WO1994018323A1 - Stable bactericidal/permeability-increasing protein products and pharmaceutical compositions containing the same - Google Patents
Stable bactericidal/permeability-increasing protein products and pharmaceutical compositions containing the same Download PDFInfo
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- WO1994018323A1 WO1994018323A1 PCT/US1994/001235 US9401235W WO9418323A1 WO 1994018323 A1 WO1994018323 A1 WO 1994018323A1 US 9401235 W US9401235 W US 9401235W WO 9418323 A1 WO9418323 A1 WO 9418323A1
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- rbpi
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- bpi
- host cell
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- 239000006152 selective media Substances 0.000 description 1
- 230000036303 septic shock Effects 0.000 description 1
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- 108010048818 seryl-histidine Proteins 0.000 description 1
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- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
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- MFBOGIVSZKQAPD-UHFFFAOYSA-M sodium butyrate Chemical compound [Na+].CCCC([O-])=O MFBOGIVSZKQAPD-UHFFFAOYSA-M 0.000 description 1
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Definitions
- Lipopolysaccharide is a major component of the outer membrane of gram-negative bacteria and consists of serotype-specific O-side-chain polysaccharides linked to a conserved region of core oligosaccharide and lipid A. Raetz, Ann. Rev. Biochem., 59:129-170 (1990). LPS is an important mediator in the pathogenesis of gram-negative septic shock, one of the major causes of death in intensive-care units in the United States. Morrison, et al , Ann. Rev. Med. 38:417- 432 (1987).
- LPS-binding proteins have been identified in various mammalian tissues. Morrison, Microb. Pathoi , 7:389-398 (1989); Roeder, et al . Infect. , lmmun. , 57: 1054-1058 (1989).
- BPI bactericidal/permeability-increasing protein
- Human BPI protein has been isolated from polymorphonuclear neutrophils by acid extraction combined with either ion exchange chromatography [Elsbach, J. Biol. Chem. , 254: 11000 (1979)] or E.
- a proteolytic fragment corresponding to the N-terminal portion of human BPI holoprotein possesses the antibacterial efficacy of the naturally-derived 55 kDa human BPI holoprotein.
- the C-terminal region of the isolated human BPI protein displays only slightly detectable anti- bacterial activity.
- a BPI N-terminal fragment, comprising approximately the first 199 amino acids of the human BPI holoprotein, has been produced by recombinant means as a 23 kD protein. Gazzano- Santoro et al , Infect, lmmun. 60:4754-4761 (1992).
- rBPI protein analogs which comprise a BPI N-terminal fragment wherein a cysteine at amino acid position 132 or 135 is replaced by another amino acid, preferably a non-polar amino acid such as serine or alanine.
- the cysteine residue at position 132 of a polypeptide comprising the first 199 N- terminal residues of BPI is replaced by an alanine residue in a recombinant product designated "rBPI(l-199)ala 132 ".
- cysteine at position 135 of a BPI fragment comprising the first 199 N-terminal BPI residues is replaced by a serine, resulting in a recombinant product designated "rBPI(l-199)ser 135 ".
- rBPI(l-199)ser 135 highly preferred is a recombinant product designated "rBPI(l- 193)ala 132 " which is characterized by decreased heterogeneity in terms of the identity of its carboxy terminal residue.
- a polypeptide is taught which comprises the first 193 amino-terminal residues of BPI and which has a stop codon immediately following the codon for leucine at position 193.
- DNA sequences encoding biologically-active rBPI protein fragment products having from about 176 to about 198 of the N-terminal amino acids of BPI. These DNAs allow for production of BPI products in eukaryotic host cells, such as CHO cells, wherein the products display less heterogeneity in terms of the carboxy terminal residues present.
- Figure 2 represents results of SDS-PAGE analysis of rBPI(l-193) and rBPI(l-
- Figure 3 depicts results of cation exchange HPLC analysis of rBPI(l-199) products.
- Figure 5 represents results of reverse phase HPLC run on rBPI(l-199) products.
- Figure 6 represents results of reverse phase HPLC run on rBPI(l-199)ala 132 products.
- Figure 7 presents results of turbidity studies on pharmaceutical compositions containing rBPI products with and without poloxamer/polysorbate surfactant ingredients at pH 7.0 and 57°C.
- Example 1 relates to an exemplary means by which base substitutions are introduced in the nucleotide sequence encoding an exemplary N-terminal fragment of the BPI protein and to the incorporation of such mutated sequences into plasmid vectors.
- Example 2 addresses the incorporation of vectors of Example 1 into appropriate host cells and further describes the expression of recombinant BPI protein polypeptide products of the invention.
- Example 3 relates to construction of DNAs encoding cysteine replacement analog products of the invention and the use thereof in in vitro transcription/translation procedures.
- Example 4 relates to properties of rBPI product polypeptides of the invention.
- the resulting PCR fragment was digested with Sail, resulting in an approximately 529 bp Sail -blunt fragment which was then used in a three-piece ligation, together with the approximately 209 bp PvwII-Sytll fragment described above and the large fragment resulting from Sail and Sstll digestion of pING4503, to generate pING4519.
- pING4530 Another vector, pING4530, was constructed which contained the alanine-for- cysteine replacement as in pING4519, but which contained the gpt selectable marker (allowing for mycophenolic acid resistance) instead of the DHFR marker carried over from pING4503 to pING4519.
- pING4530 a 1629 bp S ⁇ fl-Dr ⁇ lll restriction fragment was isolated from pING4519. This fragment included all of the rBPI(l-199)ala 132 coding region as well as an additional approximately 895 bp vector sequence at the 3' end of the coding region. This fragment was ligated to the large (approximately 7230 bp) Dralll-Satl vector fragment isolated from pING4513 to generate pING4530.
- the approximately 700 bp PCR amplified DNA was digested with Sail and Ec ⁇ RI and the resulting 270 bp fragment, including approximately the first one-third of the BPI(1-199) coding sequence, was purified.
- This SaH-Ecol fragment was ligated to 2 other fragments: (1) a 420 bp Ec ⁇ RI-Sstll fragment from pING4519, encoding the remainder of BPI( 1-199) wherein alanine replaces cysteine at position 132; and (2) an approximately 8000 bp Sst ⁇ l-Sall vector fragment from pING4502 (a vector essentially similar to pING4503 except that it does not include the 30 bp 5' untranslated sequence and has a gpt marker rather than DHFR), to generate pING4533 which contains a gpt marker.
- the resulting approximately 1360 bp Xhol-BamHl fragment was used in a series of 3-piece ligations to generate the following four vectors, all of which have inserts encoding rBPI(l-193)ala 132 and which have the optimized Kozak translation initiation site at residue -27 of the signal: (1) pING4143 (gpt marker), obtained by ligating a pING4223 4574 bp BamHl-Notl fragment (gpt marker), a pING4223 Notl-Xhol BPI insert-containing fragment of approximately 3019 bp, and the pING4537 Xhol-BamHl fragment; (2) pING4146 (DHFR marker), obtained by ligating a pING4222 approximately 4159 bp BamHl-Notl fragment (DHFR marker), a pING4223 Notl-Xh ⁇ l BPI insert-containing fragment of approximately 3019 bp, and the pING4537 Xhol-BamHl fragment; (3)
- the CHO-Kl cell line is maintained in Ham's F12 medium plus 10% fetal bovine serum (FBS) supplemented with glutamine/penicillin/streptomycin (Irvine Scientific, Irvine, CA).
- FBS fetal bovine serum
- the cells were transfected by electroporation with 40 ⁇ g of pING4533 DNA which was first digested with N ⁇ tl, extracted with phenol-chloroform and ethanol precipitated. Following electroporation, the cells were allowed to recover for 24 hours in non-selective Ham's F12 medium.
- the cells were then incubated for 7 days after which the S-sepharose beads were removed and washed with 0.1 M NaCl in 10 mM Tris buffer (pH7.5). The product was eluted from the beads by addition of 1.0 M NaCl in. Tris buffer and quantitated by ELISA as described above.
- the top-producing transformant designated A153, secreted approximately 3 ⁇ g/ml in this assay and was adapted to growth in Excell 301 serum-free medium (JRH Scientific, Lenexa, KS). The adapted cells were grown in 1.5 L fermenters in Excell 301 medium in the presence of S- sepharose beads. Productivity was assessed at 120-140 hours by C4 HPLC analysis of product eluted from S-sepharose beads (50 ml aliquots). The productivity was 15- 25 ⁇ g/L at these stages of the fermentation.
- Plasmid pING4222 contains DNA encoding the rBPI(l-193)ala 132 analog fused to the A-MuLv promoter, optimized Kozak initiation sequence, human gamma- 1 heavy chain 3' untranslated region, and the mouse DHFR gene for selection of transfected cells in a nucleoside-free medium.
- the cell line, CHO DG44 was maintained in Ham's F12 medium plus 10% FBS with glutamine/penicillin/streptomycin.
- the cells were transfected with linearized pING4222 DNA (40 ⁇ g digested with Pvul. phenol-chloroform extracted, ethanol precipitated) using the calcium phosphate method of Wigler, et al Cell, 11:223 (1977).
- the cells were plated in 96- well plates at approximately 10 4 cells/ well and transfectants were obtained by growth in selective medium consisting of ⁇ MEM medium lacking nucleosides (Irvine Scientific) and supplemented with dialyzed FBS (100 ml serum dialyzed vs 4L cold
- each well contained approximately 2-3 colonies.
- the supernatants from wells of a 96-well plate were analyzed for the presence of rBPI(l-
- Plasmid pING4223 contains DNA encoding rBPI(l-193)ala 132 BPI fused to the A-MuLv promoter, optimized Kozak translation initiation sequence, human gamma- 1 heavy chain 3' untranslated sequences, and the gpt marker for selection of
- the Sp2/O cell line was maintained in DMEM medium supplemented with 10% FBS with glutamine/penicillin/streptomycin.
- the Sp2/0 cells were transfected by electroporation with 40 ⁇ g of pING4223 DNA which had been digested with N ⁇ tl, extracted with phenol-chloroform and ethanol precipitated. Following electroporation, the cells were allowed to recover for 48 hours in non-selective
- Clone 2X3 was next transfected by electroporation with pING4221, which contains the his gene for selection of transfectants. Following recovery for 48 hours in DMEM plus 10% FBS medium, the cells were plated in 96-well plates at approximately 10 4 cells/ well in DMEM/FBS supplemented with 6 ⁇ g/ml MPA, 250 ⁇ g/ml xanthine and 8 mM histidinol. Untransfected cells were unable to grow in the presence of the histidinol and MPA. At 1.5-2 weeks, transfected cells were observed
- Plasmid pING4143 contains DNA encoding rBPI(l-193)ala 132 fused to the A-MuLv promoter, optimized Kozak translation initiation sequence, and mouse kappa light chain 3' untranslated sequences along with the gpt gene for selection of
- Plasmid pING4144 is similar to pING4143 except that it contains the human cytomegalovirus (hCMV) promoter instead of the A-MuLv promoter.
- hCMV human cytomegalovirus
- CHO-Kl cell line was transfected with pING4144 DNA in the manner described above in Section A. At approximately 2 weeks, supernatants from approximately 200 wells containing single colonies were analyzed for the presence of BPI-reactive protein by ELISA. The top producers were transferred to 24-well plates and rBPI expression determined in 24-well plates containing sodium butyrate. The top producer (clone 174) secreted approximately 3-5 ⁇ g/ml without butyrate and approximately 15-18 ⁇ g/ml in the presence of 5mM butyrate in this assay. This clone, re-designated clone C1771, was deposited with the American Type Culture
- NSO cells were transfected with pING4143 DNA by electroporation. At approximately 3 weeks, colonies consisting of transfected cells were observed in the 96-well plates. Supernatants from wells containing single colonies were analyzed for the presence of BPI-reactive protein by ELISA. The highest producers were transferred to a 24-well plate. Productivity was assessed as extinct 24-well cultures. The highest producers secreted a 15-16 ⁇ g/ml. The highest producers may be retransfected with a vector, such as pING4150, as described above to yield even higher producers.
- a vector such as pING4150
- pIC124 has the rBPI (l-199)-encoding insert oriented such that its 5' end is adjacent to the Sp6 promoter in pG ⁇ Ml .
- the 31 -amino acid signal sequence in the pIC124 insert was then excised by removing the region between two Hindi sites in pIC124 to create pIC127.
- the excised region was replaced with a linker which restored the initiation codon (ATG) and the sequence encoding the first amino acid of BPI.
- GACGCCACCATGGTC SEQ ID NO: 13
- BPI-29 GACCATGGTGGCGTC (SEQ ID NO: 14).
- Those two oligonucleotides were ligated together with the Hincll-Sstll and Sst ⁇ -Hinc ⁇ fragments from pIC124 to form pIC127.
- rBPI(l-199), rBPI(l-199)ser *35 , and BPI(l-199)ala 132 were expressed in vitro from plasmids pIC127, pMLlOl, and pML102 using the TNT SP6 coupled Reticulocyte Lysate System from ProMega (Madison, WL). That system allows in vitro coupled transcription and translation of cloned genes using a eukaryotic translation system. Each coupled transcription/translation was carried out using the manufacturer's protocols with 2 ⁇ g of plasmid DNA in a total volume of 25 ⁇ l, including 35 S-methionine to generate labeled protein. The labeled protein products were added in 5 ⁇ l aliquots to a 20 ⁇ l urea sample buffer and heated at 95°C for 3 minutes. Aliquots (lO ⁇ l) of each sample were run on a 15%
- the S-sepharose was then removed from the medium and washed with 20mM sodium acetate and lOOmM sodium chloride at pH4.0. A second wash was performed with 20mM sodium acetate and 700mM sodium chloride at pH4.0. The purified rBPI products were eluted with 20mM sodium acetate and lOOOmM sodium chloride at pH4.0.
- Cation exchange HPLC using an MA7C column was also employed to measure the dimer content of rBPI products.
- a Bio-Rad MA7C cartridge (4.6 x 30mm, Bio-Rad Catalog No. 125-00556) equilibrated with 40% buffer B (20mM MES, IM NaCl, pH 5.5) at l.Oml/min was used.
- the rBPI(l-199) product was analyzed by diluting a 1 ml sample to 100 ⁇ g/ml and 200 ⁇ l of the diluted sample was injected onto the column.
- the rBPI was eluted with a gradient of 40% to 100% buffer B over 6 minutes.
- Buffer A comprised 20mM MES at pH5.5.
- polyoxypropylene-polyoxyethylene block copolymer and 0.002% polysorbate 80 (a polysorbate surfactant comprising polyoxyethylene sorbitan fatty acid ester).
- polysorbate 80 a polysorbate surfactant comprising polyoxyethylene sorbitan fatty acid ester.
- UV-Vis spectrophotometer (Shimadzu, Desion, CA) equipped with a temperature-controlled cuvette holder attached to a recirculating water bath. Upon equilibrating the cuvette holder at the desired temperature (57°C, 65°C, or 85°C, see below), absorbance at 280 nm was measured to confirm that samples had been diluted to the proper concentration. Following this, the absorbance of samples at the desired temperature (57°C, 65°C, or 85°C, see below).
- rBPI(l-199)ala 132 and rBPI(l-193)ala 132 exhibited greatly improved resistance to unfolding and particle formation relative to wild-type compositions-regardless of whether the surfactant combination was present. Similar results were obtained at pH 5.0 and 65°C, at pH 5.0 and 75°C and at 85°C, respectively.
- ATC CGT GAA TTC CAG CTT CCC AGT TCC CAG ATA AGC ATG GTG CCC AAT 342 lie Arg Glu Phe Gin Leu Pro Ser Ser Gin lie Ser Met Val Pro Asn 60 65 70
- MOLECULE TYPE cDNA
- cDNA SEQUENCE DESCRIPTION: SEQ ID NO:12: GTCGACGCATGCGAGAGAACATGGC 15
Abstract
Description
Claims
Priority Applications (17)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE69426019T DE69426019T2 (en) | 1993-02-02 | 1994-02-02 | STABLE BACTERICIDAL PROTEINS THAT INCREASE PERMEABILITY AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM |
DK03000252T DK1310558T3 (en) | 1993-02-02 | 1994-02-02 | Stable products of the bactericidal / permeability enhancing protein and pharmaceutical compositions containing them |
EP94908704A EP0689592B1 (en) | 1993-02-02 | 1994-02-02 | Stable bactericidal/permeability-increasing protein products and pharmaceutical compositions containing the same |
AU61702/94A AU693089B2 (en) | 1993-02-02 | 1994-02-02 | Stable bactericidal/permeability-increasing protein products and pharmaceutical compositions containing the same |
CA2155004A CA2155004C (en) | 1993-02-02 | 1994-02-02 | Stable bactericidal/permeability-increasing protein products and pharmaceutical compositions containing the same |
NZ262284A NZ262284A (en) | 1993-02-02 | 1994-02-02 | Bactericidal/permeability-increasing protein analogues and their production, coding sequences and compositions thereof |
JP51821094A JP4139867B2 (en) | 1993-02-02 | 1994-02-02 | Stable protein product with improved bactericidal / permeability and pharmaceutical composition comprising the same |
AT94908704T ATE196650T1 (en) | 1993-02-02 | 1994-02-02 | STABLE BACTERICIDAL PROTEINS WHICH INCREASE PERMEABILITY AND PHARMACEUTICAL COMPOSITIONS CONTAINING SAME |
DK94908704T DK0689592T3 (en) | 1993-02-02 | 1994-02-02 | Stable products of the bactericidal / permeability enhancing protein and pharmaceutical compositions containing them |
NO19953033A NO315705B1 (en) | 1993-02-02 | 1995-08-01 | Bactericidal / permeability-increasing protein or fragment thereof, DNA encoding it, autonomously replicating DNA vector, host cell, process for its preparation, hybrid fusion protein, pharmaceutical preparation, polypeptide for medicine |
FI953658A FI112367B (en) | 1993-02-02 | 1995-08-01 | Methods for making a bactericidal / permeability enhancing protein or biologically active fragments thereof, polypeptide analog or Hybrid fusion protein, and DNA sequences, vectors and host cells useful in the methods |
HK98115811A HK1014548A1 (en) | 1993-02-02 | 1998-12-28 | Stable bactericidal/permeability-increasing protein products and pharmaceutical compositions containing the same |
GR20000402074T GR3034492T3 (en) | 1993-02-02 | 2000-09-28 | Stable bactericidal/permeability-increasing protein products and pharmaceutical compositions containing the same |
NO20023224A NO319156B1 (en) | 1993-02-02 | 2002-07-03 | DNA encoding a biologically active fragment of bactericide / permeability-increasing protein, process for its preparation, as well as a pharmaceutical preparation containing it and isolated biologically active fragment of bactericide / permeability-increasing protein. |
FI20031199A FI115633B (en) | 1993-02-02 | 2003-08-26 | DNA encoding a stable bactericidal / permeability enhancing protein fragment, vector, host cell and method for producing these protein fragments |
NO20050998A NO20050998D0 (en) | 1993-02-02 | 2005-02-24 | DNA encoding a biologically active fragment of bactericidal / premeability-increasing protein process for its preparation, as well as a pharmaceutical preparation containing this |
FI20050243A FI20050243A (en) | 1993-02-02 | 2005-03-07 | DNA encoding a stable bactericidal / permeability-increasing protein fragment, vector, host cell and method for producing these protein fragments |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/013,801 US5420019A (en) | 1993-02-02 | 1993-02-02 | Stable bactericidal/permeability-increasing protein muteins |
US08/013,801 | 1993-02-02 |
Publications (1)
Publication Number | Publication Date |
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WO1994018323A1 true WO1994018323A1 (en) | 1994-08-18 |
Family
ID=21761817
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1994/001235 WO1994018323A1 (en) | 1993-02-02 | 1994-02-02 | Stable bactericidal/permeability-increasing protein products and pharmaceutical compositions containing the same |
Country Status (19)
Country | Link |
---|---|
US (6) | US5420019A (en) |
EP (3) | EP1310558B1 (en) |
JP (4) | JP4139867B2 (en) |
KR (1) | KR100361997B1 (en) |
CN (1) | CN1142996C (en) |
AT (3) | ATE230797T1 (en) |
AU (1) | AU693089B2 (en) |
CA (1) | CA2155004C (en) |
DE (3) | DE69434980T2 (en) |
DK (2) | DK1310558T3 (en) |
ES (2) | ES2288199T3 (en) |
FI (2) | FI112367B (en) |
GR (1) | GR3034492T3 (en) |
HK (1) | HK1014548A1 (en) |
NO (3) | NO315705B1 (en) |
NZ (1) | NZ262284A (en) |
PT (2) | PT689592E (en) |
WO (1) | WO1994018323A1 (en) |
ZA (1) | ZA94703B (en) |
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