pro Asp Ser Cys Ile 50 55 60 agt gag aag ctc ttc atg gag atg gca gag ctc atg gtc tca gaa ggc 240 Ser Glu Lys Leu Phe Met Glu Met Ala Glu Leu Met Val Ser Glu Gly 65 70 75 80 tgg aag gat gca ggt tat gag tac ctc tgc att gat gac tgt tgg atg 288 Trp Lys Asp Ala Gly Tyr Glu Tyr Leu Cys Ile Asp Asp Cys Trp Met 85 90 95 gct ccc caa aga gat tca gaa ggc aga ctt cag gca gac cct cag cgc 336 Ala Pro Gln Arg Asp Ser Glu Gly Arg Leu Gln Ala Asp Pro Gln Arg 100 105 110 ttt cct cat ggg att cgc cag cta gct aat tat gtt cac agc aaa gga 384 Phe Pro His Gly Ile Arg Gln Leu Ala Asn Tyr Val His Ser Lys Gly 115 120 125 ctg aag cta ggg att tat gca gat gtt gga aat aaa acc tgc gca ggc 432 Leu Lys Leu Gly Ile Tyr Ala Asp Val Gly Asn Lys Thr Cys Ala Gly 130 135 140 ttc cct ggg agt ttt gga tac tac gac att gat gcc cag acc ttt gct 480 Phe Pro Gly Ser Phe Gly Tyr Tyr Asp Ile Asp Ala Gln Thr Phe Ala 145 150 155 160 gac tgg gga gta gat ctg cta aaa ttt gat ggt tgt tac tgt gac agt 528 Asp Trp Gly Val Asp Leu Leu Lys Phe Asp Gly Cys Tyr Cys Asp Ser 165 170 175 ttg gaa aat ttg gca gat ggt tat aag cac atg tcc ttg gcc ctg aat 576 Leu Glu Asn Leu Ala Asp Gly Tyr Lys His Met Ser Leu Ala Leu Asn 180 185 190 agg act ggc aga agc att gtg tac tcc tgt gag tgg cct ctt tat atg 624 Arg Thr Gly Arg Ser Ile Val Tyr Ser Cys Glu Trp Pro Leu Tyr Met 195 200 205 tgg ccc ttt caa aag ccc aat tat aca gaa atc cga cag tac tgc aat 672 Trp Pro Phe Gln Lys Pro Asn Tyr Thr Glu Ile Arg Gln Tyr Cys Asn 210 215 220 cac tgg cga aat ttt gct gac att gat gat tcc tgg aaa agt ata aag 720 His Trp Arg Asn Phe Ala Asp Ile Asp Asp Ser Trp Lys Ser Ile Lys 225 230 235 240 agt atc ttg gac tgg aca tct ttt aac cag gag aga att gtt gat gtt 768 Ser Ile Leu Asp Trp Thr Ser Phe Asn Gln Glu Arg Ile Val Asp Val 245 250 255 gct gga cca ggg ggt tgg aat gac cca gat atg tta gtg att ggc aac 816 Ala Gly Pro Gly Gly Trp Asn Asp Pro Asp Met Leu Val Ile Gly Asn 260 265 270 ttt ggc ctc agc tgg aat cag caa gta act cag atg gcc ctc tgg gct 864 Phe Gly Leu Ser Trp Asn Gln Gln Val Thr Gln Met Ala Leu Trp Ala 275 280 285 atc atg gct gct cct tta ttc atg tct aat gac ctc cga cac atc agc 912 Ile Met Ala Ala Pro Leu Phe Met Ser Asn Asp Leu Arg His Ile Ser 290 295 300 cct caa gcc aaa gct ctc ctt cag gat aag gac gta att gcc atc aat 960 Pro Gln Ala Lys Ala Leu Leu Gln Asp Lys Asp Val Ile Ala Ile Asn 305 310 315 320 cag gac ccc ttg ggc aag caa ggg tac cag ctt aga cag gga gac aac 1008 Gln Asp Pro Leu Gly Lys Gln Gly Tyr Gln Leu Arg Gln Gly Asp Asn 325 330 335 ttt gaa gtg tgg gaa cga cct ctc tca ggc tta gcc tgg gct gta gct 1056 Phe Glu Val Trp Glu Arg Pro Leu Ser Gly Leu Ala Trp Ala Val Ala 340 345 350 atg ata aac cgg cag gag att ggt gga cct cgc tct tat acc atc gca 1104 Met Ile Asn Arg Gln Glu Ile Gly Gly Pro Arg Ser Tyr Thr Ile Ala 355 360 365 gtt gct tcc ctg ggt aaa gga gtg gcc tgt aat cct gcc tgc ttc atc 1152 Val Ala Ser Leu Gly Lys Gly Val Ala Cys Asn Pro Ala Cys Phe Ile 370 375 380 aca cag ctc ctc cct gtg aaa agg aag cta ggg ttc tat gaa tgg act 1200 Thr Gln Leu Leu Pro Val Lys Arg Lys Leu Gly Phe Tyr Glu Trp Thr 385 390 395 400 tca agg tta aga agt cac ata aat ccc aca ggc act gtt ttg ctt cag 1248 Ser Arg Leu Arg Ser His Ile Asn Pro Thr Gly Thr Val Leu Leu Gln 405 410 415 cta gaa aac aca atg cag atg tct tta tga 1278 Leu Glu Asn Thr Met Gln Met Ser Leu 420 425 8 424 PRT Homo sapiens 8 Gln Leu Arg Asn Pro Glu Leu His Leu Gly Cys Ala Leu Ala Leu Arg 1 5 10 15 Phe Leu Ala Leu Val Ser Trp Asp Ile Pro Gly Ala Arg Ala Leu Asp 20 25 30 Asn Gly Leu Ala Arg Thr Pro Thr Met Gly Trp Leu His Trp Glu Arg 35 40 45 Phe Met Cys Asn Leu Asp Cys Gln Glu Glu Pro Asp Ser Cys Ile Ser 50 55 60 Glu Lys Leu Phe Met Glu Met Ala Glu Leu Met Val Ser Glu Gly Trp 65 70 75 80 Lys Asp Ala Gly Tyr Glu Tyr Leu Cys Ile Asp Asp Cys Trp Met Ala 85 90 95 Pro Gln Arg Asp Ser Glu Gly Arg Leu Gln Ala Asp Pro Gln Arg Phe 100 105 110 Pro His Gly Ile Arg Gln Leu Ala Asn Tyr Val His Ser Lys Gly Leu 115 120 125 Lys Leu Gly Ile Tyr Ala Asp Val Gly Asn Lys Thr Cys Ala Gly Phe 130 135 140 Pro Gly Ser Phe Gly Tyr Tyr Asp Ile Asp Ala Gln Thr Phe Ala Asp 145 150 155 160 Trp Gly Val Asp Leu Leu Lys Phe Asp Gly Cys Tyr Cys Asp Ser Leu 165 170 175 Glu Asn Leu Ala Asp Gly Tyr Lys His Met Ser Leu Ala Leu Asn Arg 180 185 190 Thr Gly Arg Ser Ile Val Tyr Ser Cys Glu Trp Pro Leu Tyr Met Trp 195 200 205 Pro Phe Gln Lys Pro Asn Tyr Thr Glu Ile Arg Gln Tyr Cys Asn His 210 215 220 Trp Arg Asn Phe Ala Asp Ile Asp Asp Ser Trp Lys Ser Ile Lys Ser 225 230 235 240 Ile Leu Asp Trp Thr Ser Phe Asn Gln Glu Arg Ile Val Asp Val Ala 245 250 255 Gly Pro Gly Gly Trp Asn Asp Pro Asp Met Leu Val Ile Gly Asn Phe 260 265 270 Gly Leu Ser Trp Asn Gln Gln Val Thr Gln Met Ala Leu Trp Ala Ile 275 280 285 Met Ala Ala Pro Leu Phe Met Ser Asn Asp Leu Arg His Ile Ser Pro 290 295 300 Gln Ala Lys Ala Leu Leu Gln Asp Lys Asp Val Ile Ala Ile Asn Gln 305 310 315 320 Asp Pro Leu Gly Lys Gln Gly Tyr Gln Leu Arg Gln Gly Asp Asn Phe 325 330 335 Glu Val Trp Glu Arg Pro Leu Ser Gly Leu Ala Trp Ala Val Ala Met 340 345 350 Ile Asn Arg Gln Glu Ile Gly Gly Pro Arg Ser Tyr Thr Ile Ala Val 355 360 365 Ala Ser Leu Gly Lys Gly Val Ala Cys Asn Pro Ala Cys Phe Ile Thr 370 375 380 Gln Leu Leu Pro Val Lys Arg Lys Leu Gly Phe Tyr Glu Trp Thr Ser 385 390 395 400 Arg Leu Arg Ser His Ile Asn Pro Thr Gly Thr Val Leu Leu Gln Leu 405 410 415 Glu Asn Thr Met Gln Met Ser Leu 420 9 1296 DNA Homo sapiens CDS (1)...(1296) 9 atg cag ctg agg aac cca gaa cta cat ctg ggc tgc gcg ctt gcg ctt 48 Met Gln Leu Arg Asn Pro Glu Leu His Leu Gly Cys Ala Leu Ala Leu 1 5 10 15 cgc ttc ctg gcc ctc gtt tcc tgg gac atc cct ggg gct aga gca ctg 96 Arg Phe Leu Ala Leu Val Ser Trp Asp Ile Pro Gly Ala Arg Ala Leu 20 25 30 gac aat gga ttg gca agg acg cct acc atg ggc tgg ctg cac tgg gag 144 Asp Asn Gly Leu Ala Arg Thr Pro Thr Met Gly Trp Leu His Trp Glu 35 40 45 cgc ttc atg tgc aac ctt gac tgc cag gaa gag cca gat tcc tgc atc 192 Arg Phe Met Cys Asn Leu Asp Cys Gln Glu Glu Pro Asp Ser Cys Ile 50 55 60 agt gag aag ctc ttc atg gag atg gca gag ctc atg gtc tca gaa ggc 240 Ser Glu Lys Leu Phe Met Glu Met Ala Glu Leu Met Val Ser Glu Gly 65 70 75 80 tgg aag gat gca ggt tat gag tac ctc tgc att gat gac tgt tgg atg 288 Trp Lys Asp Ala Gly Tyr Glu Tyr Leu Cys Ile Asp Asp Cys Trp Met 85 90 95 gct ccc caa aga gat tca gaa ggc aga ctt cag gca gac cct cag cgc 336 Ala Pro Gln Arg Asp Ser Glu Gly Arg Leu Gln Ala Asp Pro Gln Arg 100 105 110 ttt cct cat ggg att cgc cag cta gct aat tat gtt cac agc aaa gga 384 Phe Pro His Gly Ile Arg Gln Leu Ala Asn Tyr Val His Ser Lys Gly 115 120 125 ctg aag cta ggg att tat gca gat gtt gga aat aaa acc tgc gca ggc 432 Leu Lys Leu Gly Ile Tyr Ala Asp Val Gly Asn Lys Thr Cys Ala Gly 130 135 140 ttc cct ggg agt ttt gga tac tac gac att gat gcc cag acc ttt gct 480 Phe Pro Gly Ser Phe Gly Tyr Tyr Asp Ile Asp Ala Gln Thr Phe Ala 145 150 155 160 gac tgg gga gta gat ctg cta aaa ttt gat ggt tgt tac tgt gac agt 528 Asp Trp Gly Val Asp Leu Leu Lys Phe Asp Gly Cys Tyr Cys Asp Ser 165 170 175 ttg gaa aat ttg gca gat ggt tat aag cac atg tcc ttg gcc ctg aat 576 Leu Glu Asn Leu Ala Asp Gly Tyr Lys His Met Ser Leu Ala Leu Asn 180 185 190 agg act ggc aga agc att gtg tac tcc tgt gag tgg cct ctt tat atg 624 Arg Thr Gly Arg Ser Ile Val Tyr Ser Cys Glu Trp Pro Leu Tyr Met 195 200 205 tgg ccc ttt caa aag ccc aat tat aca gaa atc cga cag tac tgc aat 672 Trp Pro Phe Gln Lys Pro Asn Tyr Thr Glu Ile Arg Gln Tyr Cys Asn 210 215 220 cac tgg cga aat ttt gct gac att gat gat tcc tgg aaa agt ata aag 720 His Trp Arg Asn Phe Ala Asp Ile Asp Asp Ser Trp Lys Ser Ile Lys 225 230 235 240 agt atc ttg gac tgg aca tct ttt aac cag gag aga att gtt gat gtt 768 Ser Ile Leu Asp Trp Thr Ser Phe Asn Gln Glu Arg Ile Val Asp Val 245 250 255 gct gga cca ggg ggt tgg aat gac cca gat atg tta gtg att ggc aac 816 Ala Gly Pro Gly Gly Trp Asn Asp Pro Asp Met Leu Val Ile Gly Asn 260 265 270 ttt ggc ctc agc tgg aat cag caa gta act cag atg gcc ctc tgg gct 864 Phe Gly Leu Ser Trp Asn Gln Gln Val Thr Gln Met Ala Leu Trp Ala 275 280 285 atc atg gct gct cct tta ttc atg tct aat gac ctc cga cac atc agc 912 Ile Met Ala Ala Pro Leu Phe Met Ser Asn Asp Leu Arg His Ile Ser 290 295 300 cct caa gcc aaa gct ctc ctt cag gat aag gac gta att gcc atc aat 960 Pro Gln Ala Lys Ala Leu Leu Gln Asp Lys Asp Val Ile Ala Ile Asn 305 310 315 320 cag gac ccc ttg ggc aag caa ggg tac cag ctt aga cag gga gac aac 1008 Gln Asp Pro Leu Gly Lys Gln Gly Tyr Gln Leu Arg Gln Gly Asp Asn 325 330 335 ttt gaa gtg tgg gaa cga cct ctc tca ggc tta gcc tgg gct gta gct 1056 Phe Glu Val Trp Glu Arg Pro Leu Ser Gly Leu Ala Trp Ala Val Ala 340 345 350 atg ata aac cgg cag gag att ggt gga cct cgc tct tat acc atc gca 1104 Met Ile Asn Arg Gln Glu Ile Gly Gly Pro Arg Ser Tyr Thr Ile Ala 355 360 365 gtt gct tcc ctg ggt aaa gga gtg gcc tgt aat cct gcc tgc ttc atc 1152 Val Ala Ser Leu Gly Lys Gly Val Ala Cys Asn Pro Ala Cys Phe Ile 370 375 380 aca cag ctc ctc cct gtg aaa agg aag cta ggg ttc tat gaa tgg act 1200 Thr Gln Leu Leu Pro Val Lys Arg Lys Leu Gly Phe Tyr Glu Trp Thr 385 390 395 400 tca agg tta aga agt cac ata aat ccc aca ggc act gtt ttg ctt cag 1248 Ser Arg Leu Arg Ser His Ile Asn Pro Thr Gly Thr Val Leu Leu Gln 405 410 415 cta gaa aac aca atg cag atg tct tta tct gaa aag gac gaa tta tga 1296 Leu Glu Asn Thr Met Gln Met Ser Leu Ser Glu Lys Asp Glu Leu * 420 425 430 10 431 PRT Homo sapiens 10 Met Gln Leu Arg Asn Pro Glu Leu His Leu Gly Cys Ala Leu Ala Leu 1 5 10 15 Arg Phe Leu Ala Leu Val Ser Trp Asp Ile Pro Gly Ala Arg Ala Leu 20 25 30 Asp Asn Gly Leu Ala Arg Thr Pro Thr Met Gly Trp Leu His Trp Glu 35 40 45 Arg Phe Met Cys Asn Leu Asp Cys Gln Glu Glu Pro Asp Ser Cys Ile 50 55 60 Ser Glu Lys Leu Phe Met Glu Met Ala Glu Leu Met Val Ser Glu Gly 65 70 75 80 Trp Lys Asp Ala Gly Tyr Glu Tyr Leu Cys Ile Asp Asp Cys Trp Met 85 90 95 Ala Pro Gln Arg Asp Ser Glu Gly Arg Leu Gln Ala Asp Pro Gln Arg 100 105 110 Phe Pro His Gly Ile Arg Gln Leu Ala Asn Tyr Val His Ser Lys Gly 115 120 125 Leu Lys Leu Gly Ile Tyr Ala Asp Val Gly Asn Lys Thr Cys Ala Gly 130 135 140 Phe Pro Gly Ser Phe Gly Tyr Tyr Asp Ile Asp Ala Gln Thr Phe Ala 145 150 155 160 Asp Trp Gly Val Asp Leu Leu Lys Phe Asp Gly Cys Tyr Cys Asp Ser 165 170 175 Leu Glu Asn Leu Ala Asp Gly Tyr Lys His Met Ser Leu Ala Leu Asn 180 185 190 Arg Thr Gly Arg Ser Ile Val Tyr Ser Cys Glu Trp Pro Leu Tyr Met 195 200 205 Trp Pro Phe Gln Lys Pro Asn Tyr Thr Glu Ile Arg Gln Tyr Cys Asn 210 215 220 His Trp Arg Asn Phe Ala Asp Ile Asp Asp Ser Trp Lys Ser Ile Lys 225 230 235 240 Ser Ile Leu Asp Trp Thr Ser Phe Asn Gln Glu Arg Ile Val Asp Val 245 250 255 Ala Gly Pro Gly Gly Trp Asn Asp Pro Asp Met Leu Val Ile Gly Asn 260 265 270 Phe Gly Leu Ser Trp Asn Gln Gln Val Thr Gln Met Ala Leu Trp Ala 275 280 285 Ile Met Ala Ala Pro Leu Phe Met Ser Asn Asp Leu Arg His Ile Ser 290 295 300 Pro Gln Ala Lys Ala Leu Leu Gln Asp Lys Asp Val Ile Ala Ile Asn 305 310 315 320 Gln Asp Pro Leu Gly Lys Gln Gly Tyr Gln Leu Arg Gln Gly Asp Asn 325 330 335 Phe Glu Val Trp Glu Arg Pro Leu Ser Gly Leu Ala Trp Ala Val Ala 340 345 350 Met Ile Asn Arg Gln Glu Ile Gly Gly Pro Arg Ser Tyr Thr Ile Ala 355 360 365 Val Ala Ser Leu Gly Lys Gly Val Ala Cys Asn Pro Ala Cys Phe Ile 370 375 380 Thr Gln Leu Leu Pro Val Lys Arg Lys Leu Gly Phe Tyr Glu Trp Thr 385 390 395 400 Ser Arg Leu Arg Ser His Ile Asn Pro Thr Gly Thr Val Leu Leu Gln 405 410 415 Leu Glu Asn Thr Met Gln Met Ser Leu Ser Glu Lys Asp Glu Leu 420 425 430 11 1266 DNA Homo sapiens CDS (1)...(1266) 11 atg cag ctg agg aac cca gaa cta cat ctg ggc tgc gcg ctt gcg ctt 48 Met Gln Leu Arg Asn Pro Glu Leu His Leu Gly Cys Ala Leu Ala Leu 1 5 10 15 cgc ttc ctg gcc ctc gtt tcc tgg gac atc cct ggg gct aga gca ctg 96 Arg Phe Leu Ala Leu Val Ser Trp Asp Ile Pro Gly Ala Arg Ala Leu 20 25 30 gac aat gga ttg gca agg acg cct acc atg ggc tgg ctg cac tgg gag 144 Asp Asn Gly Leu Ala Arg Thr Pro Thr Met Gly Trp Leu His Trp Glu 35 40 45 cgc ttc atg tgc aac ctt gac tgc cag gaa gag cca gat tcc tgc atc 192 Arg Phe Met Cys Asn Leu Asp Cys Gln Glu Glu Pro Asp Ser Cys Ile 50 55 60 agt gag aag ctc ttc atg gag atg gca gag ctc atg gtc tca gaa ggc 240 Ser Glu Lys Leu Phe Met Glu Met Ala Glu Leu Met Val Ser Glu Gly 65 70 75 80 tgg aag gat gca ggt tat gag tac ctc tgc att gat gac tgt tgg atg 288 Trp Lys Asp Ala Gly Tyr Glu Tyr Leu Cys Ile Asp Asp Cys Trp Met 85 90 95 gct ccc caa aga gat tca gaa ggc aga ctt cag gca gac cct cag cgc 336 Ala Pro Gln Arg Asp Ser Glu Gly Arg Leu Gln Ala Asp Pro Gln Arg 100 105 110 ttt cct cat ggg att cgc cag cta gct aat tat gtt cac agc aaa gga 384 Phe Pro His Gly Ile Arg Gln Leu Ala Asn Tyr Val His Ser Lys Gly 115 120 125 ctg aag cta ggg att tat gca gat gtt gga aat aaa acc tgc gca ggc 432 Leu Lys Leu Gly Ile Tyr Ala Asp Val Gly Asn Lys Thr Cys Ala Gly 130 135 140 ttc cct ggg agt ttt gga tac tac gac att gat gcc cag acc ttt gct 480 Phe Pro Gly Ser Phe Gly Tyr Tyr Asp Ile Asp Ala Gln Thr Phe Ala 145 150 155 160 gac tgg gga gta gat ctg cta aaa ttt gat ggt tgt tac tgt gac agt 528 Asp Trp Gly Val Asp Leu Leu Lys Phe Asp Gly Cys Tyr Cys Asp Ser 165 170 175 ttg gaa aat ttg gca gat ggt tat aag cac atg tcc ttg gcc ctg aat 576 Leu Glu Asn Leu Ala Asp Gly Tyr Lys His Met Ser Leu Ala Leu Asn 180 185 190 agg act ggc aga agc att gtg tac tcc tgt gag tgg cct ctt tat atg 624 Arg Thr Gly Arg Ser Ile Val Tyr Ser Cys Glu Trp Pro Leu Tyr Met 195 200 205 tgg ccc ttt caa aag ccc aat tat aca gaa atc cga cag tac tgc aat 672 Trp Pro Phe Gln Lys Pro Asn Tyr Thr Glu Ile Arg Gln Tyr Cys Asn 210 215 220 cac tgg cga aat ttt gct gac att gat gat tcc tgg aaa agt ata aag 720 His Trp Arg Asn Phe Ala Asp Ile Asp Asp Ser Trp Lys Ser Ile Lys 225 230 235 240 agt atc ttg gac tgg aca tct ttt aac cag gag aga att gtt gat gtt 768 Ser Ile Leu Asp Trp Thr Ser Phe Asn Gln Glu Arg Ile Val Asp Val 245 250 255 gct gga cca ggg ggt tgg aat gac cca gat atg tta gtg att ggc aac 816 Ala Gly Pro Gly Gly Trp Asn Asp Pro Asp Met Leu Val Ile Gly Asn 260 265 270 ttt ggc ctc agc tgg aat cag caa gta act cag atg gcc ctc tgg gct 864 Phe Gly Leu Ser Trp Asn Gln Gln Val Thr Gln Met Ala Leu Trp Ala 275 280 285 atc atg gct gct cct tta ttc atg tct aat gac ctc cga cac atc agc 912 Ile Met Ala Ala Pro Leu Phe Met Ser Asn Asp Leu Arg His Ile Ser 290 295 300 cct caa gcc aaa gct ctc ctt cag gat aag gac gta att gcc atc aat 960 Pro Gln Ala Lys Ala Leu Leu Gln Asp Lys Asp Val Ile Ala Ile Asn 305 310 315 320 cag gac ccc ttg ggc aag caa ggg tac cag ctt aga cag gga gac aac 1008 Gln Asp Pro Leu Gly Lys Gln Gly Tyr Gln Leu Arg Gln Gly Asp Asn 325 330 335 ttt gaa gtg tgg gaa cga cct ctc tca ggc tta gcc tgg gct gta gct 1056 Phe Glu Val Trp Glu Arg Pro Leu Ser Gly Leu Ala Trp Ala Val Ala 340 345 350 atg ata aac cgg cag gag att ggt gga cct cgc tct tat acc atc gca 1104 Met Ile Asn Arg Gln Glu Ile Gly Gly Pro Arg Ser Tyr Thr Ile Ala 355 360 365 gtt gct tcc ctg ggt aaa gga gtg gcc tgt aat cct gcc tgc ttc atc 1152 Val Ala Ser Leu Gly Lys Gly Val Ala Cys Asn Pro Ala Cys Phe Ile 370 375 380 aca cag ctc ctc cct gtg aaa agg aag cta ggg ttc tat gaa tgg act 1200 Thr Gln Leu Leu Pro Val Lys Arg Lys Leu Gly Phe Tyr Glu Trp Thr 385 390 395 400 tca agg tta aga agt cac ata aat ccc aca ggc act gtt ttg ctt cag 1248 Ser Arg Leu Arg Ser His Ile Asn Pro Thr Gly Thr Val Leu Leu Gln 405 410 415 cta gaa aac aca atg taa 1266 Leu Glu Asn Thr Met * 420 12 421 PRT Homo sapiens 12 Met Gln Leu Arg Asn Pro Glu Leu His Leu Gly Cys Ala Leu Ala Leu 1 5 10 15 Arg Phe Leu Ala Leu Val Ser Trp Asp Ile Pro Gly Ala Arg Ala Leu 20 25 30 Asp Asn Gly Leu Ala Arg Thr Pro Thr Met Gly Trp Leu His Trp Glu 35 40 45 Arg Phe Met Cys Asn Leu Asp Cys Gln Glu Glu Pro Asp Ser Cys Ile 50 55 60 Ser Glu Lys Leu Phe Met Glu Met Ala Glu Leu Met Val Ser Glu Gly 65 70 75 80 Trp Lys Asp Ala Gly Tyr Glu Tyr Leu Cys Ile Asp Asp Cys Trp Met 85 90 95 Ala Pro Gln Arg Asp Ser Glu Gly Arg Leu Gln Ala Asp Pro Gln Arg 100 105 110 Phe Pro His Gly Ile Arg Gln Leu Ala Asn Tyr Val His Ser Lys Gly 115 120 125 Leu Lys Leu Gly Ile Tyr Ala Asp Val Gly Asn Lys Thr Cys Ala Gly 130 135 140 Phe Pro Gly Ser Phe Gly Tyr Tyr Asp Ile Asp Ala Gln Thr Phe Ala 145 150 155 160 Asp Trp Gly Val Asp Leu Leu Lys Phe Asp Gly Cys Tyr Cys Asp Ser 165 170 175 Leu Glu Asn Leu Ala Asp Gly Tyr Lys His Met Ser Leu Ala Leu Asn 180 185 190 Arg Thr Gly Arg Ser Ile Val Tyr Ser Cys Glu Trp Pro Leu Tyr Met 195 200 205 Trp Pro Phe Gln Lys Pro Asn Tyr Thr Glu Ile Arg Gln Tyr Cys Asn 210 215 220 His Trp Arg Asn Phe Ala Asp Ile Asp Asp Ser Trp Lys Ser Ile Lys 225 230 235 240 Ser Ile Leu Asp Trp Thr Ser Phe Asn Gln Glu Arg Ile Val Asp Val 245 250 255 Ala Gly Pro Gly Gly Trp Asn Asp Pro Asp Met Leu Val Ile Gly Asn 260 265 270 Phe Gly Leu Ser Trp Asn Gln Gln Val Thr Gln Met Ala Leu Trp Ala 275 280 285 Ile Met Ala Ala Pro Leu Phe Met Ser Asn Asp Leu Arg His Ile Ser 290 295 300 Pro Gln Ala Lys Ala Leu Leu Gln Asp Lys Asp Val Ile Ala Ile Asn 305 310 315 320 Gln Asp Pro Leu Gly Lys Gln Gly Tyr Gln Leu Arg Gln Gly Asp Asn 325 330 335 Phe Glu Val Trp Glu Arg Pro Leu Ser Gly Leu Ala Trp Ala Val Ala 340 345 350 Met Ile Asn Arg Gln Glu Ile Gly Gly Pro Arg Ser Tyr Thr Ile Ala 355 360 365 Val Ala Ser Leu Gly Lys Gly Val Ala Cys Asn Pro Ala Cys Phe Ile 370 375 380 Thr Gln Leu Leu Pro Val Lys Arg Lys Leu Gly Phe Tyr Glu Trp Thr 385 390 395 400 Ser Arg Leu Arg Ser His Ile Asn Pro Thr Gly Thr Val Leu Leu Gln 405 410 415 Leu Glu Asn Thr Met 420 13 1284 DNA Homo sapiens CDS (1)...(1284) 13 atg cag ctg agg aac cca gaa cta cat ctg ggc tgc gcg ctt gcg ctt 48 Met Gln Leu Arg Asn Pro Glu Leu His Leu Gly Cys Ala Leu Ala Leu 1 5 10 15 cgc ttc ctg gcc ctc gtt tcc tgg gac atc cct ggg gct aga gca ctg 96 Arg Phe Leu Ala Leu Val Ser Trp Asp Ile Pro Gly Ala Arg Ala Leu 20 25 30 gac aat gga ttg gca agg acg cct acc atg ggc tgg ctg cac tgg gag 144 Asp Asn Gly Leu Ala Arg Thr Pro Thr Met Gly Trp Leu His Trp Glu 35 40 45 cgc ttc atg tgc aac ctt gac tgc cag gaa gag cca gat tcc tgc atc 192 Arg Phe Met Cys Asn Leu Asp Cys Gln Glu Glu Pro Asp Ser Cys Ile 50 55 60 agt gag aag ctc ttc atg gag atg gca gag ctc atg gtc tca gaa ggc 240 Ser Glu Lys Leu Phe Met Glu Met Ala Glu Leu Met Val Ser Glu Gly 65 70 75 80 tgg aag gat gca ggt tat gag tac ctc tgc att gat gac tgt tgg atg 288 Trp Lys Asp Ala Gly Tyr Glu Tyr Leu Cys Ile Asp Asp Cys Trp Met 85 90 95 gct ccc caa aga gat tca gaa ggc aga ctt cag gca gac cct cag cgc 336 Ala Pro Gln Arg Asp Ser Glu Gly Arg Leu Gln Ala Asp Pro Gln Arg 100 105 110 ttt cct cat ggg att cgc cag cta gct aat tat gtt cac agc aaa gga 384 Phe Pro His Gly Ile Arg Gln Leu Ala Asn Tyr Val His Ser Lys Gly 115 120 125 ctg aag cta ggg att tat gca gat gtt gga aat aaa acc tgc gca ggc 432 Leu Lys Leu Gly Ile Tyr Ala Asp Val Gly Asn Lys Thr Cys Ala Gly 130 135 140 ttc cct ggg agt ttt gga tac tac gac att gat gcc cag acc ttt gct 480 Phe Pro Gly Ser Phe Gly Tyr Tyr Asp Ile Asp Ala Gln Thr Phe Ala 145 150 155 160 gac tgg gga gta gat ctg cta aaa ttt gat ggt tgt tac tgt gac agt 528 Asp Trp Gly Val Asp Leu Leu Lys Phe Asp Gly Cys Tyr Cys Asp Ser 165 170 175 ttg gaa aat ttg gca gat ggt tat aag cac atg tcc ttg gcc ctg aat 576 Leu Glu Asn Leu Ala Asp Gly Tyr Lys His Met Ser Leu Ala Leu Asn 180 185 190 agg act ggc aga agc att gtg tac tcc tgt gag tgg cct ctt tat atg 624 Arg Thr Gly Arg Ser Ile Val Tyr Ser Cys Glu Trp Pro Leu Tyr Met 195 200 205 tgg ccc ttt caa aag ccc aat tat aca gaa atc cga cag tac tgc aat 672 Trp Pro Phe Gln Lys Pro Asn Tyr Thr Glu Ile Arg Gln Tyr Cys Asn 210 215 220 cac tgg cga aat ttt gct gac att gat gat tcc tgg aaa agt ata aag 720 His Trp Arg Asn Phe Ala Asp Ile Asp Asp Ser Trp Lys Ser Ile Lys 225 230 235 240 agt atc ttg gac tgg aca tct ttt aac cag gag aga att gtt gat gtt 768 Ser Ile Leu Asp Trp Thr Ser Phe Asn Gln Glu Arg Ile Val Asp Val 245 250 255 gct gga cca ggg ggt tgg aat gac cca gat atg tta gtg att ggc aac 816 Ala Gly Pro Gly Gly Trp Asn Asp Pro Asp Met Leu Val Ile Gly Asn 260 265 270 ttt ggc ctc agc tgg aat cag caa gta act cag atg gcc ctc tgg gct 864 Phe Gly Leu Ser Trp Asn Gln Gln Val Thr Gln Met Ala Leu Trp Ala 275 280 285 atc atg gct gct cct tta ttc atg tct aat gac ctc cga cac atc agc 912 Ile Met Ala Ala Pro Leu Phe Met Ser Asn Asp Leu Arg His Ile Ser 290 295 300 cct caa gcc aaa gct ctc ctt cag gat aag gac gta att gcc atc aat 960 Pro Gln Ala Lys Ala Leu Leu Gln Asp Lys Asp Val Ile Ala Ile Asn 305 310 315 320 cag gac ccc ttg ggc aag caa ggg tac cag ctt aga cag gga gac aac 1008 Gln Asp Pro Leu Gly Lys Gln Gly Tyr Gln Leu Arg Gln Gly Asp Asn 325 330 335 ttt gaa gtg tgg gaa cga cct ctc tca ggc tta gcc tgg gct gta gct 1056 Phe Glu Val Trp Glu Arg Pro Leu Ser Gly Leu Ala Trp Ala Val Ala 340 345 350 atg ata aac cgg cag gag att ggt gga cct cgc tct tat acc atc gca 1104 Met Ile Asn Arg Gln Glu Ile Gly Gly Pro Arg Ser Tyr Thr Ile Ala 355 360 365 gtt gct tcc ctg ggt aaa gga gtg gcc tgt aat cct gcc tgc ttc atc 1152 Val Ala Ser Leu Gly Lys Gly Val Ala Cys Asn Pro Ala Cys Phe Ile 370 375 380 aca cag ctc ctc cct gtg aaa agg aag cta ggg ttc tat gaa tgg act 1200 Thr Gln Leu Leu Pro Val Lys Arg Lys Leu Gly Phe Tyr Glu Trp Thr 385 390 395 400 tca agg tta aga agt cac ata aat ccc aca ggc act gtt ttg ctt cag 1248 Ser Arg Leu Arg Ser His Ile Asn Pro Thr Gly Thr Val Leu Leu Gln 405 410 415 cta gaa aac aca atg tct gaa aag gac gaa tta tga 1284 Leu Glu Asn Thr Met Ser Glu Lys Asp Glu Leu * 420 425 14 427 PRT Homo sapiens 14 Met Gln Leu Arg Asn Pro Glu Leu His Leu Gly Cys Ala Leu Ala Leu 1 5 10 15 Arg Phe Leu Ala Leu Val Ser Trp Asp Ile Pro Gly Ala Arg Ala Leu 20 25 30 Asp Asn Gly Leu Ala Arg Thr Pro Thr Met Gly Trp Leu His Trp Glu 35 40 45 Arg Phe Met Cys Asn Leu Asp Cys Gln Glu Glu Pro Asp Ser Cys Ile 50 55 60 Ser Glu Lys Leu Phe Met Glu Met Ala Glu Leu Met Val Ser Glu Gly 65 70 75 80 Trp Lys Asp Ala Gly Tyr Glu Tyr Leu Cys Ile Asp Asp Cys Trp Met 85 90 95 Ala Pro Gln Arg Asp Ser Glu Gly Arg Leu Gln Ala Asp Pro Gln Arg 100 105 110 Phe Pro His Gly Ile Arg Gln Leu Ala Asn Tyr Val His Ser Lys Gly 115 120 125 Leu Lys Leu Gly Ile Tyr Ala Asp Val Gly Asn Lys Thr Cys Ala Gly 130 135 140 Phe Pro Gly Ser Phe Gly Tyr Tyr Asp Ile Asp Ala Gln Thr Phe Ala 145 150 155 160 Asp Trp Gly Val Asp Leu Leu Lys Phe Asp Gly Cys Tyr Cys Asp Ser 165 170 175 Leu Glu Asn Leu Ala Asp Gly Tyr Lys His Met Ser Leu Ala Leu Asn 180 185 190 Arg Thr Gly Arg Ser Ile Val Tyr Ser Cys Glu Trp Pro Leu Tyr Met 195 200 205 Trp Pro Phe Gln Lys Pro Asn Tyr Thr Glu Ile Arg Gln Tyr Cys Asn 210 215 220 His Trp Arg Asn Phe Ala Asp Ile Asp Asp Ser Trp Lys Ser Ile Lys 225 230 235 240 Ser Ile Leu Asp Trp Thr Ser Phe Asn Gln Glu Arg Ile Val Asp Val 245 250 255 Ala Gly Pro Gly Gly Trp Asn Asp Pro Asp Met Leu Val Ile Gly Asn 260 265 270 Phe Gly Leu Ser Trp Asn Gln Gln Val Thr Gln Met Ala Leu Trp Ala 275 280 285 Ile Met Ala Ala Pro Leu Phe Met Ser Asn Asp Leu Arg His Ile Ser 290 295 300 Pro Gln Ala Lys Ala Leu Leu Gln Asp Lys Asp Val Ile Ala Ile Asn 305 310 315 320 Gln Asp Pro Leu Gly Lys Gln Gly Tyr Gln Leu Arg Gln Gly Asp Asn 325 330 335 Phe Glu Val Trp Glu Arg Pro Leu Ser Gly Leu Ala Trp Ala Val Ala 340 345 350 Met Ile Asn Arg Gln Glu Ile Gly Gly Pro Arg Ser Tyr Thr Ile Ala 355 360 365 Val Ala Ser Leu Gly Lys Gly Val Ala Cys Asn Pro Ala Cys Phe Ile 370 375 380 Thr Gln Leu Leu Pro Val Lys Arg Lys Leu Gly Phe Tyr Glu Trp Thr 385 390 395 400 Ser Arg Leu Arg Ser His Ile Asn Pro Thr Gly Thr Val Leu Leu Gln 405 410 415 Leu Glu Asn Thr Met Ser Glu Lys Asp Glu Leu 420 425 15 1254 DNA Homo sapiens CDS (1)...(1254) 15 atg cag ctg agg aac cca gaa cta cat ctg ggc tgc gcg ctt gcg ctt 48 Met Gln Leu Arg Asn Pro Glu Leu His Leu Gly Cys Ala Leu Ala Leu 1 5 10 15 cgc ttc ctg gcc ctc gtt tcc tgg gac atc cct ggg gct aga gca ctg 96 Arg Phe Leu Ala Leu Val Ser Trp Asp Ile Pro Gly Ala Arg Ala Leu 20 25 30 gac aat gga ttg gca agg acg cct acc atg ggc tgg ctg cac tgg gag 144 Asp Asn Gly Leu Ala Arg Thr Pro Thr Met Gly Trp Leu His Trp Glu 35 40 45 cgc ttc atg tgc aac ctt gac tgc cag gaa gag cca gat tcc tgc atc 192 Arg Phe Met Cys Asn Leu Asp Cys Gln Glu Glu Pro Asp Ser Cys Ile 50 55 60 agt gag aag ctc ttc atg gag atg gca gag ctc atg gtc tca gaa ggc 240 Ser Glu Lys Leu Phe Met Glu Met Ala Glu Leu Met Val Ser Glu Gly 65 70 75 80 tgg aag gat gca ggt tat gag tac ctc tgc att gat gac tgt tgg atg 288 Trp Lys Asp Ala Gly Tyr Glu Tyr Leu Cys Ile Asp Asp Cys Trp Met 85 90 95 gct ccc caa aga gat tca gaa ggc aga ctt cag gca gac cct cag cgc 336 Ala Pro Gln Arg Asp Ser Glu Gly Arg Leu Gln Ala Asp Pro Gln Arg 100 105 110 ttt cct cat ggg att cgc cag cta gct aat tat gtt cac agc aaa gga 384 Phe Pro His Gly Ile Arg Gln Leu Ala Asn Tyr Val His Ser Lys Gly 115 120 125 ctg aag cta ggg att tat gca gat gtt gga aat aaa acc tgc gca ggc 432 Leu Lys Leu Gly Ile Tyr Ala Asp Val Gly Asn Lys Thr Cys Ala Gly 130 135 140 ttc cct ggg agt ttt gga tac tac gac att gat gcc cag acc ttt gct 480 Phe Pro Gly Ser Phe Gly Tyr Tyr Asp Ile Asp Ala Gln Thr Phe Ala 145 150 155 160 gac tgg gga gta gat ctg cta aaa ttt gat ggt tgt tac tgt gac agt 528 Asp Trp Gly Val Asp Leu Leu Lys Phe Asp Gly Cys Tyr Cys Asp Ser 165 170 175 ttg gaa aat ttg gca gat ggt tat aag cac atg tcc ttg gcc ctg aat 576 Leu Glu Asn Leu Ala Asp Gly Tyr Lys His Met Ser Leu Ala Leu Asn 180 185 190 agg act ggc aga agc att gtg tac tcc tgt gag tgg cct ctt tat atg 624 Arg Thr Gly Arg Ser Ile Val Tyr Ser Cys Glu Trp Pro Leu Tyr Met 195 200 205 tgg ccc ttt caa aag ccc aat tat aca gaa atc cga cag tac tgc aat 672 Trp Pro Phe Gln Lys Pro Asn Tyr Thr Glu Ile Arg Gln Tyr Cys Asn 210 215 220 cac tgg cga aat ttt gct gac att gat gat tcc tgg aaa agt ata aag 720 His Trp Arg Asn Phe Ala Asp Ile Asp Asp Ser Trp Lys Ser Ile Lys 225 230 235 240 agt atc ttg gac tgg aca tct ttt aac cag gag aga att gtt gat gtt 768 Ser Ile Leu Asp Trp Thr Ser Phe Asn Gln Glu Arg Ile Val Asp Val 245 250 255 gct gga cca ggg ggt tgg aat gac cca gat atg tta gtg att ggc aac 816 Ala Gly Pro Gly Gly Trp Asn Asp Pro Asp Met Leu Val Ile Gly Asn 260 265 270 ttt ggc ctc agc tgg aat cag caa gta act cag atg gcc ctc tgg gct 864 Phe Gly Leu Ser Trp Asn Gln Gln Val Thr Gln Met Ala Leu Trp Ala 275 280 285 atc atg gct gct cct tta ttc atg tct aat gac ctc cga cac atc agc 912 Ile Met Ala Ala Pro Leu Phe Met Ser Asn Asp Leu Arg His Ile Ser 290 295 300 cct caa gcc aaa gct ctc ctt cag gat aag gac gta att gcc atc aat 960 Pro Gln Ala Lys Ala Leu Leu Gln Asp Lys Asp Val Ile Ala Ile Asn 305 310 315 320 cag gac ccc ttg ggc aag caa ggg tac cag ctt aga cag gga gac aac 1008 Gln Asp Pro Leu Gly Lys Gln Gly Tyr Gln Leu Arg Gln Gly Asp Asn 325 330 335 ttt gaa gtg tgg gaa cga cct ctc tca ggc tta gcc tgg gct gta gct 1056 Phe Glu Val Trp Glu Arg Pro Leu Ser Gly Leu Ala Trp Ala Val Ala 340 345 350 atg ata aac cgg cag gag att ggt gga cct cgc tct tat acc atc gca 1104 Met Ile Asn Arg Gln Glu Ile Gly Gly Pro Arg Ser Tyr Thr Ile Ala 355 360 365 gtt gct tcc ctg ggt aaa gga gtg gcc tgt aat cct gcc tgc ttc atc 1152 Val Ala Ser Leu Gly Lys Gly Val Ala Cys Asn Pro Ala Cys Phe Ile 370 375 380 aca cag ctc ctc cct gtg aaa agg aag cta ggg ttc tat gaa tgg act 1200 Thr Gln Leu Leu Pro Val Lys Arg Lys Leu Gly Phe Tyr Glu Trp Thr 385 390 395 400 tca agg tta aga agt cac ata aat ccc aca ggc act gtt ttg ctt cag 1248 Ser Arg Leu Arg Ser His Ile Asn Pro Thr Gly Thr Val Leu Leu Gln 405 410 415 cta taa 1254 Leu * 16 417 PRT Homo sapiens 16 Met Gln Leu Arg Asn Pro Glu Leu His Leu Gly Cys Ala Leu Ala Leu 1 5 10 15 Arg Phe Leu Ala Leu Val Ser Trp Asp Ile Pro Gly Ala Arg Ala Leu 20 25 30 Asp Asn Gly Leu Ala Arg Thr Pro Thr Met Gly Trp Leu His Trp Glu 35 40 45 Arg Phe Met Cys Asn Leu Asp Cys Gln Glu Glu Pro Asp Ser Cys Ile 50 55 60 Ser Glu Lys Leu Phe Met Glu Met Ala Glu Leu Met Val Ser Glu Gly 65 70 75 80 Trp Lys Asp Ala Gly Tyr Glu Tyr Leu Cys Ile Asp Asp Cys Trp Met 85 90 95 Ala Pro Gln Arg Asp Ser Glu Gly Arg Leu Gln Ala Asp Pro Gln Arg 100 105 110 Phe Pro His Gly Ile Arg Gln Leu Ala Asn Tyr Val His Ser Lys Gly 115 120 125 Leu Lys Leu Gly Ile Tyr Ala Asp Val Gly Asn Lys Thr Cys Ala Gly 130 135 140 Phe Pro Gly Ser Phe Gly Tyr Tyr Asp Ile Asp Ala Gln Thr Phe Ala 145 150 155 160 Asp Trp Gly Val Asp Leu Leu Lys Phe Asp Gly Cys Tyr Cys Asp Ser 165 170 175 Leu Glu Asn Leu Ala Asp Gly Tyr Lys His Met Ser Leu Ala Leu Asn 180 185 190 Arg Thr Gly Arg Ser Ile Val Tyr Ser Cys Glu Trp Pro Leu Tyr Met 195 200 205 Trp Pro Phe Gln Lys Pro Asn Tyr Thr Glu Ile Arg Gln Tyr Cys Asn 210 215 220 His Trp Arg Asn Phe Ala Asp Ile Asp Asp Ser Trp Lys Ser Ile Lys 225 230 235 240 Ser Ile Leu Asp Trp Thr Ser Phe Asn Gln Glu Arg Ile Val Asp Val 245 250 255 Ala Gly Pro Gly Gly Trp Asn Asp Pro Asp Met Leu Val Ile Gly Asn 260 265 270 Phe Gly Leu Ser Trp Asn Gln Gln Val Thr Gln Met Ala Leu Trp Ala 275 280 285 Ile Met Ala Ala Pro Leu Phe Met Ser Asn Asp Leu Arg His Ile Ser 290 295 300 Pro Gln Ala Lys Ala Leu Leu Gln Asp Lys Asp Val Ile Ala Ile Asn 305 310 315 320 Gln Asp Pro Leu Gly Lys Gln Gly Tyr Gln Leu Arg Gln Gly Asp Asn 325 330 335 Phe Glu Val Trp Glu Arg Pro Leu Ser Gly Leu Ala Trp Ala Val Ala 340 345 350 Met Ile Asn Arg Gln Glu Ile Gly Gly Pro Arg Ser Tyr Thr Ile Ala 355 360 365 Val Ala Ser Leu Gly Lys Gly Val Ala Cys Asn Pro Ala Cys Phe Ile 370 375 380 Thr Gln Leu Leu Pro Val Lys Arg Lys Leu Gly Phe Tyr Glu Trp Thr 385 390 395 400 Ser Arg Leu Arg Ser His Ile Asn Pro Thr Gly Thr Val Leu Leu Gln 405 410 415 Leu 17 1272 DNA Homo sapiens CDS (1)...(1272) 17 atg cag ctg agg aac cca gaa cta cat ctg ggc tgc gcg ctt gcg ctt 48 Met Gln Leu Arg Asn Pro Glu Leu His Leu Gly Cys Ala Leu Ala Leu 1 5 10 15 cgc ttc ctg gcc ctc gtt tcc tgg gac atc cct ggg gct aga gca ctg 96 Arg Phe Leu Ala Leu Val Ser Trp Asp Ile Pro Gly Ala Arg Ala Leu 20 25 30 gac aat gga ttg gca agg acg cct acc atg ggc tgg ctg cac tgg gag 144 Asp Asn Gly Leu Ala Arg Thr Pro Thr Met Gly Trp Leu His Trp Glu 35 40 45 cgc ttc atg tgc aac ctt gac tgc cag gaa gag cca gat tcc tgc atc 192 Arg Phe Met Cys Asn Leu Asp Cys Gln Glu Glu Pro Asp Ser Cys Ile 50 55 60 agt gag aag ctc ttc atg gag atg gca gag ctc atg gtc tca gaa ggc 240 Ser Glu Lys Leu Phe Met Glu Met Ala Glu Leu Met Val Ser Glu Gly 65 70 75 80 tgg aag gat gca ggt tat gag tac ctc tgc att gat gac tgt tgg atg 288 Trp Lys Asp Ala Gly Tyr Glu Tyr Leu Cys Ile Asp Asp Cys Trp Met 85 90 95 gct ccc caa aga gat tca gaa ggc aga ctt cag gca gac cct cag cgc 336 Ala Pro Gln Arg Asp Ser Glu Gly Arg Leu Gln Ala Asp Pro Gln Arg 100 105 110 ttt cct cat ggg att cgc cag cta gct aat tat gtt cac agc aaa gga 384 Phe Pro His Gly Ile Arg Gln Leu Ala Asn Tyr Val His Ser Lys Gly 115 120 125 ctg aag cta ggg att tat gca gat gtt gga aat aaa acc tgc gca ggc 432 Leu Lys Leu Gly Ile Tyr Ala Asp Val Gly Asn Lys Thr Cys Ala Gly 130 135 140 ttc cct ggg agt ttt gga tac tac gac att gat gcc cag acc ttt gct 480 Phe Pro Gly Ser Phe Gly Tyr Tyr Asp Ile Asp Ala Gln Thr Phe Ala 145 150 155 160 gac tgg gga gta gat ctg cta aaa ttt gat ggt tgt tac tgt gac agt 528 Asp Trp Gly Val Asp Leu Leu Lys Phe Asp Gly Cys Tyr Cys Asp Ser 165 170 175 ttg gaa aat ttg gca gat ggt tat aag cac atg tcc ttg gcc ctg aat 576 Leu Glu Asn Leu Ala Asp Gly Tyr Lys His Met Ser Leu Ala Leu Asn 180 185 190 agg act ggc aga agc att gtg tac tcc tgt gag tgg cct ctt tat atg 624 Arg Thr Gly Arg Ser Ile Val Tyr Ser Cys Glu Trp Pro Leu Tyr Met 195 200 205 tgg ccc ttt caa aag ccc aat tat aca gaa atc cga cag tac tgc aat 672 Trp Pro Phe Gln Lys Pro Asn Tyr Thr Glu Ile Arg Gln Tyr Cys Asn 210 215 220 cac tgg cga aat ttt gct gac att gat gat tcc tgg aaa agt ata aag 720 His Trp Arg Asn Phe Ala Asp Ile Asp Asp Ser Trp Lys Ser Ile Lys 225 230 235 240 agt atc ttg gac tgg aca tct ttt aac cag gag aga att gtt gat gtt 768 Ser Ile Leu Asp Trp Thr Ser Phe Asn Gln Glu Arg Ile Val Asp Val 245 250 255 gct gga cca ggg ggt tgg aat gac cca gat atg tta gtg att ggc aac 816 Ala Gly Pro Gly Gly Trp Asn Asp Pro Asp Met Leu Val Ile Gly Asn 260 265 270 ttt ggc ctc agc tgg aat cag caa gta act cag atg gcc ctc tgg gct 864 Phe Gly Leu Ser Trp Asn Gln Gln Val Thr Gln Met Ala Leu Trp Ala 275 280 285 atc atg gct gct cct tta ttc atg tct aat gac ctc cga cac atc agc 912 Ile Met Ala Ala Pro Leu Phe Met Ser Asn Asp Leu Arg His Ile Ser 290 295 300 cct caa gcc aaa gct ctc ctt cag gat aag gac gta att gcc atc aat 960 Pro Gln Ala Lys Ala Leu Leu Gln Asp Lys Asp Val Ile Ala Ile Asn 305 310 315 320 cag gac ccc ttg ggc aag caa ggg tac cag ctt aga cag gga gac aac 1008 Gln Asp Pro Leu Gly Lys Gln Gly Tyr Gln Leu Arg Gln Gly Asp Asn 325 330 335 ttt gaa gtg tgg gaa cga cct ctc tca ggc tta gcc tgg gct gta gct 1056 Phe Glu Val Trp Glu Arg Pro Leu Ser Gly Leu Ala Trp Ala Val Ala 340 345 350 atg ata aac cgg cag gag att ggt gga cct cgc tct tat acc atc gca 1104 Met Ile Asn Arg Gln Glu Ile Gly Gly Pro Arg Ser Tyr Thr Ile Ala 355 360 365 gtt gct tcc ctg ggt aaa gga gtg gcc tgt aat cct gcc tgc ttc atc 1152 Val Ala Ser Leu Gly Lys Gly Val Ala Cys Asn Pro Ala Cys Phe Ile 370 375 380 aca cag ctc ctc cct gtg aaa agg aag cta ggg ttc tat gaa tgg act 1200 Thr Gln Leu Leu Pro Val Lys Arg Lys Leu Gly Phe Tyr Glu Trp Thr 385 390 395 400 tca agg tta aga agt cac ata aat ccc aca ggc act gtt ttg ctt cag 1248 Ser Arg Leu Arg Ser His Ile Asn Pro Thr Gly Thr Val Leu Leu Gln 405 410 415 cta tct gaa aag gac gaa tta tga 1272 Leu Ser Glu Lys Asp Glu Leu * 420 18 423 PRT Homo sapiens 18 Met Gln Leu Arg Asn Pro Glu Leu His Leu Gly Cys Ala Leu Ala Leu 1 5 10 15 Arg Phe Leu Ala Leu Val Ser Trp Asp Ile Pro Gly Ala Arg Ala Leu 20 25 30 Asp Asn Gly Leu Ala Arg Thr Pro Thr Met Gly Trp Leu His Trp Glu 35 40 45 Arg Phe Met Cys Asn Leu Asp Cys Gln Glu Glu Pro Asp Ser Cys Ile 50 55 60 Ser Glu Lys Leu Phe Met Glu Met Ala Glu Leu Met Val Ser Glu Gly 65 70 75 80 Trp Lys Asp Ala Gly Tyr Glu Tyr Leu Cys Ile Asp Asp Cys Trp Met 85 90 95 Ala Pro Gln Arg Asp Ser Glu Gly Arg Leu Gln Ala Asp Pro Gln Arg 100 105 110 Phe Pro His Gly Ile Arg Gln Leu Ala Asn Tyr Val His Ser Lys Gly 115 120 125 Leu Lys Leu Gly Ile Tyr Ala Asp Val Gly Asn Lys Thr Cys Ala Gly 130 135 140 Phe Pro Gly Ser Phe Gly Tyr Tyr Asp Ile Asp Ala Gln Thr Phe Ala 145 150 155 160 Asp Trp Gly Val Asp Leu Leu Lys Phe Asp Gly Cys Tyr Cys Asp Ser 165 170 175 Leu Glu Asn Leu Ala Asp Gly Tyr Lys His Met Ser Leu Ala Leu Asn 180 185 190 Arg Thr Gly Arg Ser Ile Val Tyr Ser Cys Glu Trp Pro Leu Tyr Met 195 200 205 Trp Pro Phe Gln Lys Pro Asn Tyr Thr Glu Ile Arg Gln Tyr Cys Asn 210 215 220 His Trp Arg Asn Phe Ala Asp Ile Asp Asp Ser Trp Lys Ser Ile Lys 225 230 235 240 Ser Ile Leu Asp Trp Thr Ser Phe Asn Gln Glu Arg Ile Val Asp Val 245 250 255 Ala Gly Pro Gly Gly Trp Asn Asp Pro Asp Met Leu Val Ile Gly Asn 260 265 270 Phe Gly Leu Ser Trp Asn Gln Gln Val Thr Gln Met Ala Leu Trp Ala 275 280 285 Ile Met Ala Ala Pro Leu Phe Met Ser Asn Asp Leu Arg His Ile Ser 290 295 300 Pro Gln Ala Lys Ala Leu Leu Gln Asp Lys Asp Val Ile Ala Ile Asn 305 310 315 320 Gln Asp Pro Leu Gly Lys Gln Gly Tyr Gln Leu Arg Gln Gly Asp Asn 325 330 335 Phe Glu Val Trp Glu Arg Pro Leu Ser Gly Leu Ala Trp Ala Val Ala 340 345 350 Met Ile Asn Arg Gln Glu Ile Gly Gly Pro Arg Ser Tyr Thr Ile Ala 355 360 365 Val Ala Ser Leu Gly Lys Gly Val Ala Cys Asn Pro Ala Cys Phe Ile 370 375 380 Thr Gln Leu Leu Pro Val Lys Arg Lys Leu Gly Phe Tyr Glu Trp Thr 385 390 395 400 Ser Arg Leu Arg Ser His Ile Asn Pro Thr Gly Thr Val Leu Leu Gln 405 410 415 Leu Ser Glu Lys Asp Glu Leu 420 19 1215 DNA Homo sapiens CDS (10)...(1215) 19 atgcagctg agg aac cca gaa cta cat ctg ggc tgc gcg ctt gcg ctt cgc 51 Arg Asn Pro Glu Leu His Leu Gly Cys Ala Leu Ala Leu Arg 1 5 10 ttc ctg gcc ctc gtt tcc tgg gac atc cct ggg gct aga gca ctg gac 99 Phe Leu Ala Leu Val Ser Trp Asp Ile Pro Gly Ala Arg Ala Leu Asp 15 20 25 30 aat gga ttg gca agg acg cct acc atg ggc tgg ctg cac tgg gag cgc 147 Asn Gly Leu Ala Arg Thr Pro Thr Met Gly Trp Leu His Trp Glu Arg 35 40 45 ttc atg tgc aac ctt gac tgc cag gaa gag cca gat tcc tgc atc agt 195 Phe Met Cys Asn Leu Asp Cys Gln Glu Glu Pro Asp Ser Cys Ile Ser 50 55 60 gag aag ctc ttc atg gag atg gca gag ctc atg gtc tca gaa ggc tgg 243 Glu Lys Leu Phe Met Glu Met Ala Glu Leu Met Val Ser Glu Gly Trp 65 70 75 aag gat gca ggt tat gag tac ctc tgc att gat gac tgt tgg atg gct 291 Lys Asp Ala Gly Tyr Glu Tyr Leu Cys Ile Asp Asp Cys Trp Met Ala 80 85 90 ccc caa aga gat tca gaa ggc aga ctt cag gca gac cct cag cgc ttt 339 Pro Gln Arg Asp Ser Glu Gly Arg Leu Gln Ala Asp Pro Gln Arg Phe 95 100 105 110 cct cat ggg att cgc cag cta gct aat tat gtt cac agc aaa gga ctg 387 Pro His Gly Ile Arg Gln Leu Ala Asn Tyr Val His Ser Lys Gly Leu 115 120 125 aag cta ggg att tat gca gat gtt gga aat aaa acc tgc gca ggc ttc 435 Lys Leu Gly Ile Tyr Ala Asp Val Gly Asn Lys Thr Cys Ala Gly Phe 130 135 140 cct ggg agt ttt gga tac tac gac att gat gcc cag acc ttt gct gac 483 Pro Gly Ser Phe Gly Tyr Tyr Asp Ile Asp Ala Gln Thr Phe Ala Asp 145 150 155 tgg gga gta gat ctg cta aaa ttt gat ggt tgt tac tgt gac agt ttg 531 Trp Gly Val Asp Leu Leu Lys Phe Asp Gly Cys Tyr Cys Asp Ser Leu 160 165 170 gaa aat ttg gca gat ggt tat aag cac atg tcc ttg gcc ctg aat agg 579 Glu Asn Leu Ala Asp Gly Tyr Lys His Met Ser Leu Ala Leu Asn Arg 175 180 185 190 act ggc aga agc att gtg tac tcc tgt gag tgg cct ctt tat atg tgg 627 Thr Gly Arg Ser Ile Val Tyr Ser Cys Glu Trp Pro Leu Tyr Met Trp 195 200 205 ccc ttt caa aag ccc aat tat aca gaa atc cga cag tac tgc aat cac 675 Pro Phe Gln Lys Pro Asn Tyr Thr Glu Ile Arg Gln Tyr Cys Asn His 210 215 220 tgg cga aat ttt gct gac att gat gat tcc tgg aaa agt ata aag agt 723 Trp Arg Asn Phe Ala Asp Ile Asp Asp Ser Trp Lys Ser Ile Lys Ser 225 230 235 atc ttg gac tgg aca tct ttt aac cag gag aga att gtt gat gtt gct 771 Ile Leu Asp Trp Thr Ser Phe Asn Gln Glu Arg Ile Val Asp Val Ala 240 245 250 gga cca ggg ggt tgg aat gac cca gat atg tta gtg att ggc aac ttt 819 Gly Pro Gly Gly Trp Asn Asp Pro Asp Met Leu Val Ile Gly Asn Phe 255 260 265 270 ggc ctc agc tgg aat cag caa gta act cag atg gcc ctc tgg gct atc 867 Gly Leu Ser Trp Asn Gln Gln Val Thr Gln Met Ala Leu Trp Ala Ile 275 280 285 atg gct gct cct tta ttc atg tct aat gac ctc cga cac atc agc cct 915 Met Ala Ala Pro Leu Phe Met Ser Asn Asp Leu Arg His Ile Ser Pro 290 295 300 caa gcc aaa gct ctc ctt cag gat aag gac gta att gcc atc aat cag 963 Gln Ala Lys Ala Leu Leu Gln Asp Lys Asp Val Ile Ala Ile Asn Gln 305 310 315 gac ccc ttg ggc aag caa ggg tac cag ctt aga cag gga gac aac ttt 1011 Asp Pro Leu Gly Lys Gln Gly Tyr Gln Leu Arg Gln Gly Asp Asn Phe 320 325 330 gaa gtg tgg gaa cga cct ctc tca ggc tta gcc tgg gct gta gct atg 1059 Glu Val Trp Glu Arg Pro Leu Ser Gly Leu Ala Trp Ala Val Ala Met 335 340 345 350 ata aac cgg cag gag att ggt gga cct cgc tct tat acc atc gca gtt 1107 Ile Asn Arg Gln Glu Ile Gly Gly Pro Arg Ser Tyr Thr Ile Ala Val 355 360 365 gct tcc ctg ggt aaa gga gtg gcc tgt aat cct gcc tgc ttc atc aca 1155 Ala Ser Leu Gly Lys Gly Val Ala Cys Asn Pro Ala Cys Phe Ile Thr 370 375 380 cag ctc ctc cct gtg aaa agg aag cta ggg ttc tat gaa tgg act tca 1203 Gln Leu Leu Pro Val Lys Arg Lys Leu Gly Phe Tyr Glu Trp Thr Ser 385 390 395 agg tta aga taa 1215 Arg Leu Arg * 400 20 401 PRT Homo sapiens 20 Arg Asn Pro Glu Leu His Leu Gly Cys Ala Leu Ala Leu Arg Phe Leu 1 5 10 15 Ala Leu Val Ser Trp Asp Ile Pro Gly Ala Arg Ala Leu Asp Asn Gly 20 25 30 Leu Ala Arg Thr Pro Thr Met Gly Trp Leu His Trp Glu Arg Phe Met 35 40 45 Cys Asn Leu Asp Cys Gln Glu Glu Pro Asp Ser Cys Ile Ser Glu Lys 50 55 60 Leu Phe Met Glu Met Ala Glu Leu Met Val Ser Glu Gly Trp Lys Asp 65 70 75 80 Ala Gly Tyr Glu Tyr Leu Cys Ile Asp Asp Cys Trp Met Ala Pro Gln 85 90 95 Arg Asp Ser Glu Gly Arg Leu Gln Ala Asp Pro Gln Arg Phe Pro His 100 105 110 Gly Ile Arg Gln Leu Ala Asn Tyr Val His Ser Lys Gly Leu Lys Leu 115 120 125 Gly Ile Tyr Ala Asp Val Gly Asn Lys Thr Cys Ala Gly Phe Pro Gly 130 135 140 Ser Phe Gly Tyr Tyr Asp Ile Asp Ala Gln Thr Phe Ala Asp Trp Gly 145 150 155 160 Val Asp Leu Leu Lys Phe Asp Gly Cys Tyr Cys Asp Ser Leu Glu Asn 165 170 175 Leu Ala Asp Gly Tyr Lys His Met Ser Leu Ala Leu Asn Arg Thr Gly 180 185 190 Arg Ser Ile Val Tyr Ser Cys Glu Trp Pro Leu Tyr Met Trp Pro Phe 195 200 205 Gln Lys Pro Asn Tyr Thr Glu Ile Arg Gln Tyr Cys Asn His Trp Arg 210 215 220 Asn Phe Ala Asp Ile Asp Asp Ser Trp Lys Ser Ile Lys Ser Ile Leu 225 230 235 240 Asp Trp Thr Ser Phe Asn Gln Glu Arg Ile Val Asp Val Ala Gly Pro 245 250 255 Gly Gly Trp Asn Asp Pro Asp Met Leu Val Ile Gly Asn Phe Gly Leu 260 265 270 Ser Trp Asn Gln Gln Val Thr Gln Met Ala Leu Trp Ala Ile Met Ala 275 280 285 Ala Pro Leu Phe Met Ser Asn Asp Leu Arg His Ile Ser Pro Gln Ala 290 295 300 Lys Ala Leu Leu Gln Asp Lys Asp Val Ile Ala Ile Asn Gln Asp Pro 305 310 315 320 Leu Gly Lys Gln Gly Tyr Gln Leu Arg Gln Gly Asp Asn Phe Glu Val 325 330 335 Trp Glu Arg Pro Leu Ser Gly Leu Ala Trp Ala Val Ala Met Ile Asn 340 345 350 Arg Gln Glu Ile Gly Gly Pro Arg Ser Tyr Thr Ile Ala Val Ala Ser 355 360 365 Leu Gly Lys Gly Val Ala Cys Asn Pro Ala Cys Phe Ile Thr Gln Leu 370 375 380 Leu Pro Val Lys Arg Lys Leu Gly Phe Tyr Glu Trp Thr Ser Arg Leu 385 390 395 400 Arg 21 1233 DNA Homo sapiens CDS (1)...(1233) 21 atg cag ctg agg aac cca gaa cta cat ctg ggc tgc gcg ctt gcg ctt 48 Met Gln Leu Arg Asn Pro Glu Leu His Leu Gly Cys Ala Leu Ala Leu 1 5 10 15 cgc ttc ctg gcc ctc gtt tcc tgg gac atc cct ggg gct aga gca ctg 96 Arg Phe Leu Ala Leu Val Ser Trp Asp Ile Pro Gly Ala Arg Ala Leu 20 25 30 gac aat gga ttg gca agg acg cct acc atg ggc tgg ctg cac tgg gag 144 Asp Asn Gly Leu Ala Arg Thr Pro Thr Met Gly Trp Leu His Trp Glu 35 40 45 cgc ttc atg tgc aac ctt gac tgc cag gaa gag cca gat tcc tgc atc 192 Arg Phe Met Cys Asn Leu Asp Cys Gln Glu Glu Pro Asp Ser Cys Ile 50 55 60 agt gag aag ctc ttc atg gag atg gca gag ctc atg gtc tca gaa ggc 240 Ser Glu Lys Leu Phe Met Glu Met Ala Glu Leu Met Val Ser Glu Gly 65 70 75 80 tgg aag gat gca ggt tat gag tac ctc tgc att gat gac tgt tgg atg 288 Trp Lys Asp Ala Gly Tyr Glu Tyr Leu Cys Ile Asp Asp Cys Trp Met 85 90 95 gct ccc caa aga gat tca gaa ggc aga ctt cag gca gac cct cag cgc 336 Ala Pro Gln Arg Asp Ser Glu Gly Arg Leu Gln Ala Asp Pro Gln Arg 100 105 110 ttt cct cat ggg att cgc cag cta gct aat tat gtt cac agc aaa gga 384 Phe Pro His Gly Ile Arg Gln Leu Ala Asn Tyr Val His Ser Lys Gly 115 120 125 ctg aag cta ggg att tat gca gat gtt gga aat aaa acc tgc gca ggc 432 Leu Lys Leu Gly Ile Tyr Ala Asp Val Gly Asn Lys Thr Cys Ala Gly 130 135 140 ttc cct ggg agt ttt gga tac tac gac att gat gcc cag acc ttt gct 480 Phe Pro Gly Ser Phe Gly Tyr Tyr Asp Ile Asp Ala Gln Thr Phe Ala 145 150 155 160 gac tgg gga gta gat ctg cta aaa ttt gat ggt tgt tac tgt gac agt 528 Asp Trp Gly Val Asp Leu Leu Lys Phe Asp Gly Cys Tyr Cys Asp Ser 165 170 175 ttg gaa aat ttg gca gat ggt tat aag cac atg tcc ttg gcc ctg aat 576 Leu Glu Asn Leu Ala Asp Gly Tyr Lys His Met Ser Leu Ala Leu Asn 180 185 190 agg act ggc aga agc att gtg tac tcc tgt gag tgg cct ctt tat atg 624 Arg Thr Gly Arg Ser Ile Val Tyr Ser Cys Glu Trp Pro Leu Tyr Met 195 200 205 tgg ccc ttt caa aag ccc aat tat aca gaa atc cga cag tac tgc aat 672 Trp Pro Phe Gln Lys Pro Asn Tyr Thr Glu Ile Arg Gln Tyr Cys Asn 210 215 220 cac tgg cga aat ttt gct gac att gat gat tcc tgg aaa agt ata aag 720 His Trp Arg Asn Phe Ala Asp Ile Asp Asp Ser Trp Lys Ser Ile Lys 225 230 235 240 agt atc ttg gac tgg aca tct ttt aac cag gag aga att gtt gat gtt 768 Ser Ile Leu Asp Trp Thr Ser Phe Asn Gln Glu Arg Ile Val Asp Val 245 250 255 gct gga cca ggg ggt tgg aat gac cca gat atg tta gtg att ggc aac 816 Ala Gly Pro Gly Gly Trp Asn Asp Pro Asp Met Leu Val Ile Gly Asn 260 265 270 ttt ggc ctc agc tgg aat cag caa gta act cag atg gcc ctc tgg gct 864 Phe Gly Leu Ser Trp Asn Gln Gln Val Thr Gln Met Ala Leu Trp Ala 275 280 285 atc atg gct gct cct tta ttc atg tct aat gac ctc cga cac atc agc 912 Ile Met Ala Ala Pro Leu Phe Met Ser Asn Asp Leu Arg His Ile Ser 290 295 300 cct caa gcc aaa gct ctc ctt cag gat aag gac gta att gcc atc aat 960 Pro Gln Ala Lys Ala Leu Leu Gln Asp Lys Asp Val Ile Ala Ile Asn 305 310 315 320 cag gac ccc ttg ggc aag caa ggg tac cag ctt aga cag gga gac aac 1008 Gln Asp Pro Leu Gly Lys Gln Gly Tyr Gln Leu Arg Gln Gly Asp Asn 325 330 335 ttt gaa gtg tgg gaa cga cct ctc tca ggc tta gcc tgg gct gta gct 1056 Phe Glu Val Trp Glu Arg Pro Leu Ser Gly Leu Ala Trp Ala Val Ala 340 345 350 atg ata aac cgg cag gag att ggt gga cct cgc tct tat acc atc gca 1104 Met Ile Asn Arg Gln Glu Ile Gly Gly Pro Arg Ser Tyr Thr Ile Ala 355 360 365 gtt gct tcc ctg ggt aaa gga gtg gcc tgt aat cct gcc tgc ttc atc 1152 Val Ala Ser Leu Gly Lys Gly Val Ala Cys Asn Pro Ala Cys Phe Ile 370 375 380 aca cag ctc ctc cct gtg aaa agg aag cta ggg ttc tat gaa tgg act 1200 Thr Gln Leu Leu Pro Val Lys Arg Lys Leu Gly Phe Tyr Glu Trp Thr 385 390 395 400 tca agg tta aga tct gaa aag gac gaa tta tga 1233 Ser Arg Leu Arg Ser Glu Lys Asp Glu Leu * 405 410 22 409 PRT Homo sapiens 22 Gln Leu Arg Asn Pro Glu Leu His Leu Gly Cys Ala Leu Ala Leu Arg 1 5 10 15 Phe Leu Ala Leu Val Ser Trp Asp Ile Pro Gly Ala Arg Ala Leu Asp 20 25 30 Asn Gly Leu Ala Arg Thr Pro Thr Met Gly Trp Leu His Trp Glu Arg 35 40 45 Phe Met Cys Asn Leu Asp Cys Gln Glu Glu Pro Asp Ser Cys Ile Ser 50 55 60 Glu Lys Leu Phe Met Glu Met Ala Glu Leu Met Val Ser Glu Gly Trp 65 70 75 80 Lys Asp Ala Gly Tyr Glu Tyr Leu Cys Ile Asp Asp Cys Trp Met Ala 85 90 95 Pro Gln Arg Asp Ser Glu Gly Arg Leu Gln Ala Asp Pro Gln Arg Phe 100 105 110 Pro His Gly Ile Arg Gln Leu Ala Asn Tyr Val His Ser Lys Gly Leu 115 120 125 Lys Leu Gly Ile Tyr Ala Asp Val Gly Asn Lys Thr Cys Ala Gly Phe 130 135 140 Pro Gly Ser Phe Gly Tyr Tyr Asp Ile Asp Ala Gln Thr Phe Ala Asp 145 150 155 160 Trp Gly Val Asp Leu Leu Lys Phe Asp Gly Cys Tyr Cys Asp Ser Leu 165 170 175 Glu Asn Leu Ala Asp Gly Tyr Lys His Met Ser Leu Ala Leu Asn Arg 180 185 190 Thr Gly Arg Ser Ile Val Tyr Ser Cys Glu Trp Pro Leu Tyr Met Trp 195 200 205 Pro Phe Gln Lys Pro Asn Tyr Thr Glu Ile Arg Gln Tyr Cys Asn His 210 215 220 Trp Arg Asn Phe Ala Asp Ile Asp Asp Ser Trp Lys Ser Ile Lys Ser 225 230 235 240 Ile Leu Asp Trp Thr Ser Phe Asn Gln Glu Arg Ile Val Asp Val Ala 245 250 255 Gly Pro Gly Gly Trp Asn Asp Pro Asp Met Leu Val Ile Gly Asn Phe 260 265 270 Gly Leu Ser Trp Asn Gln Gln Val Thr Gln Met Ala Leu Trp Ala Ile 275 280 285 Met Ala Ala Pro Leu Phe Met Ser Asn Asp Leu Arg His Ile Ser Pro 290 295 300 Gln Ala Lys Ala Leu Leu Gln Asp Lys Asp Val Ile Ala Ile Asn Gln 305 310 315 320 Asp Pro Leu Gly Lys Gln Gly Tyr Gln Leu Arg Gln Gly Asp Asn Phe 325 330 335 Glu Val Trp Glu Arg Pro Leu Ser Gly Leu Ala Trp Ala Val Ala Met 340 345 350 Ile Asn Arg Gln Glu Ile Gly Gly Pro Arg Ser Tyr Thr Ile Ala Val 355 360 365 Ala Ser Leu Gly Lys Gly Val Ala Cys Asn Pro Ala Cys Phe Ile Thr 370 375 380 Gln Leu Leu Pro Val Lys Arg Lys Leu Gly Phe Tyr Glu Trp Thr Ser 385 390 395 400 Arg Leu Arg Ser Glu Lys Asp Glu Leu 405 23 30 PRT Tobacco mosaic virus 23 Thr Ser Arg Leu Arg Ser His Ile Asn Pro Thr Gly Thr Val Leu Leu 1 5 10 15 Gln Leu Glu Asn Thr Met Gln Met Ser Leu Lys Asp Leu Leu 20 25 30 24 36 PRT Tobacco mosaic virus 24 Thr Ser Arg Leu Arg Ser His Ile Asn Pro Thr Gly Thr Val Leu Leu 1 5 10 15 Gln Leu Glu Asn Thr Met Gln Met Ser Leu Lys Asp Leu Leu Ser Glu 20 25 30 Lys Asp Glu Leu 35 25 26 PRT Tobacco mosaic virus 25 Thr Ser Arg Leu Arg Ser His Ile Asn Pro Thr Gly Thr Val Leu Leu 1 5 10 15 Gln Leu Glu Asn Thr Met Gln Met Ser Leu 20 25 26 32 PRT Tobacco mosaic virus 26 Thr Ser Arg Leu Arg Ser His Ile Asn Pro Thr Gly Thr Val Leu Leu 1 5 10 15 Gln Leu Glu Asn Thr Met Gln Met Ser Leu Ser Glu Lys Asp Glu Leu 20 25 30 27 22 PRT Tobacco mosaic virus 27 Thr Ser Arg Leu Arg Ser His Ile Asn Pro Thr Gly Thr Val Leu Leu 1 5 10 15 Gln Leu Glu Asn Thr Met 20 28 29 PRT Tobacco mosaic virus 28 Thr Ser Arg Leu Arg Ser His Ile Asn Pro Thr Gly Thr Thr Val Leu 1 5 10 15 Leu Gln Leu Glu Asn Thr Met Ser Glu Lys Asp Glu Leu 20 25 29 18 PRT Tobacco mosaic virus 29 Thr Ser Arg Leu Arg Ser His Ile Asn Pro Thr Gly Thr Val Leu Leu 1 5 10 15 Gln Leu 30 24 PRT Tobacco mosaic virus 30 Thr Ser Arg Leu Arg Ser His Ile Asn Pro Thr Gly Thr Val Leu Leu 1 5 10 15 Gln Leu Ser Glu Lys Asp Glu Leu 20 31 5 PRT Tobacco mosaic virus 31 Thr Ser Arg Leu Arg 1 5 32 11 PRT Tobacco mosaic virus 32 Thr Ser Arg Leu Arg Ser Glu Lys Asp Glu Leu 1 5 10 33 11641 DNA Tobacco mosaic virus 33 gtatttttac aacaattacc aacaacaaca aacaacaaac aacattacaa ttactattta 60 caattacaat ggcatacaca cagacagcta ccacatcagc tttgctggac actgtccgag 120 gaaacaactc cttggtcaat gatctagcaa agcgtcgtct ttacgacaca gcggttgaag 180 agtttaacgc tcgtgaccgc aggcccaagg tgaacttttc aaaagtaata agcgaggagc 240 agacgcttat tgctacccgg gcgtatccag aattccaaat tacattttat aacacgcaaa 300 atgccgtgca ttcgcttgca ggtggattgc gatctttaga actggaatat ctgatgatgc 360 aaattcccta cggatcattg acttatgaca taggcgggaa ttttgcatcg catctgttca 420 agggacgagc atatgtacac tgctgtatgc ccaacctgga cgttcgagac atcatgcggc 480 acgaaggcca gaaagacagt attgaactat acctttctag gctagagaga ggggggaaaa 540 cagtccccaa cttccaaaag gaagcatttg acagatacgc agaaattcct gaagacgctg 600 tctgtcacaa tactttccag acaatgcgac atcagccgat gcagcaatca ggcagagtgt 660 atgccattgc gctacacagc atatatgaca taccagccga tgagttcggg gcggcactct 720 tgaggaaaaa tgtccatacg tgctatgccg ctttccactt ctctgagaac ctgcttcttg 780 aagattcata cgtcaatttg gacgaaatca acgcgtgttt ttcgcgcgat ggagacaagt 840 tgaccttttc ttttgcatca gagagtactc ttaattattg tcatagttat tctaatattc 900 ttaagtatgt gtgcaaaact tacttcccgg cctctaatag agaggtttac atgaaggagt 960 ttttagtcac cagagttaat acctggtttt gtaagttttc tagaatagat acttttcttt 1020 tgtacaaagg tgtggcccat aaaagtgtag atagtgagca gttttatact gcaatggaag 1080 acgcatggca ttacaaaaag actcttgcaa tgtgcaacag cgagagaatc ctccttgagg 1140 attcatcatc agtcaattac tggtttccca aaatgaggga tatggtcatc gtaccattat 1200 tcgacatttc tttggagact agtaagagga cgcgcaagga agtcttagtg tccaaggatt 1260 tcgtgtttac agtgcttaac cacattcgaa cataccaggc gaaagctctt acatacgcaa 1320 atgttttgtc ctttgtcgaa tcgattcgat cgagggtaat cattaacggt gtgacagcga 1380 ggtccgaatg ggatgtggac aaatctttgt tacaatcctt gtccatgacg ttttacctgc 1440 atactaagct tgccgttcta aaggatgact tactgattag caagtttagt ctcggttcga 1500 aaacggtgtg ccagcatgtg tgggatgaga tttcgctggc gtttgggaac gcatttccct 1560 ccgtgaaaga gaggctcttg aacaggaaac ttatcagagt ggcaggcgac gcattagaga 1620 tcagggtgcc tgatctatat gtgaccttcc acgacagatt agtgactgag tacaaggcct 1680 ctgtggacat gcctgcgctt gacattagga agaagatgga agaaacggaa gtgatgtaca 1740 atgcactttc agagttatcg gtgttaaggg agtctgacaa attcgatgtt gatgtttttt 1800 cccagatgtg ccaatctttg gaagttgacc caatgacggc agcgaaggtt atagtcgcgg 1860 tcatgagcaa tgagagcggt ctgactctca catttgaacg acctactgag gcgaatgttg 1920 cgctagcttt acaggatcaa gagaaggctt cagaaggtgc tttggtagtt acctcaagag 1980 aagttgaaga accgtccatg aagggttcga tggccagagg agagttacaa ttagctggtc 2040 ttgctggaga tcatccggag tcgtcctatt ctaagaacga ggagatagag tctttagagc 2100 agtttcatat ggcaacggca gattcgttaa ttcgtaagca gatgagctcg attgtgtaca 2160 cgggtccgat taaagttcag caaatgaaaa actttatcga tagcctggta gcatcactat 2220 ctgctgcggt gtcgaatctc gtcaagatcc tcaaagatac agctgctatt gaccttgaaa 2280 cccgtcaaaa gtttggagtc ttggatgttg catctaggaa gtggttaatc aaaccaacgg 2340 ccaagagtca tgcatggggt gttgttgaaa cccacgcgag gaagtatcat gtggcgcttt 2400 tggaatatga tgagcagggt gtggtgacat gcgatgattg gagaagagta gctgtcagct 2460 ctgagtctgt tgtttattcc gacatggcga aactcagaac tctgcgcaga ctgcttcgaa 2520 acggagaacc gcatgtcagt agcgcaaagg ttgttcttgt ggacggagtt ccgggctgtg 2580 ggaaaaccaa agaaattctt tccagggtta attttgatga agatctaatt ttagtacctg 2640 ggaagcaagc cgcggaaatg atcagaagac gtgcgaattc ctcagggatt attgtggcca 2700 cgaaggacaa cgttaaaacc gttgattctt tcatgatgaa ttttgggaaa agcacacgct 2760 gtcagttcaa gaggttattc attgatgaag ggttgatgtt gcatactggt tgtgttaatt 2820 ttcttgtggc gatgtcattg tgcgaaattg catatgttta cggagacaca cagcagattc 2880 catacatcaa tagagtttca ggattcccgt accccgccca ttttgccaaa ttggaagttg 2940 acgaggtgga gacacgcaga actactctcc gttgtccagc cgatgtcaca cattatctga 3000 acaggagata tgagggcttt gtcatgagca cttcttcggt taaaaagtct gtttcgcagg 3060 agatggtcgg cggagccgcc gtgatcaatc cgatctcaaa acccttgcat ggcaagatcc 3120 tgacttttac ccaatcggat aaagaagctc tgctttcaag agggtattca gatgttcaca 3180 ctgtgcatga agtgcaaggc gagacatact ctgatgtttc actagttagg ttaaccccta 3240 caccagtctc catcattgca ggagacagcc cacatgtttt ggtcgcattg tcaaggcaca 3300 cctgttcgct caagtactac actgttgtta tggatccttt agttagtatc attagagatc 3360 tagagaaact tagctcgtac ttgttagata tgtataaggt cgatgcagga acacaatagc 3420 aattacagat tgactcggtg ttcaaaggtt ccaatctttt tgttgcagcg ccaaagactg 3480 gtgatatttc tgatatgcag ttttactatg ataagtgtct cccaggcaac agcaccatga 3540 tgaataattt tgatgctgtt accatgaggt tgactgacat ttcattgaat gtcaaagatt 3600 gcatattgga tatgtctaag tctgttgctg cgcctaagga tcaaatcaaa ccactaatac 3660 ctatggtacg aacggcggca gaaatgccac gccagactgg actattggaa aatttagtgg 3720 cgatgattaa aaggaacttt aacgcacccg agttgtctgg catcattgat attgaaaata 3780 ctgcatcttt agttgtagat aagttttttg atagttattt gcttaaagaa aaaagaaaac 3840 caaataaaaa tgtttctttg ttcagtagag agtctctcaa tagatggtta gaaaagcagg 3900 aacaggtaac aataggccag ctcgcagatt ttgattttgt agatttgcca gcagttgatc 3960 agtacagaca catgattaaa gcacaaccca agcaaaaatt ggacacttca atccaaacgg 4020 agtacccggc tttgcagacg attgtgtacc attcaaaaaa gatcaatgca atatttggcc 4080 cgttgtttag tgagcttact aggcaattac tggacagtgt tgattcgagc agatttttgt 4140 ttttcacaag aaagacacca gcgcagattg aggatttctt cggagatctc gacagtcatg 4200 tgccgatgga tgtcttggag ctggatatat caaaatacga caaatctcag aatgaattcc 4260 actgtgcagt agaatacgag atctggcgaa gattgggttt tgaagacttc ttgggagaag 4320 tttggaaaca agggcataga aagaccaccc tcaaggatta taccgcaggt ataaaaactt 4380 gcatctggta tcaaagaaag agcggggacg tcacgacgtt cattggaaac actgtgatca 4440 ttgctgcatg tttggcctcg atgcttccga tggagaaaat aatcaaagga gccttttgcg 4500 gtgacgatag tctgctgtac tttccaaagg gttgtgagtt tccggatgtg caacactccg 4560 cgaatcttat gtggaatttt gaagcaaaac tgtttaaaaa acagtatgga tacttttgcg 4620 gaagatatgt aatacatcac gacagaggat gcattgtgta ttacgatccc ctaaagttga 4680 tctcgaaact tggtgctaaa cacatcaagg attgggaaca cttggaggag ttcagaaggt 4740 ctctttgtga tgttgctgtt tcgttgaaca attgtgcgta ttacacacag ttggacgacg 4800 ctgtatggga ggttcataag accgcccctc caggttcgtt tgtttataaa agtctggtga 4860 agtatttgtc tgataaagtt ctttttagaa gtttgtttat agatggctct agttgttaaa 4920 ggaaaagtga atatcaatga gtttatcgac ctgacaaaaa tggagaagat cttaccgtcg 4980 atgtttaccc ctgtaaagag tgttatgtgt tccaaagttg ataaaataat ggttcatgag 5040 aatgagtcat tgtcagaggt gaaccttctt aaaggagtta agcttattga tagtggatac 5100 gtctgtttag ccggtttggt cgtcacgggc gagtggaact tgcctgacaa ttgcagagga 5160 ggtgtgagcg tgtgtctggt ggacaaaagg atggaaagag ccgacgaggc cactctcgga 5220 tcttactaca cagcagctgc aaagaaaaga tttcagttca aggtcgttcc caattatgct 5280 ataaccaccc aggacgcgat gaaaaacgtc tggcaagttt tagttaatat tagaaatgtg 5340 aagatgtcag cgggtttctg tccgctttct ctggagtttg tgtcggtgtg tattgtttat 5400 agaaataata taaaattagg tttgagagag aagattacaa acgtgagaga cggagggccc 5460 atggaactta cagaagaagt cgttgatgag ttcatggaag atgtccctat gtcgatcagg 5520 cttgcaaagt ttcgatctcg aaccggaaaa aagagtgatg tccgcaaagg gaaaaatagt 5580 agtaatgatc ggtcagtgcc gaacaagaac tatagaaatg ttaaggattt tggaggaatg 5640 agttttaaaa agaataattt aatcgatgat gattcggagg ctactgtcgc cgaatcggat 5700 tcgttttaaa tagatcttac agtatcacta ctccatctca gttcgtgttc ttgtcattaa 5760 tatgcaggtg ctgaacacca tggtgaacaa acacttcttg tccctttcgg tcctcatcgt 5820 cctccttggc ctctcctcca acttgacagc cggcatgctg gacaatggat tggcaaggac 5880 gcctaccatg ggctggctgc actgggagcg cttcatgtgc aaccttgact gccaggaaga 5940 gccagattcc tgcatcagtg agaagctctt catggagatg gcagagctca tggtctcaga 6000 aggctggaag gatgcaggtt atgagtacct ctgcattgat gactgttgga tggctcccca 6060 aagagattca gaaggcagac ttcaggcaga ccctcagcgc tttcctcatg ggattcgcca 6120 gctagctaat tatgttcaca gcaaaggact gaagctaggg atttatgcag atgttggaaa 6180 taaaacctgc gcaggcttcc ctgggagttt tggatactac gacattgatg cccagacctt 6240 tgctgactgg ggagtagatc tgctaaaatt tgatggttgt tactgtgaca gtttggaaaa 6300 tttggcagat ggttataagc acatgtcctt ggccctgaat aggactggca gaagcattgt 6360 gtactcctgt gagtggcctc tttatatgtg gccctttcaa aagcccaatt atacagaaat 6420 ccgacagtac tgcaatcact ggcgaaattt tgctgacatt gatgattcct ggaaaagtat 6480 aaagagtatc ttggactgga catcttttaa ccaggagaga attgttgatg ttgctggacc 6540 agggggttgg aatgacccag atatgttagt gattggcaac tttggcctca gctggaatca 6600 gcaagtaact cagatggccc tctgggctat catggctgct cctttattca tgtctaatga 6660 cctccgacac atcagccctc aagccaaagc tctccttcag gataaggacg taattgccat 6720 caatcaggac cccttgggca agcaagggta ccagcttaga cagggagaca actttgaagt 6780 gtgggaacga cctctctcag gcttagcctg ggctgtagct atgataaacc ggcaggagat 6840 tggtggacct cgctcttata ccatcgcagt tgcttccctg ggtaaaggag tggcctgtaa 6900 tcctgcctgc ttcatcacac agctcctccc tgtgaaaagg aagctagggt tctatgaatg 6960 gacttcaagg ttaagaagtc acataaatcc cacaggcact gttttgcttc agctatctga 7020 aaaggacgaa ttatgaccta ggctcgcaaa gtttcgaacc aaatcctcaa aaagaggtcc 7080 gaaaaataat aataatttag gtaaggggcg ttcaggcgga aggcctaaac caaaaagttt 7140 tgatgaagtt gaaaaagagt ttgataattt gattgaagat gaagccgaga cgtcggtcgc 7200 ggattctgat tcgtattaaa tatgtcttac tcaatcactt ctccatcgca atttgtgttt 7260 ttgtcatctg tatgggctga ccctatagaa ttgttaaacg tttgtacaaa ttcgttaggt 7320 aaccagtttc aaacacagca agcaagaact actgttcaac agcagttcag cgaggtgtgg 7380 aaacctttcc ctcagagcac cgtcagattt cctggcgatg tttataaggt gtacaggtac 7440 aatgcagttt tagatcctct aattactgcg ttgctggggg cttttgatac taggaataga 7500 ataatcgaag tagaaaacca gcagagtccg acaacagctg aaacgttaga tgctacccgc 7560 agggtagacg acgctacggt tgcaattcgg tctgctataa ataatttagt taatgaacta 7620 gtaagaggta ctggactgta caatcagaat acttttgaaa gtatgtctgg gttggtctgg 7680 acctctgcac ctgcatctta aatgcatagg tgctgaaata taaagtttgt gtttctaaaa 7740 cacacgtggt acgtacgata acgtacagtg tttttccctc cacttaaatc gaagggtagt 7800 gtcttggagc gcgcggagta aacatatatg gttcatatat gtccgtaggc acgtaaaaaa 7860 agcgagggat tcgaattccc ccggaacccc cggttggggc ccaggtacca attcttgaag 7920 acgaaagggc ctcgtgatac gcctattttt ataggttaat gtcatgataa taatggtttc 7980 ttagacgtca ggtggcactt ttcggggaaa tgtgcgcgga acccctattt gtttattttt 8040 ctaaatacat tcaaatatgt atccgctcat gagacaataa ccctgataaa tgcttcaata 8100 atattgaaaa aggaagagta tgagtattca acatttccgt gtcgccctta ttcccttttt 8160 tgcggcattt tgccttcctg tttttgctca cccagaaacg ctggtgaaag taaaagatgc 8220 tgaagatcag ttgggtgcac gagtgggtta catcgaactg gatctcaaca gcggtaagat 8280 ccttgagagt tttcgccccg aagaacgttt tccaatgatg agcactttta aagttctgct 8340 atgtggcgcg gtattatccc gtgttgacgc cgggcaagag caactcggtc gccgcataca 8400 ctattctcag aatgacttgg ttgagtactc accagtcaca gaaaagcatc ttacggatgg 8460 catgacagta agagaattat gcagtgctgc cataaccatg agtgataaca ctgcggccaa 8520 cttacttctg acaacgatcg gaggaccgaa ggagctaacc gcttttttgc acaacatggg 8580 ggatcatgta actcgccttg atcgttggga accggagctg aatgaagcca taccaaacga 8640 cgagcgtgac accacgatgc ctgcagcaat ggcaacaacg ttgcgcaaac tattaactgg 8700 cgaactactt actctagctt cccggcaaca attaatagac tggatggagg cggataaagt 8760 tgcaggacca cttctgcgct cggcccttcc ggctggctgg tttattgctg ataaatctgg 8820 agccggtgag cgtgggtctc gcggtatcat tgcagcactg gggccagatg gtaagccctc 8880 ccgtatcgta gttatctaca cgacggggag tcaggcaact atggatgaac gaaatagaca 8940 gatcgctgag ataggtgcct cactgattaa gcattggtaa ctgtcagacc aagtttactc 9000 atatatactt tagattgatt taaaacttca tttttaattt aaaaggatct aggtgaagat 9060 cctttttgat aatctcatga ccaaaatccc ttaacgtgag ttttcgttcc actgagcgtc 9120 agaccccgta gaaaagatca aaggatcttc ttgagatcct ttttttctgc gcgtaatctg 9180 ctgcttgcaa acaaaaaaac caccgctacc agcggtggtt tgtttgccgg atcaagagct 9240 accaactctt tttccgaagg taactggctt cagcagagcg cagataccaa atactgtcct 9300 tctagtgtag ccgtagttag gccaccactt caagaactct gtagcaccgc ctacatacct 9360 cgctctgcta atcctgttac cagtggctgc tgccagtggc gataagtcgt gtcttaccgg 9420 gttggactca agacgatagt taccggataa ggcgcagcgg tcgggctgaa cggggggttc 9480 gtgcacacag cccagcttgg agcgaacgac ctacaccgaa ctgagatacc tacagcgtga 9540 gctatgagaa agcgccacgc ttcccgaagg gagaaaggcg gacaggtatc cggtaagcgg 9600 cagggtcgga acaggagagc gcacgaggga gcttccaggg ggaaacgcct ggtatcttta 9660 tagtcctgtc gggtttcgcc acctctgact tgagcgtcga tttttgtgat gctcgtcagg 9720 ggggcggagc ctatggaaaa acgccagcaa cgcggccttt ttacggttcc tggccttttg 9780 ctggcctttt gctcacatgt tctttcctgc gttatcccct gattctgtgg ataaccgtat 9840 taccgccttt gagtgagctg ataccgctcg ccgcagccga acgaccgagc gcagcgagtc 9900 agtgagcgag gaagcggaag agcgcctgat gcggtatttt ctccttacgc atctgtgcgg 9960 tatttcacac cgcatatggt gcactctcag tacaatctgc tctgatgccg catagttaag 10020 ccagtataca ctccgctatc gctacgtgac tgggtcatgg ctgcgccccg acacccgcca 10080 acacccgctg acgcgccctg acgggcttgt ctgctcccgg catccgctta cagacaagct 10140 gtgaccgtct ccgggagctg catgtgtcag aggttttcac cgtcatcacc gaaacgcgcg 10200 aggcagctgc ggtaaagctc atcagcgtgg tcgtgaagcg attcacagat gtctgcctgt 10260 tcatccgcgt ccagctcgtt gagtttctcc agaagcgtta atgtctggct tctgataaag 10320 cgggccatgt taagggcggt tttttcctgt ttggtcactt gatgcctccg tgtaaggggg 10380 aatttctgtt catgggggta atgataccga tgaaacgaga gaggatgctc acgatacggg 10440 ttactgatga tgaacatgcc cggttactgg aacgttgtga gggtaaacaa ctggcggtat 10500 ggatgcggcg ggaccagaga aaaatcactc agggtcaatg ccagcgcttc gttaatacag 10560 atgtaggtgt tccacagggt agccagcagc atcctgcgat gcagatccgg aacataatgg 10620 tgcagggcgc tgacttccgc gtttccagac tttacgaaac acggaaaccg aagaccattc 10680 atgttgttgc tcaggtcgca gacgttttgc agcagcagtc gcttcacgtt cgctcgcgta 10740 tcggtgattc attctgctaa ccagtaaggc aaccccgcca gcctagccgg gtcctcaacg 10800 acaggagcac gatcatgcgc acccgtggcc aggacccaac gctgcccgag atgcgccgcg 10860 tgcggctgct ggagatggcg gacgcgatgg atatgttctg ccaagggttg gtttgcgcat 10920 tcacagttct ccgcaagaat tgattggctc caattcttgg agtggtgaat ccgttagcga 10980 ggtgccgccg gcttccattc aggtcgaggt ggcccggctc catgcaccgc gacgcaacgc 11040 ggggaggcag acaaggtata gggcggcgcc tacaatccat gccaacccgt tccatgtgct 11100 cgccgaggcg gcataaatcg ccgtgacgat cagcggtcca gtgatcgaag ttaggctggt 11160 aagagccgcg agcgatcctt gaagctgtcc ctgatggtcg tcatctacct gcctggacag 11220 catggcctgc aacgcgggca tcccgatgcc gccggaagcg agaagaatca taatggggaa 11280 ggccatccag cctcgcgtcg cgaacgccag caagacgtag cccagcgcgt cggccgccat 11340 gccggcgata atggcctgct tctcgccgaa acgtttggtg gcgggaccag tgacgaaggc 11400 ttgagcgagg gcgtgcaaga ttccgaatac cgcaagcgac aggccgatca tcgtcgcgct 11460 ccagcgaaag cggtcctcgc cgaaaatgac ccagagcgct gccggcacct gtcctacgag 11520 ttgcatgata aagaagacag tcataagtgc ggcgacgata gtcatgcccc gcgcccaccg 11580 gaaggagctg actgggttga aggctctcaa gggcatcggt cgagatttag gtgacactat 11640 a 11641 34 8234 DNA Tobacco mosaic virus 34 gtatttttac aacaattacc aacaacaaca aacaacagac aacattacaa ttactattta 60 caattacaat ggcatacaca cagacagcta ccacatcagc tttgctggac actgtccgag 120 gaaacaactc cttggtcaat gatctagcaa agcgtcgtct ttacgacaca gcggttgaag 180 agtttaacgc tcgtgaccgc aggcccaagg tgaacttttc aaaagtaata agcgaggagc 240 agacgcttat tgctacccgg gcgtatccag aattccaaat tacattttat aacacgcaaa 300 atgccgtgca ttcgcttgca ggtggattgc gatctttaga actggaatat ctgatgatgc 360 aaattcccta cggatcattg acttatgaca taggcgggaa ttttgcatcg catctgttca 420 agggacgagc atatgtacac tgctgcatgc ccaacctgga cgttcgagac atcatgcggc 480 acgaaggcca gaaagacagt attgaactat acctttctag gctagagaga ggggggaaaa 540 cagtccccaa cttccaaaag gaagcatttg acagatacgc agaaattcct gaagacgctg 600 tctgtcacaa tactttccag acatgcgaac atcagccgat gcagcaatca ggcagagtgt 660 atgccattgc gctacacagc atatatgaca taccagccga tgagttcggg gcggcactct 720 tgaggaaaaa tgtccatacg tgctatgccg ctttccactt ctccgagaac ctgcttcttg 780 aagattcatg cgtcaatttg gacgaaatca acgcgtgttt ttcgcgcgat ggagacaagt 840 tgaccttttc ttttgcatca gagagtactc ttaattactg tcatagttat tctaatattc 900 ttaagtatgt gtgcaaaact tacttcccgg cctctaatag agaggtttac atgaaggagt 960 ttttagtcac cagagttaat acctggtttt gtaagttttc tagaatagat acttttcttt 1020 tgtacaaagg tgtggcccat aaaagtgtag atagtgagca gttttatact gcaatggaag 1080 acgcatggca ttacaaaaag actcttgcaa tgtgcaacag cgagagaatc ctccttgggg 1140 attcatcatc agtcaattac tggtttccca aaatgaggga tatggtcatc gtaccattat 1200 tcgacatttc tttggagact agtaagagga cgcgcaagga agtcttagtg tccaaggatt 1260 tcgtgttcac agtgcttaac cacattcgaa cataccaggc gaaagctctt acatacgcaa 1320 atgttttgtc cttcgtcgaa tcgattcgat cgagggtaat cattaacggt gtgacagcga 1380 ggtccgaatg ggatgtggac aaatctttgt tacaatcctt gtccatgacg ttttacctgc 1440 atactaagct tgccgttcta aaggatgact tactgattag caagtttagt ctcggttcga 1500 aaacggtgtg ccagcatgtg tgggatgaga tttcgctggc gtttgggaac gcatttccct 1560 ccgtgaaaga gaggctcttg aacaggaaac ttatcagagt ggcaggcgac gcattagaga 1620 tcagggtgcc tgatctatat gtgaccttcc acgacagatt agtgactgag tacaaggcct 1680 ctgtggacat gcctgcgctt gacattagga agaagatgga agaaacggaa gtgatgtaca 1740 atgcactttc agaattatcg gtgttaaggg agtctgacaa attcgatgtt gatgtttttt 1800 cccagatgtg ccaatctttg gaagttgacc caatgacggc agcgaaggtt atagtcgcgg 1860 tcatgagcaa tgagagcggt ctgactctca catttgaacg acctactgag gcgaatgttg 1920 cgctagcttt acaggatcaa gagaaggctt cagaaggtgc attggtagtt acctcaagag 1980 aagttgaaga accgtccatg aagggttcga tggccagagg agagttacaa ttagctggtc 2040 ttgctggaga tcatccggaa tcgtcctatt ctaagaacga ggagatagag tctttagagc 2100 agtttcatat ggcgacggca gattcgttaa ttcgtaagca gatgagctcg attgtgtaca 2160 cgggtccgat taaagttcag caaatgaaaa actttatcga tagcctggta gcatcactat 2220 ctgctgcggt gtcgaatctc gtcaagatcc tcaaagatac agctgctatt gaccttgaaa 2280 cccgtcaaaa gtttggagtc ttggatgttg catctaggaa gtggttaatc aaaccaacgg 2340 ccaagagtca tgcatggggt gttgttgaaa cccacgcgag ggagtatcat gtggcgcttt 2400 tggaatatga tgagcagggt gtggtgacat gcgatgattg gagaagagta gctgttagct 2460 ctgagtctgt tgtttattcc gacatggcga aactcagaac tctgcgcaga ctgcttcgaa 2520 acggagaacc gcatgtcagt agcgcaaagg ttgttcttgt ggacggagtt ccgggctgtg 2580 gaaaaaccaa agaaattctt tccagggtta attttgatga agatctaatt ttagtacctg 2640 ggaagcaagc cgcggaaatg atcagaagac gtgcgaattc ctcagggatt attgtggcca 2700 cgaaggacaa cgttaaaacc gttgattctt tcatgatgaa ttttgggaaa agcacacgct 2760 gtcagttcaa gaggttattc attgatgaag ggttgatgtt gcatactggt tgtgttaatt 2820 ttcttgtggc gatgtcattg tgcgaaattg catatgttta cggagacaca cagcagattc 2880 catacatcaa tagagtttca ggattcccgt accccgccca ttttgccaaa ttggaagttg 2940 acgaggtgga gacacgcaga actactctcc gttgtccagc cgatgtcaca cattatctga 3000 acaggagata tgagggcttt gtcatgagca cttcttcggt taaaaagtct gtttcgcagg 3060 agatggtcgg cggagccgcc gtgatcaatc cgatctcaaa acccttgcat ggcaagatcc 3120 tgacttttac ccaatcggat aaagaagctc tgctttcaag agggtattca gatgttcaca 3180 ctgtgcatga agtgcaaggc gagacatact ctgatgtttc actagttagg ttaaccccta 3240 caccggtctc catcattgca ggagacagcc cacatgtttt ggtcgcattg tcaaggcaca 3300 cctgttcgct caagtactac actgttgtta tggatccttt agttagtatc attagagatc 3360 tagagaaact tagctcgtac ttgttagata tgtataaggt cgatgcagga acacaatagc 3420 aattacagat tgactcggtg ttcaaaggtt ccaatctttt tgttgcagcg ccaaagactg 3480 gtgatatttc tgatatgcag ttttactatg ataagtgtct cccaggcaac agcaccatga 3540 tgaataattt tgatgctgtt accatgaggt tgactgacat ttcattgaat gtcaaagatt 3600 gcatattgga tatgtctaag tctgttgctg cacctaagga tcaaatcaaa ccactaatac 3660 ctatggtacg aacggcggca gaaatgccac gccagactgg actattggaa aatttagtgg 3720 cgatgattaa aagaaacttt aacgcacccg agttgtctgg catcattgat attgaaaata 3780 ctgcatcttt ggttgtagat aagttttttg atagttattt gcttaaagaa aaaagaaaac 3840 caaataaaaa tgtttctttg ttcagtagag agtctctcaa tagatggtta gaaaagcagg 3900 aacaggtaac aataggccag ctcgcagatt ttgattttgt ggatttgcca gcagttgatc 3960 agtacagaca catgattaaa gcacaaccca aacaaaagtt ggacacttca atccaaacgg 4020 agtacccggc tttgcagacg attgtgtacc attcaaaaaa gatcaatgca atattcggcc 4080 cgttgtttag tgagcttact aggcaattac tggacagtgt tgattcgagc agatttttgt 4140 ttttcacaag aaagacacca gcgcagattg aggatttctt cggagatctc gacagtcatg 4200 tgccgatgga tgtcttggag ctggatatat caaaatacga caaatctcag aatgaattcc 4260 actgtgcagt agaatacgag atctggcgaa gattgggttt cgaagacttc ttgggagaag 4320 tttggaaaca agggcataga aagaccaccc tcaaggatta taccgcaggt ataaaaactt 4380 gcatctggta tcaaagaaag agcggggacg tcacgacgtt cattggaaac actgtgatca 4440 ttgctgcatg tttggcctcg atgcttccga tggagaaaat aatcaaagga gccttttgcg 4500 gtgacgatag tctgctgtac tttccaaagg gttgtgagtt tccggatgtg caacactccg 4560 cgaatcttat gtggaatttt gaagcaaaac tgtttaaaaa acagtatgga tacttttgcg 4620 gaagatatgt aatacatcac gacagaggat gcattgtgta ttacgatccc ctaaagttga 4680 tctcgaaact tggtgctaaa cacatcaagg attgggaaca cttggaggag ttcagaaggt 4740 ctctttgtga tgttgctgtt tcgttgaaca attgtgcgta ttacacacag ttggacgacg 4800 ctgtatggga ggttcataag accgcccctc caggttcgtt tgtttataaa agtctggtga 4860 agtatttgtc tgataaagtt ctttttagaa gtttgtttat agatggctct agttgttaaa 4920 ggaaaagtga atatcaatga gtttatcgac ctgacaaaaa tggagaagat cttaccgtcg 4980 atgtttaccc ctgtaaagag tgttatgtgt tccaaagttg ataaaataat ggttcatgag 5040 aatgagtcat tgtcaggggt gaaccttctt aaaggagtta agcttattga tagtggatac 5100 gtctgtttag ccggtttggt cgtcacgggc gagtggaact tgcctgacaa ttgcagagga 5160 ggtgtgagcg tgtgtctggt ggacaaaagg atggaaagag ccgacgaggc cattctcgga 5220 tcttactaca cagcagctgc aaagaaaaga tttcagttca aggtcgttcc caattatgct 5280 ataaccaccc aggacgcgat gagaaacgtc tggcaagttt tagttaatat tagaaatgtg 5340 aagatgtcag cgggtttctg tccgctttct ctggagtttg tgtcggtgtg tattgtttat 5400 agaaataata taaaattagg tttgagagag aagattacaa acgtgagaga cggagggccc 5460 atggaactta cagaagaagt cgttgatgag ttcatggaag atgtccctat gtcgatcagg 5520 cttgcaaagt ttcgatctcg aaccggaaaa aagagtgatg tccgcaaagg gaaaaatagt 5580 agtagtgatc ggtcagtgcc gaacaagaac tatagaaatg ttaaggattt tggaggaatg 5640 agttttaaaa agaataattt aatcgatgat gattcggagg ctactgtcgc cgaatcggat 5700 tcgttttaaa tagatcttac agtatcacta ctccatctca gttcgtgttc ttgtcattaa 5760 ttaaaatgca gctgaggaac ccagaactac atctgggctg cgcgcttgcg cttcgcttcc 5820 tggccctcgt ttcctgggac atccctgggg ctagagcact ggacaatgga ttggcaagga 5880 cgcctaccat gggctggctg cactgggagc gcttcatgtg caaccttgac tgccaggaag 5940 agccagattc ctgcatcagt gagaagctct tcatggagat ggcagagctc atggtctcag 6000 aaggctggaa ggatgcaggt tatgagtacc tctgcattga tgactgttgg atggctcccc 6060 aaagagattc agaaggcaga cttcaggcag accctcagcg ctttcctcat gggattcgcc 6120 agctagctaa ttatgttcac agcaaaggac tgaagctagg gatttatgca gatgttggaa 6180 ataaaacctg cgcaggcttc cctgggagtt ttggatacta cgacattgat gcccagacct 6240 ttgctgactg gggagtagat ctgctaaaat ttgatggttg ttactgtgac agtttggaaa 6300 atttggcaga tggttataag cacatgtcct tggccctgaa taggactggc agaagcattg 6360 tgtactcctg tgagtggcct ctttatatgt ggccctttca aaagcccaat tatacagaaa 6420 tccgacagta ctgcaatcac tggcgaaatt ttgctgacat tgatgattcc tggaaaagta 6480 taaagagtat cttggactgg acatctttta accaggagag aattgttgat gttgctggac 6540 cagggggttg gaatgaccca gatatgttag tgattggcaa ctttggcctc agctggaatc 6600 agcaagtaac tcagatggcc ctctgggcta tcatggctgc tcctttattc atgtctaatg 6660 acctccgaca catcagccct caagccaaag ctctccttca ggataaggac gtaattgcca 6720 tcaatcagga ccccttgggc aagcaagggt accagcttag acagggagac aactttgaag 6780 tgtgggaacg acctctctca ggcttagcct gggctgtagc tatgataaac cggcaggaga 6840 ttggtggacc tcgctcttat accatcgcag ttgcttccct gggtaaagga gtggcctgta 6900 atcctgcctg cttcatcaca cagctcctcc ctgtgaaaag gaagctaggg ttctatgaat 6960 ggacttcaag gttaagaagt cacataaatc ccacaggcac tgttttgctt cagctatctg 7020 aaaaggacga attatgacct agggggtagt caagatgcat aataaataac ggattgtgtc 7080 cgtaatcaca cgtggtgcgt acgataacgc atagtgtttt tccctccact taaatcgaag 7140 ggttgtgtct tggatcgcgc gggtcaaatg tatatggttc atatacatcc gcaggcacgt 7200 aataaagcga ggggttcggg tcgaggtcgg ctgtgaaact cgaaaaggtt ccggaaaaca 7260 aaaaagagag tggtaggtaa tagtgttaat aataagaaaa taaataatag tggtaagaaa 7320 ggtttgaaag ttgaggaaat tgaggataat gtaagtgatg acgagtctat cgcgtcatcg 7380 agtacgtttt aatcaatatg ccttatacaa tcaactctcc gagccaattt gtttacttaa 7440 gttccgctta tgcagatcct gtgcagctga tcaatctgtg tacaaatgca ttgggtaacc 7500 agtttcaaac gcaacaagct aggacaacag tccaacagca atttgcggat gcctggaaac 7560 ctgtgcctag tatgacagtg agatttcctg catcggattt ctatgtgtat agatataatt 7620 cgacgcttga tccgttgatc acggcgttat taaatagctt cgatactaga aatagaataa 7680 tagaggttga taatcaaccc gcaccgaata ctactgaaat cgttaacgcg actcagaggg 7740 tagacgatgc gactgtagct ataagggctt caatcaataa tttggctaat gaactggttc 7800 gtggaactgg catgttcaat caagcaagct ttgagactgc tagtggactt gtctggacca 7860 caactccggc tacttagcta ttgttgtgag atttcctaaa ataaagtcac tgaagactta 7920 aaattcaggg tggctgatac caaaatcagc agtggttgtt cgtccactta aatataacga 7980 ttgtcatatc tggatccaac agttaaacca tgtgatggtg tatactgtgg tatggcgtaa 8040 aacaacggaa aagtcgctga agacttaaaa ttcagggtgg ctgataccaa aatcagcagt 8100 ggttgttcgt ccacttaaaa ataacgattg tcatatctgg atccaacagt taaaccatgt 8160 gatggtgtat actgtggtat ggcgtaaaac aacggagagg ttcgaatcct cccctaaccg 8220 cgggtagcgg ccca 8234 35 11 PRT Tobacco mosaic virus Xaa = any amino acid 35 Xaa Xaa Pro Xaa Ile Pro Lys Ser Phe Gly Tyr 1 5 10 36 11 PRT Tobacco mosaic virus 36 Ala Arg Pro Cys Ile Pro Lys Ser Phe Gly Tyr 1 5 10 37 6 PRT Rice 37 Ser Glu Lys Asp Glu Leu 1 5

Claims (10)

We claim:
1. A pharmeceutic composition comprising a polypeptide represented by the amino acid sequence of SEQ ID NO: 18.
2. A pharmeceutical composition as set forth in claim 1, wherein the C-terminus of said polypeptide is the amino acid sequence depicted in SEQ ID NO: 30.
3. A pharmeceutical composition as set forth in claim 1, wherein said polypeptide is expressed in a plant.
4. A pharmeceutical composition as set forth in claim 1, wherein said polypeptide includes plant glycosylations.
5. A pharmaceutical composition as set forth in claim 1, wherein said polypeptide is glycosylated at least at one amino acid position selected from the group consisting of amino acid positions 108, 161, 184, and 337.
6. A pharmeceutical composition as set forth in claim 1, wherein said polypeptide is glycosylated at least at one amino acid position selected from the group consisting of amino acid positions 108, 161, and 184.
7. A pharmeceutical composition as set forth in claim 1, wherein said polypeptide has a plant glycosylation pattern at amino acid positions 108, 161, and 184, wherein an alpha 1, 3 fucose is present on the proximal N-acetylglucosamine (GlcNac).
8. A pharmeceutical composition as set forth in claim 1, wherein said polypeptide has a plant glycosylation pattern at amino acid positions 108, 161, and 184, wherein an beta 1, 2 xylose is present on a beta-linked mannose of the core.
9. A pharmeceutical composition as set forth in claim 1, wherein said polypeptide is for usage in enzyme replacement therapy.
10. A pharmaceutical composition as set forth in claim 9, wherein said polypeptide is for treatment of Fabry disease.
US10/851,388 2000-07-26 2004-05-21 Production of lysosomal enzymes in plants by transient expression Abandoned US20040234516A1 (en)

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US09/626,127 US6846968B1 (en) 1988-02-26 2000-07-26 Production of lysosomal enzymes in plants by transient expression
US09/993,059 US6887696B2 (en) 2000-07-26 2001-11-13 Production of lysosomal enzymes in plants by transient expression
US10/103,327 US6890748B2 (en) 2000-07-26 2002-03-20 Production of lysosomal enzymes in plants by transient expression
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US09/626,127 Expired - Fee Related US6846968B1 (en) 1988-02-26 2000-07-26 Production of lysosomal enzymes in plants by transient expression
US09/993,059 Expired - Fee Related US6887696B2 (en) 1988-02-26 2001-11-13 Production of lysosomal enzymes in plants by transient expression
US10/103,327 Expired - Fee Related US6890748B2 (en) 2000-07-26 2002-03-20 Production of lysosomal enzymes in plants by transient expression
US10/602,219 Abandoned US20040016021A1 (en) 1988-02-26 2003-06-23 Production of lysosomal enzymes in plants by transient expression
US10/602,220 Abandoned US20040023281A1 (en) 1988-02-26 2003-06-23 Production of lysosomal enzymes in plants by transient expression
US10/851,388 Abandoned US20040234516A1 (en) 2000-07-26 2004-05-21 Production of lysosomal enzymes in plants by transient expression
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US09/626,127 Expired - Fee Related US6846968B1 (en) 1988-02-26 2000-07-26 Production of lysosomal enzymes in plants by transient expression
US09/993,059 Expired - Fee Related US6887696B2 (en) 1988-02-26 2001-11-13 Production of lysosomal enzymes in plants by transient expression
US10/103,327 Expired - Fee Related US6890748B2 (en) 2000-07-26 2002-03-20 Production of lysosomal enzymes in plants by transient expression
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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11103596B2 (en) 2015-05-11 2021-08-31 Ucl Business Plc Fabry disease gene therapy

Families Citing this family (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IL155588A0 (en) * 2003-04-27 2003-11-23 Metabogal Ltd Methods for expression of enzymatically active recombinant lysosomal enzymes in transgenic plant root cells and vectors used thereby
US20050032211A1 (en) * 1996-09-26 2005-02-10 Metabogal Ltd. Cell/tissue culturing device, system and method
US6906172B2 (en) 1998-03-10 2005-06-14 Large Scale Biology Corporation Flexible processing apparatus for isolating and purifying viruses, soluble proteins and peptides from plant sources
US20030100945A1 (en) 2001-11-23 2003-05-29 Mindguard Ltd. Implantable intraluminal device and method of using same in treating aneurysms
ITRM20020115A1 (en) * 2002-03-01 2003-09-01 Plantechno S R L EXPRESSION OF LYSOSOMIAL ENZYMES IN SEED.
US7951557B2 (en) 2003-04-27 2011-05-31 Protalix Ltd. Human lysosomal proteins from plant cell culture
US20100196345A1 (en) * 2003-04-27 2010-08-05 Protalix Production of high mannose proteins in plant culture
AU2007201909C1 (en) * 2003-04-27 2011-12-01 Protalix Ltd. Production of High Mannose Proteins in Plant Culture
CN1922306B (en) * 2004-02-20 2010-10-06 美国弗劳恩霍夫股份有限公司 Systems and methods for clonal expression in plants
US7935336B2 (en) 2005-11-18 2011-05-03 Tokyo Metropolitan Organization For Medical Research Highly functional enzyme having α-galactosidase activity
US20080248512A1 (en) * 2006-09-12 2008-10-09 Genzyme Corporation Methods for detection of lysosomal storage disease
SI2150608T1 (en) * 2007-05-07 2018-04-30 Protalix Ltd. Large scale disposable bioreactor
JP5507242B2 (en) 2007-05-18 2014-05-28 公益財団法人東京都医学総合研究所 Pharmaceutical composition for enzyme replacement therapy
WO2009024977A2 (en) * 2007-08-20 2009-02-26 Protalix Ltd. Saccharide-containing protein conjugates and uses thereof
US9194011B2 (en) 2009-11-17 2015-11-24 Protalix Ltd. Stabilized alpha-galactosidase and uses thereof
DK3272861T3 (en) 2011-01-20 2020-03-23 Protalix Ltd ALPHA-galactosidase-FORMATIONS
TWI620816B (en) * 2011-03-23 2018-04-11 苜蓿股份有限公司 Method of recovering plant-derived proteins
US20130347144A1 (en) * 2012-04-10 2013-12-26 Prairie Plant Systems Inc. Promoters and methods for transforming tubers and transformed tubers
JP6517692B2 (en) * 2012-09-19 2019-05-22 ジェムバックス アンド カエル カンパニー，リミティド Cell penetrating peptide, conjugate containing the same, and composition containing the same
WO2015013116A1 (en) * 2013-07-25 2015-01-29 Merck Sharp & Dohme Corp. Method for reducing the extent of o-mannosylation of glycoproteins
US20180185495A1 (en) * 2014-11-10 2018-07-05 Alexion Pharmaceuticals, Inc. Therapeutic compositions of alpha-l-iduronidase, iduronate-2-sulfatase, and alpha-galactosidase a and methods of use thereof
JP6936150B2 (en) 2015-03-17 2021-09-15 エレヴァ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングｅｌｅｖａ ＧｍｂＨ Glycosylated lysosomal protein, its production method and use
US20210348204A1 (en) * 2018-10-16 2021-11-11 Trait Biosciences, Inc. Systems, Methods, And Compositions For The Production of Water-Soluble Terpenes Derived From Cannabis Plants

Citations (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4921902A (en) * 1984-02-02 1990-05-01 The Dow Chemical Company Hydrophobie associative composition containing a polymer of a water-soluble monomer and an amphiphilic monomer
US4956282A (en) * 1985-07-29 1990-09-11 Calgene, Inc. Mammalian peptide expression in plant cells
US5082778A (en) * 1986-06-03 1992-01-21 Unilever Patent Holdings B.V. Production of guar alpha-galactosidase by hosts transformed with recombinant dna. methods
US5179023A (en) * 1989-03-24 1993-01-12 Research Corporation Technologies, Inc. Recombinant α-galactosidase a therapy for Fabry disease
US5316931A (en) * 1988-02-26 1994-05-31 Biosource Genetics Corp. Plant viral vectors having heterologous subgenomic promoters for systemic expression of foreign genes
US5356804A (en) * 1990-10-24 1994-10-18 Mount Sinai School Of Medicine Of The City Of New York Cloning and expression of biologically active human α-galactosidase A
US5401650A (en) * 1990-10-24 1995-03-28 The Mount Sinai School Of Medicine Of The City University Of New York Cloning and expression of biologically active α-galactosidase A
US5500365A (en) * 1989-02-24 1996-03-19 Monsanto Company Synthetic plant genes
US5597945A (en) * 1986-07-25 1997-01-28 Board Of Supervisors Of Louisiana State University And Agricultural And Mechanical College Plants genetically enhanced for disease resistance
US5618699A (en) * 1992-03-31 1997-04-08 Kanebo Limited Plant virus vector, plasmid, process for expression of foreign gene and process for obtaining foreign gene product
US5929304A (en) * 1995-09-14 1999-07-27 Croptech Development Corporation Production of lysosomal enzymes in plant-based expression systems
US5955647A (en) * 1994-02-03 1999-09-21 The Scripps Research Institute Method for using tobacco mosaic virus to overproduce peptides and proteins
US5977438A (en) * 1988-02-26 1999-11-02 Biosource Technologies, Inc. Production of peptides in plants as viral coat protein fusions
US6033895A (en) * 1998-03-10 2000-03-07 Biosource Technologies, Inc. Process for isolating and purifying viruses, soluble proteins and peptides from plant sources
US6042832A (en) * 1996-08-28 2000-03-28 Thomas Jefferson University Polypeptides fused with alfalfa mosaic virus or ilarvirus capsid proteins
US6210666B1 (en) * 1997-10-21 2001-04-03 Orphan Medical, Inc. Truncated α-galactosidase A to treat fabry disease
US6232099B1 (en) * 1994-10-18 2001-05-15 Scottish Crop Research Institute Method of producing a chimeric protein

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB8421282D0 (en) 1984-08-22 1984-09-26 Connaught Lab Multispecific antigenic proteins
FR2578671B1 (en) 1985-03-05 1987-05-15 Thomson Csf CONTROL CIRCUIT FOR AN ALTERNATIVE PLASMA PANEL
GB9108386D0 (en) 1991-04-19 1991-06-05 Agricultural Genetics Co Modified plant viruses as vectors
GB9414118D0 (en) 1994-07-13 1994-08-31 Axis Genetics Ltd Modified plant viruses as vectors of heterologous peptides
US5622822A (en) 1994-09-13 1997-04-22 Johnson & Johnson Clinical Diagnostics, Inc. Methods for capture and selective release of nucleic acids using polyethyleneimine and an anionic phosphate ester surfactant and amplification of same
WO1997010359A1 (en) 1995-09-13 1997-03-20 Wakunaga Seiyaku Kabushiki Kaisha Method for concentrating variant nucleic acid and nucleic acid concentration test kit for effecting the method
GB9607899D0 (en) 1996-04-17 1996-06-19 Scottish Crop Research Inst Virus-like particle
WO1997049425A1 (en) 1996-06-25 1997-12-31 Stichting Instituut Voor Dierhouderij En Diergezondheid Vaccine comprising antigens bound to carriers through labile bonds

Patent Citations (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4921902A (en) * 1984-02-02 1990-05-01 The Dow Chemical Company Hydrophobie associative composition containing a polymer of a water-soluble monomer and an amphiphilic monomer
US4956282A (en) * 1985-07-29 1990-09-11 Calgene, Inc. Mammalian peptide expression in plant cells
US5082778A (en) * 1986-06-03 1992-01-21 Unilever Patent Holdings B.V. Production of guar alpha-galactosidase by hosts transformed with recombinant dna. methods
US5597945A (en) * 1986-07-25 1997-01-28 Board Of Supervisors Of Louisiana State University And Agricultural And Mechanical College Plants genetically enhanced for disease resistance
US5589367A (en) * 1988-02-26 1996-12-31 Biosource Technologies, Inc. Recombinant plant viral nucleic acids
US5316931A (en) * 1988-02-26 1994-05-31 Biosource Genetics Corp. Plant viral vectors having heterologous subgenomic promoters for systemic expression of foreign genes
US5977438A (en) * 1988-02-26 1999-11-02 Biosource Technologies, Inc. Production of peptides in plants as viral coat protein fusions
US5500365A (en) * 1989-02-24 1996-03-19 Monsanto Company Synthetic plant genes
US5179023A (en) * 1989-03-24 1993-01-12 Research Corporation Technologies, Inc. Recombinant α-galactosidase a therapy for Fabry disease
US5580757A (en) * 1990-10-24 1996-12-03 The Mount Sinai School Of Medicine Of The City University Of New York Cloning and expression of biologically active α-galactosidase A as a fusion protein
US5401650A (en) * 1990-10-24 1995-03-28 The Mount Sinai School Of Medicine Of The City University Of New York Cloning and expression of biologically active α-galactosidase A
US5356804A (en) * 1990-10-24 1994-10-18 Mount Sinai School Of Medicine Of The City Of New York Cloning and expression of biologically active human α-galactosidase A
US5618699A (en) * 1992-03-31 1997-04-08 Kanebo Limited Plant virus vector, plasmid, process for expression of foreign gene and process for obtaining foreign gene product
US5955647A (en) * 1994-02-03 1999-09-21 The Scripps Research Institute Method for using tobacco mosaic virus to overproduce peptides and proteins
US6232099B1 (en) * 1994-10-18 2001-05-15 Scottish Crop Research Institute Method of producing a chimeric protein
US5929304A (en) * 1995-09-14 1999-07-27 Croptech Development Corporation Production of lysosomal enzymes in plant-based expression systems
US6042832A (en) * 1996-08-28 2000-03-28 Thomas Jefferson University Polypeptides fused with alfalfa mosaic virus or ilarvirus capsid proteins
US6210666B1 (en) * 1997-10-21 2001-04-03 Orphan Medical, Inc. Truncated α-galactosidase A to treat fabry disease
US6033895A (en) * 1998-03-10 2000-03-07 Biosource Technologies, Inc. Process for isolating and purifying viruses, soluble proteins and peptides from plant sources

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11103596B2 (en) 2015-05-11 2021-08-31 Ucl Business Plc Fabry disease gene therapy

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