CA2276252A1 - Method for solubilization and naturation of somatotropins - Google Patents
Method for solubilization and naturation of somatotropins Download PDFInfo
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- CA2276252A1 CA2276252A1 CA002276252A CA2276252A CA2276252A1 CA 2276252 A1 CA2276252 A1 CA 2276252A1 CA 002276252 A CA002276252 A CA 002276252A CA 2276252 A CA2276252 A CA 2276252A CA 2276252 A1 CA2276252 A1 CA 2276252A1
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- glutamate
- somatotropin
- detergent composition
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/575—Hormones
- C07K14/61—Growth hormones [GH] (Somatotropin)
Abstract
A method for the solubilization and/or naturation of a somatotropin involves contacting a somatotropin with a detergent composition and water under conditions effective to obtain a naturated somatotropin, wherein the detergent composition may be a C10, C12, C16 or C18 acyl glutamate, a C10, C14 or C18 alkyl sulfate, an alcohol ethoxy sulfate, lauroyl ethylenediamine-triacetic acid (LEDA), a C10 to C18 linear alkyl benzene sulfonate, diphenyl disulfonate or an acyl amino acid.
Description
METHOD FOR SOLUBILIZATION AND NATURATION
OF SOMATOTROPINS
.
This application claims the benefit of U.S. provisional application Serial No.
60/034,808, filed December 31, 1996.
BACKGROUND OF THE INVENTION
Somatotropins are growth hormones which were originally discovered in pituitary gland extracts of various animals. Recombinant DNA technology has permitted the expression of somatotropins as heterologous proteins from various host cells.
Such o recombinant somatotropins, e.g., somatotropins produced in a microorganism such as E. coli bacteria that has been transformed using recombinant DNA, are typically produced by the host cell in a precipitated, denatured state having reduced or substantially no bioactivity.
The absence of bioactivity is generally attributed to the conformation of the recombinant somatotropin molecule, which lacks the formation of disulfide bonds.
Recombinant ~ 5 somatotropins are believed to be produced by the host cell in substantial ly reduced form (without disulfide linkages) due to the relatively high redox potential of host cells such as the E coli cell. Most recombinant somatotropins, such as bovine (bST) and porcine somatotropin (pST), are packaged in the host cell as inclusion bodies, also referred to as refractile bodies, which are cytoplasmic aggregates containing the recombinant 2o somatotropin and oligomers thereof.
In order to recover the recombinant somatotropin in a bioactive state, the somatotropin, e.g., in the form of inclusion bodies, is preferably but not necessarily isolated from the host cell, after which the somatotropin may be solubilized to form somatotropin 25 monomers, which may then be naturated into a bioactive conformation. The naturated somatotropin may then be further purified to remove impurities such as other somatotropin species, e. g. , oligomers such as dimers, and host cell proteins, for example, by ion exchange to precipitate the impurities (e.g., as described in U.S. Patent No.
5,182,369, which is ' incorporated herein by reference) or other suitable techniques.
WO 98129433 PCTlUS97124287 For example, Bentle et al., U.S. Patent No. 4,652,630, which is incorporated herein by reference, refers to a method for solubilization and maturation of somatotropin protein from inclusion bodies using an aqueous solution of urea to solubilize the inclusion bodies containing the recombinant somatotropin. Bentle et al. reports using urea solutions having concentrations ranging from 2.5 to 7.5 M and a pH between about 9 and 12 for the solubilization step. Once solubilized, the somatotropin protein can be maturated according to the Bentle et al. method at an alkaline pH.
Other methods have used a detergent to solubilize and maturate a somatotropin.
For o example, European Patent Specification publication nos. 229,110 and 263,902 (The Upjohn Co.), which are incorporated herein by reference, disclose a method for converting an insoluble form of somatotropin from a transformed microorganism to the native disulphide bond conformation by solubilizing and oxidizing the sornatotropin in the presence of a detergent. That method uses a detergent of sodium dodecylsulfate (SDS) or a detergent of the formula:
CH3-(CHZ)~-CO-NRl-CHR2-COOH, wherein n is 8 through 20 inclusive; R~ is methyl or ethyl; and R2 is hydrogen, ethyl, methyl, n-propyl or isopropyl. These specifications further disclose a particular method for solubilizing recombinant bST using an aqueous solution of N-lauroyl methyl glycine, which 2o is represented by the formula:
CH3-(CH2),o-CO-NR~-CHR2-COOH, in a sodium borate buffer at 0.1 to 0.5 M and a pH of 8 to 10.5. After solubilization and maturation, European Patent Specification publication nos. 229, I 10 and 263,902 state that the detergent is removed by an anion exchange resin.
Other publications also disclose methods for the solubilization and maturation of recombinant somatotropins using various detergent and non-detergent compounds including U.S. Patent Nos. 4,677,196 and 4,766,224, which also use SDS; U.S. Patent No.
5,023,323, which uses SDS in combination with a chaotropic agent such as urea or guanidine 3o hydrochloride; U.S. Patent No. 5,240,834, which uses sarkosyl (N-lauroyl sarcosine), and U.S. Patent No. 4,975,529, which uses 2-amino-2-methyl-1-propanol. Each of these patents WO 98129433 PCTlUS97124287 are incorporated herein by reference. Although SDS has been reported in several references for use in somatotropin solubilization and naturation methods, it is further acknowledged that SDS binds relatively tightly to the naturated somatotropin, thus making its complete removal from the somatotropin solution difficult.
There is a need in the art for more economical and efficient methods to obtain recombinant somatotropins with high yield and purity. In particular, there is a need for methods for the solubilization and naturation of recombinant somatotropin proteins to obtain the somatotropin molecules in a bioactive state, preferably using a low amount of o detergent that is readily biodegradable. There is a further need for such methods that use a detergent that is easily removed from the natwated somatotropin.
SUMMARY OF THE INVENTION
This invention generally relates to methods for producing biologically active recombinant somatotropins. More particularly, this invention relates to methods for the I S solubilization and naturation of recombinant somatotropins comprising contacting a somatotropin with a detergent composition and water under conditions effective to obtain a naturated somatotropin, wherein the detergent composition comprises a C ~o to C ( 8 acyl glutamate, a C,o, C,4 or C,8 alkyl sulfate, an alcohol ethoxy sulfate, lauroyl ethylenediaminetriacetic acid (LEDA), a C ~ o to C I g linear alkyl benzene sulfonate, diphenyl 2o disulfonate or an acyl amino acid of formula (I) or formula (II):
A
CH3(CH2)mCONH ~COOH
(I) wherein A is CH2CH2C02H, CH2CH2SCH3, CH2C02H, CH2CONH2, CH2CH2CONH2, CH(CH3)2, CH2CH(CH3)2, CH(CH3)CH2CH3, CH2C6H5, CH2C6H40H or 25 CH20H and m is an integer from 8 to 16;
CH3(CH2)mCONH(CH2)"C02H (II) wherein n is an integer from 1 to 5 and m is an integer from 8 to 16.
OF SOMATOTROPINS
.
This application claims the benefit of U.S. provisional application Serial No.
60/034,808, filed December 31, 1996.
BACKGROUND OF THE INVENTION
Somatotropins are growth hormones which were originally discovered in pituitary gland extracts of various animals. Recombinant DNA technology has permitted the expression of somatotropins as heterologous proteins from various host cells.
Such o recombinant somatotropins, e.g., somatotropins produced in a microorganism such as E. coli bacteria that has been transformed using recombinant DNA, are typically produced by the host cell in a precipitated, denatured state having reduced or substantially no bioactivity.
The absence of bioactivity is generally attributed to the conformation of the recombinant somatotropin molecule, which lacks the formation of disulfide bonds.
Recombinant ~ 5 somatotropins are believed to be produced by the host cell in substantial ly reduced form (without disulfide linkages) due to the relatively high redox potential of host cells such as the E coli cell. Most recombinant somatotropins, such as bovine (bST) and porcine somatotropin (pST), are packaged in the host cell as inclusion bodies, also referred to as refractile bodies, which are cytoplasmic aggregates containing the recombinant 2o somatotropin and oligomers thereof.
In order to recover the recombinant somatotropin in a bioactive state, the somatotropin, e.g., in the form of inclusion bodies, is preferably but not necessarily isolated from the host cell, after which the somatotropin may be solubilized to form somatotropin 25 monomers, which may then be naturated into a bioactive conformation. The naturated somatotropin may then be further purified to remove impurities such as other somatotropin species, e. g. , oligomers such as dimers, and host cell proteins, for example, by ion exchange to precipitate the impurities (e.g., as described in U.S. Patent No.
5,182,369, which is ' incorporated herein by reference) or other suitable techniques.
WO 98129433 PCTlUS97124287 For example, Bentle et al., U.S. Patent No. 4,652,630, which is incorporated herein by reference, refers to a method for solubilization and maturation of somatotropin protein from inclusion bodies using an aqueous solution of urea to solubilize the inclusion bodies containing the recombinant somatotropin. Bentle et al. reports using urea solutions having concentrations ranging from 2.5 to 7.5 M and a pH between about 9 and 12 for the solubilization step. Once solubilized, the somatotropin protein can be maturated according to the Bentle et al. method at an alkaline pH.
Other methods have used a detergent to solubilize and maturate a somatotropin.
For o example, European Patent Specification publication nos. 229,110 and 263,902 (The Upjohn Co.), which are incorporated herein by reference, disclose a method for converting an insoluble form of somatotropin from a transformed microorganism to the native disulphide bond conformation by solubilizing and oxidizing the sornatotropin in the presence of a detergent. That method uses a detergent of sodium dodecylsulfate (SDS) or a detergent of the formula:
CH3-(CHZ)~-CO-NRl-CHR2-COOH, wherein n is 8 through 20 inclusive; R~ is methyl or ethyl; and R2 is hydrogen, ethyl, methyl, n-propyl or isopropyl. These specifications further disclose a particular method for solubilizing recombinant bST using an aqueous solution of N-lauroyl methyl glycine, which 2o is represented by the formula:
CH3-(CH2),o-CO-NR~-CHR2-COOH, in a sodium borate buffer at 0.1 to 0.5 M and a pH of 8 to 10.5. After solubilization and maturation, European Patent Specification publication nos. 229, I 10 and 263,902 state that the detergent is removed by an anion exchange resin.
Other publications also disclose methods for the solubilization and maturation of recombinant somatotropins using various detergent and non-detergent compounds including U.S. Patent Nos. 4,677,196 and 4,766,224, which also use SDS; U.S. Patent No.
5,023,323, which uses SDS in combination with a chaotropic agent such as urea or guanidine 3o hydrochloride; U.S. Patent No. 5,240,834, which uses sarkosyl (N-lauroyl sarcosine), and U.S. Patent No. 4,975,529, which uses 2-amino-2-methyl-1-propanol. Each of these patents WO 98129433 PCTlUS97124287 are incorporated herein by reference. Although SDS has been reported in several references for use in somatotropin solubilization and naturation methods, it is further acknowledged that SDS binds relatively tightly to the naturated somatotropin, thus making its complete removal from the somatotropin solution difficult.
There is a need in the art for more economical and efficient methods to obtain recombinant somatotropins with high yield and purity. In particular, there is a need for methods for the solubilization and naturation of recombinant somatotropin proteins to obtain the somatotropin molecules in a bioactive state, preferably using a low amount of o detergent that is readily biodegradable. There is a further need for such methods that use a detergent that is easily removed from the natwated somatotropin.
SUMMARY OF THE INVENTION
This invention generally relates to methods for producing biologically active recombinant somatotropins. More particularly, this invention relates to methods for the I S solubilization and naturation of recombinant somatotropins comprising contacting a somatotropin with a detergent composition and water under conditions effective to obtain a naturated somatotropin, wherein the detergent composition comprises a C ~o to C ( 8 acyl glutamate, a C,o, C,4 or C,8 alkyl sulfate, an alcohol ethoxy sulfate, lauroyl ethylenediaminetriacetic acid (LEDA), a C ~ o to C I g linear alkyl benzene sulfonate, diphenyl 2o disulfonate or an acyl amino acid of formula (I) or formula (II):
A
CH3(CH2)mCONH ~COOH
(I) wherein A is CH2CH2C02H, CH2CH2SCH3, CH2C02H, CH2CONH2, CH2CH2CONH2, CH(CH3)2, CH2CH(CH3)2, CH(CH3)CH2CH3, CH2C6H5, CH2C6H40H or 25 CH20H and m is an integer from 8 to 16;
CH3(CH2)mCONH(CH2)"C02H (II) wherein n is an integer from 1 to 5 and m is an integer from 8 to 16.
In a further preferred embodiment, the invention is dlrecteii to a method for the solubilization and naturation of a recombinant somatotropin using low amounts of biodegradable detergents that are easily removed from the naturated somatotropin by diafiltration, such as a Clo or C~2 acyl glutamate, N-lauroyl sarcosine, N-decylsulfate (NDS) or lauroyl ethylenediamine-triacetic acid (LEDA).
DESCRIPTION OF ILLUSTRATIVE EMBODIMENTS
The present invention is directed to a method for the naturation of a somatotropin comprising the step of contacting a somatotropin with a detergent composition and water under conditions effective to obtain a naturated somatotropin, wherein the detergent composition comprises a C 1 o to C ~ g acyl glutamate, a C l o, C I4 or C 1 g alkyl sulfate, an alcohol ethoxy sulfate, lauroyl ethylenediaminetriacetic acid (LEDA), a C t o to C ~ g linear alkyl benzene sulfonate, diphenyl disulfonate or an acyl amino acid of the formula (I) or (II):
A
CH3(CH2)mCONH ~COOH
(I) wherein A is CH2CH2C02H, CH2CH2SCH3, CH2C02H, CH2CONH2, CH2CH2CONH2, CH(CH3)2, CH2CH(CH3)2, CH(CH3)CH2CH3, CH2C6H5, CH2C6H40H, or CH20H and m is an integer from 8 to 16;
CH3(CH2)rt,CONH(CH2)"C02H (II) wherein n is an integer from 1 to 5 and m is an integer from 8 to 16. The detergent composition can also comprise an N-alkylated derivative of formula (I) or (II).
The invention is further directed to a method for the solubilization and naturation of a somatotropin comprising the steps of contacting a somatotropin with a detergent composition and water under conditions effective to solubilize the somatotropin, and subsequently adjusting the pH of the resulting somatotropin solution to naturate the somatotropin, wherein the detergent composition comprises a C ~ p to C ~ g acyl glutamate, a Clo, C,4orCEg alkyl sulfate, an alcohol ethoxy sulfate, lauro~~a~i~t~a~~ ~i~
(LEDA), a C to to C i 8 linear alkyl benzene sulfonate, diphenyl disulfonate or an acyl amino acid of the formula (I) or (II):
A
CH3(CH2)mCONH COOH
' (I) s wherein A is CH2CH2C02H, CH2CH2SCH3, CH2C02H, CH2CONH2, CH2CH2CONH2, CH(CH3)2, CH2CH(CH3)2, CH(CH3)CH2CH3, CH2C6H5, CH2C6H40H, or CH20H and m is an integer from 8 to 16;
CH3(CH2)n,CONH(CH2)nC02H (II) wherein n is an integer from 1 to 5 and m is an integer from 8 to 16. The detergent composition can also comprise an N-alkylated derivative of formula (I) or (II).
For purposes of the present invention, the following terms should be considered to have the definitions listed below.
The term "somatotropin" includes mammalian somatotropins, such as bovine, porcine, human, ovine, equine, canine and feline somatotropin, and others such as avian somatotropin. Somatotropins, for purposes of this specification, includes somatotropin proteins having naturally-occurring sequences, analogs and homologs of the naturally-occurring protein having somatotropin-like bioactivity, i.e., they bind to somatotropin receptors in the animal with affinity great enough to enhance juvenile growth rate, lactation andlor feed efficiency. Somatotropins also include variants of the naturally-occurring 2s somatotropin that have been lengthened, shortened, substituted and/or fused to another protein, provided that such variants are subject to solubilization and/or naturation according to the inventive process.
DESCRIPTION OF ILLUSTRATIVE EMBODIMENTS
The present invention is directed to a method for the naturation of a somatotropin comprising the step of contacting a somatotropin with a detergent composition and water under conditions effective to obtain a naturated somatotropin, wherein the detergent composition comprises a C 1 o to C ~ g acyl glutamate, a C l o, C I4 or C 1 g alkyl sulfate, an alcohol ethoxy sulfate, lauroyl ethylenediaminetriacetic acid (LEDA), a C t o to C ~ g linear alkyl benzene sulfonate, diphenyl disulfonate or an acyl amino acid of the formula (I) or (II):
A
CH3(CH2)mCONH ~COOH
(I) wherein A is CH2CH2C02H, CH2CH2SCH3, CH2C02H, CH2CONH2, CH2CH2CONH2, CH(CH3)2, CH2CH(CH3)2, CH(CH3)CH2CH3, CH2C6H5, CH2C6H40H, or CH20H and m is an integer from 8 to 16;
CH3(CH2)rt,CONH(CH2)"C02H (II) wherein n is an integer from 1 to 5 and m is an integer from 8 to 16. The detergent composition can also comprise an N-alkylated derivative of formula (I) or (II).
The invention is further directed to a method for the solubilization and naturation of a somatotropin comprising the steps of contacting a somatotropin with a detergent composition and water under conditions effective to solubilize the somatotropin, and subsequently adjusting the pH of the resulting somatotropin solution to naturate the somatotropin, wherein the detergent composition comprises a C ~ p to C ~ g acyl glutamate, a Clo, C,4orCEg alkyl sulfate, an alcohol ethoxy sulfate, lauro~~a~i~t~a~~ ~i~
(LEDA), a C to to C i 8 linear alkyl benzene sulfonate, diphenyl disulfonate or an acyl amino acid of the formula (I) or (II):
A
CH3(CH2)mCONH COOH
' (I) s wherein A is CH2CH2C02H, CH2CH2SCH3, CH2C02H, CH2CONH2, CH2CH2CONH2, CH(CH3)2, CH2CH(CH3)2, CH(CH3)CH2CH3, CH2C6H5, CH2C6H40H, or CH20H and m is an integer from 8 to 16;
CH3(CH2)n,CONH(CH2)nC02H (II) wherein n is an integer from 1 to 5 and m is an integer from 8 to 16. The detergent composition can also comprise an N-alkylated derivative of formula (I) or (II).
For purposes of the present invention, the following terms should be considered to have the definitions listed below.
The term "somatotropin" includes mammalian somatotropins, such as bovine, porcine, human, ovine, equine, canine and feline somatotropin, and others such as avian somatotropin. Somatotropins, for purposes of this specification, includes somatotropin proteins having naturally-occurring sequences, analogs and homologs of the naturally-occurring protein having somatotropin-like bioactivity, i.e., they bind to somatotropin receptors in the animal with affinity great enough to enhance juvenile growth rate, lactation andlor feed efficiency. Somatotropins also include variants of the naturally-occurring 2s somatotropin that have been lengthened, shortened, substituted and/or fused to another protein, provided that such variants are subject to solubilization and/or naturation according to the inventive process.
"Recombinant" proteins, also referred to as heterologous proteins, are proteins which are normally not produced by the host cell. Recombinant DNA technology has permitted the expression of relatively large amounts of heterologous proteins from transformed host cells. For example, expression of recombinant somatotropins from a variety of animals by transformed microorganisms is known. Examples include Goeddel, et al., "Direct Expression in Escherichia coli of a DNA Sequence Coding for Human Growth Hormone," Nature 281:544-48 ( 1979) and Seeburg, et al., "Efficient Bacterial Expression of Bovine and Porcine Growth Hormones," DNA 2:37-45 ( 1983). The production of somatotropins in transformed microorganisms can be achieved by a variety of recombinant genetic plasmids. Examples include those described in United Kingdom Patent Application GB 20732445A; and Schoner et al., "Role of mRNA Translational Efficiency in Bovine Growth Hormone Expression in Escherichia coli," PNAS USA 81:5403-07 (1984).
Analogs of bST are also known, for example, as disclosed in European Patent Application No.
103,395. The production of bST in transformed microorganisms other than E.
coli has been reported by Gray, et al., "Synthesis of Bovine Growth Hormone by Streptomyces lividans,"
Gene 32:21-30 (1984), and in U.S. Patent No. 4,443,539 for yeast.
"Inclusion bodies," also referred to as "refractile bodies," are the cytoplasmic aggregates and oligomers containing the recombinant somatotropin to be recovered.
A "host cell" is a microbial cell such as bacteria, yeast or other suitable cells such as animal and plant cells that has been transformed to express the recombinant somatotropin.
An exemplary host cell is E. col i K 12 (strain W3110/pBGH-1 ) which has been transformed to permit expression of bovine somatotropin.
"Naturation" involves the formation of correct disulfide bonds such that the somatotropin protein is biologically active upon completion of the naturation step or after further purification. "Folding" refers to the return of the overall conformational shape of the protein sufficient to permit proper oxidation. "Oxidation" refers to the formation of the 3o intramolecular disulfide bonds generally required for a biologically active conformation, preferably the~native biologically active conformation.
Analogs of bST are also known, for example, as disclosed in European Patent Application No.
103,395. The production of bST in transformed microorganisms other than E.
coli has been reported by Gray, et al., "Synthesis of Bovine Growth Hormone by Streptomyces lividans,"
Gene 32:21-30 (1984), and in U.S. Patent No. 4,443,539 for yeast.
"Inclusion bodies," also referred to as "refractile bodies," are the cytoplasmic aggregates and oligomers containing the recombinant somatotropin to be recovered.
A "host cell" is a microbial cell such as bacteria, yeast or other suitable cells such as animal and plant cells that has been transformed to express the recombinant somatotropin.
An exemplary host cell is E. col i K 12 (strain W3110/pBGH-1 ) which has been transformed to permit expression of bovine somatotropin.
"Naturation" involves the formation of correct disulfide bonds such that the somatotropin protein is biologically active upon completion of the naturation step or after further purification. "Folding" refers to the return of the overall conformational shape of the protein sufficient to permit proper oxidation. "Oxidation" refers to the formation of the 3o intramolecular disulfide bonds generally required for a biologically active conformation, preferably the~native biologically active conformation.
"Biological activity" means that the subject somatotropin is capable of effecting its intended in vivo physiological response. The biological activity can be determined in the absence of in vivo testing in the particular species by carrying out suitable bioassays. A
suitable bioassay for the somatotropins is the "rat weight gain bioassay." In this bioassay, > 5 the bioactivity of somatotropin preparations are assessed relative to a known preparation (i. e. , extracted native somatotropin) by relating the amount of weight gain of hypophysectomized rats to varying amounts of administered preparation.
The methods for solubilization and naturation of somatotropins according to the invention may be applied to any type of recombinant somatotropin, particularly bovine somatotropin (bST), porcine somatotropin (pST) and human somatotropin (hST).
The transformation, culturing and fermenting of host cells to produce recombinant somatotropin may be performed by conventional methods. The recombinant somatotropin, generally in the form of inclusion bodies, may also be recovered from the host cell culture by conventional techniques that disrupt the cell so as to release the inclusion bodies, and thereupon the inclusion bodies may be collected as a pellet by differential centrifugation.
The detergent composition to be used in the inventive method generally contains a detergent or combination of detergents that promotes the solubilization of somatotropin 2o obtained from the host cell and/or naturates the somatotropin molecules.
More preferably, the detergent used in the inventive methods is also easily removed from the somatotropin solution upon completion of the naturation step. The detergent composition to be used in the inventive methods may comprise one or more compounds selected from a C, o to C, g acyl glutamate, a C ~ o, C, 4 or C ~ g alkyl sulfate, an alcohol ethoxy sulfate, lauroyl ethylenediaminetriacetic acid (LEDA), a C ~ o to C, g linear alkyl benzene sulfonate, diphenyl disulfonate or an acyl amino acid of the formula (I) or (II):
A
CH3(CH2)mCONH ~COOH
{I) wherein A is CHZCH2C02H, CH2CH2SCH3, CH2C02H, CH2CONH2, CH2CH2CONH2, CH(CH3)2, CH2CH(CH3)2, CH(CH3)CH2CH3, CH2C6H5, CH2C6H40H, or CH20H and m is an integer from 8 to 16;
CH3(CH2)mCONH(CH2)nC02H (II) wherein n is an integer from 1 to 5 and m is an integer from 8 to 16. The detergent composition can also comprise an N-alkylated derivative of formula (I) or (II).
1 o In a preferred embodiment, the detergent is a C ~ o to C ~ g acyl glutamate or a salt thereof, and more preferably a C, o, C 12, C, 6 or C, g acyl glutamate or a salt thereof. For example, the acyl radical may be cocoyl, lauroyl, stearoyl or a mixture thereof. In a preferred embodiment, the acyl glutamate is an acyl glutamate salt of triethanolamine, sodium or potassium. More preferably, the acyl glutamate is sodium lauroyl glutamate t5 (available as AMISOFT LS-11 or AMISOFT LS-11(F) from Ajinomoto), sodium cocoyl glutamate (available as AMISOFT CS-11 or AMISOFT CS-i 1(F) from Ajinomoto), TEA
cocoyl glutamate (available as AMISOFT CT-12 or AMISOFT CT-f2S from Ajinomoto), TEA lauroyl glutamate (available as AMISOFT LT-12 from Ajinomoto), sodium hydrogenated tallowyl glutamate (available as AMISOFT HS-11 or AMISOFT HS-11{F) 2o from Aj inomoto), sodium hydrogenated tallowyl glutamate with sodium cocoyl glutamate (available as AMISOFT GS-11 or AMISOFT GS-11 (F) from Ajinomoto), disodium hydrogenated tallowyl glutamate (available as AMISOFT HS-21 from Ajinomoto), potassium cocoyl glutamate (available as AMISOFT CK-11 or AMISOFT CK-11 (F) from Ajinomoto), cocoyl glutamic acid {available as AMISOFT CA from Ajinomoto) or 25 hydrogenated tallowyl glutamic acid (stearoyl glutamic acid) {available as AMISOFT HA
from Aj inomoto). More preferably, the detergent composition comprises an acyl glutamate of sodium lauroyl glutamate, sodium hydrogenated tallowyl glutamate, sodium cocoyl glutamate, disodium cocoyl glutamate or a combination thereof. Most preferably, the detergent composition comprises a Clfl or C,2 acyl glutamate, and in particular, sodium 30 lauroyl glutamate.
_g-The detergent can also be an N-alkylated derivative of formula (I) or (II), such as acyl N-methyl glutamate, acyl N-methyl aspartate or an N-methyl derivative of Sarkosyl or Amilite.
Acyl glutamate can be added to the subject somatotropin mixture, for example, as a powder or in solution form. For example, acyl glutamate can be prepared as a 10% stock solution having a pH of about 6.9-7.0 by adding 0.84 L H20, 61 mL 10% NaOH, and 100 g of acyl glutamate powder. During the solubilization and naturation steps, acyl glutamate is preferably present in the overall mixture at a concentration in the range of about 0.2 to about 5% weight based on the total naturation mixture, and more preferably about 0.3 to about 3%.
The use of acyl glutamates in the detergent composition in the inventive methods provides a number of economical and environmental advantages, as acyl glutamates are ~ 5 generally available at low cost and high purity and are readily biodegradable. The use of certain acyi glutamates also adds to the overall economics of the inventive methods as they are easily separated from the mixture of naturated somatotropin, particularly by diaflltration, thereby reducing equipment and operation costs.
2o Alternatively, the detergent composition used in the inventive methods comprises a C, o, C, 4 or C, g alkyl sulfate, such as NDS; an alcohol ethoxy sulfate, such as C~2H250(CHZCH20)S03Na or Ci2H250(CH2CH20)3S03Na (available from Stepan Co. as SteoITM CS-130, CS-330 or CS-430) or C~4H290{CH2CH20)3S03Na (available from Henkel Corp. as StandapolTM ES-40); LEDA (available from Hampshire Corp. as Hampshire 25 LEDA); a C, o to C, 8 linear alkyl benzene sulfonate, such as a linear dodecylbenzene sulfonate; diphenyl disulfonate or an acyl amino acid of the formula (I) or (II):
A
CH3{CH2)mCONH COOH
(I) wherein A is CH2CH2C02H, CH2CH2SCH3, CH2C02H, CH2CONH2, CH2CH2CONH2, CH(CH3)2, CH2CH(CH3)2, CH(CH3)CH2CH3, CHZC6H~, CH2C6H40H, or CH20H and m is an integer from 8 to 16;
s CH3(CH2)mCONH(CH2)~C02H (II) wherein n is an integer from 1 to s and m is an integer from 8 to I6.
The solubilization and naturation steps may be conducted at the same volume and detergent concentration. Alternatively, the solubilization step may proceed at less than the final naturation volume as solubilization of the subject protein may be facilitated at higher detergent concentrations. The somatotropin solution may then be diluted to obtain the final naturation volume. For example, the somatotropin may be solubilized in a detergent solution having half of the final naturation volume, after which an amount of water or buffer 1 s is added to obtain the full naturation volume.
The pH of the solubilization step is preferably in the range of about 9 to about 13, and more preferably in the range of about 10 to about 12. The pH of the naturation solution is preferably in the range of about 8 to about 12, more preferably about 9 to about 11 and 20 most preferably about 9.5 to about 10.5.
The naturated somatotropin obtained by the inventive methods is preferably obtained in at least about 80% yield, for example, in a yield of about 85% to 95%, wherein the yield is defined as [naturated somatotropin monomer]/[total reduced somatotropin monomer].
2s A catalyst, such as cystine or cysteine, may be optionally added to the somatotropin composition of the naturation step to increase the rate of formation of the disulfide bonds.
The detergent composition used for soiubilization and/or naturation of the somatotropin is preferably removed from the somatotropin solution after the naturation step 3o to avoid interference with downstream purification steps. The detergent composition may be removed by a variety of methods including ion-exchange, dialysis or combinations of those techniques. In a preferred embodiment, the detergent is removed from the naturated somatotropin composition by diafiltration. In a further preferred embodiment, the diafiltration is conducted with a cellulose membrane. Removal of detergents such as C,o and C12 acyl glutamates, N-lauroyl sarcosine, NDS or LEDA by diafiltration is a significant processing advantage as certain detergents are removed from the somatotropin mixture with a significantly lower number of turnover volumes than known processes. When some detergents are removed by diafiltration alone, they may require in excess of 80 volumes of diafiltration buffer. This large volume is a disadvantage in processing because of the size of the diafiltration equipment required. In contrast, Clo and C,2 acyl glutamates, N-lauroyl t o sarcosine, NDS, and LEDA have been found to be easily removed with preferably fewer than 30 turnover volumes. Clo and C12 acyl glutamates are particularly amenable to removal by diafiltration and are more preferably removed in about 10 to 20 turnover volumes.
Precipitation of impurities and purification of the naturated somatotropin ~ 5 composition having the detergent composition substantially removed may be carried out by conventional methods. For example, Storrs et al., U.S. Patent No. 5,182,369 and Bentle et al., U.S. Patent No. 4,652,630, which are incorporated herein by reference, refer to methods for purifying and recovering biologically active somatotropin monomers from solution following the solubiiization and naturation of inclusion bodies of host cells produced by 20 recombinant DNA methodology.
The methods of the present invention are preferably part of an overall technique for producing a somatotropin product that is suitable for parenteral application to target animals.
The following examples are included to demonstrate preferred embodiments of the invention. It should be appreciated by those of skill in the art that the techniques disclosed in the examples which follow represent techniques discovered by the inventors to function well in the practice of the invention, and thus can be considered to constitute preferred 3o modes for its practice. However, those of skill in the art should, in light of the present disclosure, appreciate that many changes can be made in the specific embodiments which are disclosed and still obtain a like or similar result without departing from the spirit and scope of the invention.
EXAMPLES
Four varieties of acyl glutamate and lauroyl ethylenediaminetriacetic acid (LEDA) were tested and shown to be highly efficient at solubilizing bovine somatotropin (bST) inclusion bodies and allowing the correct maturation of the bST molecules (Examples 1-3).
Examples are also provided for the solubilization and maturation of porcine somatotropin (pST) (Examples 3-4).
to Example 1. Solubilization of bST inclusion bodies An aqueous slurry of bST inclusion bodies was assayed and determined to contain 45 g bST/L. The bST used was the N-methionyl derivative of bST otherwise having the native amino acid sequence beginning with phenylalanine. These solubilization experiments were conducted at room temperature, a solution pH of I 1.5 and at 20 g bST/L.
The solubilization was performed at one half of the maturation volume, i.e., if the maturation was to be carried out in a 1 % detergent and at 10 g bST/L, the solubilization was carried out in a 2% detergent and at 20 g bST/L. The volume was doubled after the soIubilization to start the maturation.
2o Water, detergent and NaOH were combined. A sufficient amount of the base was added such that after the inclusion bodies were added and dissolved, the pH
was 11.5, as determined in a preliminary experiment. The mixture of water, detergent and base was stirred as the inclusion bodies were added, after which stirring was continued for 30 minutes.
Example 2. Naturation of bST
The maturation step was also conducted at room temperature. Following the solubilization step, the pH was adjusted to 9.5 by adding HCI, which also served to nearly double the volume. Water was then added to bring the solution to its final volume. Cystine 3o was then added to achieve a final concentration of 1 mM cystine. The mixture was then stirred overnight to complete the maturation process.
Examples i and 2 were conducted for four different acyl glutamate detergent compositions, sodium lauroyl glutamate, sodium hydrogenated tallowyl glutamate with sodium cocoyl glutamate, sodium hydrogenated tallowyl glutamate and disodium cocoyl glutamate, and LEDA as well as a comparative detergent of sodium lauroyl sarcosinate.
Tables 1 and 2 below summarize the naturation efficiencies a various pH
conditions and detergent concentrations.
Table 1. Naturation Efficiencies (%) for Solubilization pH of 11.5 and Naturation pH of 9.5 Detergent Concentrations DETERGENT 0.05 0.10 0.25 0.50 1.00 1.50 2.00 2.50 Sodium lauroyl - - - - - 90 - -glutamate Sodium - - 93 94 75 37 23 hydrogenated -tallowyl glutamate + sodium cocoyl glutamate Sodium - 54 76 95 88 57 25 15 hydrogenated tallowyl glutamate Disodium cocoyl - - - 63 81 88 69 32 glutamate Lauroyl - - - - - - 67 83 ethylenediaminetri acetic acid Sodium fauroyl 28 37 43 89 65 50 45 45 sarcosinate*
*Comparative example Table 2. Naturation Efficiencies (%) at Various Naturation pH Values Refold pH
DETERGENT 8.5 9.5 10.5 11.5 Sodium lauroyl77 90 85 79 glutamate Sodium 84 95 97 82 hydrogenated tallowyl glutamate Disodium cocoyl71 88 88 76 glutamate Lauroyl 68 83 76 69 ethylenediarnine triacetic acid Sodium lauroyl81 89 81 67 sarcosinate*
*Comparative example Example 3. Solubilization and maturation of pST
PST was solubilized at half of the ultimate maturation volume in 3% lauroyl acylglutamate, 20 g/L pST, pH 11 to 11.5 at room temperature. The pST used was that having the native amino acid sequence beginning with phenylalanine and having an additional alanine at the amino terminus. Following solubilization, 15 to 30 min., the pH
1o was adjusted with HCI, diluted with deionized water to final maturation volume, followed by addition of the cystine catalyst. Final maturation conditions were IO g/L pST, 1.5%
acylglutamate, 1 mM cystine, pH 9.5, at room temperature. The maturation was completed within a few hours.
WO 98129433 PCT/iTS97I24287 Example 4. Removal of acyl glutamate detergent from naturated pST
The lauroyl acyl glutamate detergent used in the naturation step was removed by diafiltration prior to pH precipitation to remove impurities. The acylglutamate was adequately removed with 15 to 20 turnover volumes of cold diafiltration buffer of I mM
NaOH in deionized water.
While the methods of this invention have been described in terms of preferred embodiments, it will be apparent to those of skill in the art that variations may be applied to the method described herein without departing from the concept, spirit and scope of the 1 o invention. All such similar substitutes and modifications apparent to those skilled in the art are deemed to be within the spirit, scope and concept of the invention.
suitable bioassay for the somatotropins is the "rat weight gain bioassay." In this bioassay, > 5 the bioactivity of somatotropin preparations are assessed relative to a known preparation (i. e. , extracted native somatotropin) by relating the amount of weight gain of hypophysectomized rats to varying amounts of administered preparation.
The methods for solubilization and naturation of somatotropins according to the invention may be applied to any type of recombinant somatotropin, particularly bovine somatotropin (bST), porcine somatotropin (pST) and human somatotropin (hST).
The transformation, culturing and fermenting of host cells to produce recombinant somatotropin may be performed by conventional methods. The recombinant somatotropin, generally in the form of inclusion bodies, may also be recovered from the host cell culture by conventional techniques that disrupt the cell so as to release the inclusion bodies, and thereupon the inclusion bodies may be collected as a pellet by differential centrifugation.
The detergent composition to be used in the inventive method generally contains a detergent or combination of detergents that promotes the solubilization of somatotropin 2o obtained from the host cell and/or naturates the somatotropin molecules.
More preferably, the detergent used in the inventive methods is also easily removed from the somatotropin solution upon completion of the naturation step. The detergent composition to be used in the inventive methods may comprise one or more compounds selected from a C, o to C, g acyl glutamate, a C ~ o, C, 4 or C ~ g alkyl sulfate, an alcohol ethoxy sulfate, lauroyl ethylenediaminetriacetic acid (LEDA), a C ~ o to C, g linear alkyl benzene sulfonate, diphenyl disulfonate or an acyl amino acid of the formula (I) or (II):
A
CH3(CH2)mCONH ~COOH
{I) wherein A is CHZCH2C02H, CH2CH2SCH3, CH2C02H, CH2CONH2, CH2CH2CONH2, CH(CH3)2, CH2CH(CH3)2, CH(CH3)CH2CH3, CH2C6H5, CH2C6H40H, or CH20H and m is an integer from 8 to 16;
CH3(CH2)mCONH(CH2)nC02H (II) wherein n is an integer from 1 to 5 and m is an integer from 8 to 16. The detergent composition can also comprise an N-alkylated derivative of formula (I) or (II).
1 o In a preferred embodiment, the detergent is a C ~ o to C ~ g acyl glutamate or a salt thereof, and more preferably a C, o, C 12, C, 6 or C, g acyl glutamate or a salt thereof. For example, the acyl radical may be cocoyl, lauroyl, stearoyl or a mixture thereof. In a preferred embodiment, the acyl glutamate is an acyl glutamate salt of triethanolamine, sodium or potassium. More preferably, the acyl glutamate is sodium lauroyl glutamate t5 (available as AMISOFT LS-11 or AMISOFT LS-11(F) from Ajinomoto), sodium cocoyl glutamate (available as AMISOFT CS-11 or AMISOFT CS-i 1(F) from Ajinomoto), TEA
cocoyl glutamate (available as AMISOFT CT-12 or AMISOFT CT-f2S from Ajinomoto), TEA lauroyl glutamate (available as AMISOFT LT-12 from Ajinomoto), sodium hydrogenated tallowyl glutamate (available as AMISOFT HS-11 or AMISOFT HS-11{F) 2o from Aj inomoto), sodium hydrogenated tallowyl glutamate with sodium cocoyl glutamate (available as AMISOFT GS-11 or AMISOFT GS-11 (F) from Ajinomoto), disodium hydrogenated tallowyl glutamate (available as AMISOFT HS-21 from Ajinomoto), potassium cocoyl glutamate (available as AMISOFT CK-11 or AMISOFT CK-11 (F) from Ajinomoto), cocoyl glutamic acid {available as AMISOFT CA from Ajinomoto) or 25 hydrogenated tallowyl glutamic acid (stearoyl glutamic acid) {available as AMISOFT HA
from Aj inomoto). More preferably, the detergent composition comprises an acyl glutamate of sodium lauroyl glutamate, sodium hydrogenated tallowyl glutamate, sodium cocoyl glutamate, disodium cocoyl glutamate or a combination thereof. Most preferably, the detergent composition comprises a Clfl or C,2 acyl glutamate, and in particular, sodium 30 lauroyl glutamate.
_g-The detergent can also be an N-alkylated derivative of formula (I) or (II), such as acyl N-methyl glutamate, acyl N-methyl aspartate or an N-methyl derivative of Sarkosyl or Amilite.
Acyl glutamate can be added to the subject somatotropin mixture, for example, as a powder or in solution form. For example, acyl glutamate can be prepared as a 10% stock solution having a pH of about 6.9-7.0 by adding 0.84 L H20, 61 mL 10% NaOH, and 100 g of acyl glutamate powder. During the solubilization and naturation steps, acyl glutamate is preferably present in the overall mixture at a concentration in the range of about 0.2 to about 5% weight based on the total naturation mixture, and more preferably about 0.3 to about 3%.
The use of acyl glutamates in the detergent composition in the inventive methods provides a number of economical and environmental advantages, as acyl glutamates are ~ 5 generally available at low cost and high purity and are readily biodegradable. The use of certain acyi glutamates also adds to the overall economics of the inventive methods as they are easily separated from the mixture of naturated somatotropin, particularly by diaflltration, thereby reducing equipment and operation costs.
2o Alternatively, the detergent composition used in the inventive methods comprises a C, o, C, 4 or C, g alkyl sulfate, such as NDS; an alcohol ethoxy sulfate, such as C~2H250(CHZCH20)S03Na or Ci2H250(CH2CH20)3S03Na (available from Stepan Co. as SteoITM CS-130, CS-330 or CS-430) or C~4H290{CH2CH20)3S03Na (available from Henkel Corp. as StandapolTM ES-40); LEDA (available from Hampshire Corp. as Hampshire 25 LEDA); a C, o to C, 8 linear alkyl benzene sulfonate, such as a linear dodecylbenzene sulfonate; diphenyl disulfonate or an acyl amino acid of the formula (I) or (II):
A
CH3{CH2)mCONH COOH
(I) wherein A is CH2CH2C02H, CH2CH2SCH3, CH2C02H, CH2CONH2, CH2CH2CONH2, CH(CH3)2, CH2CH(CH3)2, CH(CH3)CH2CH3, CHZC6H~, CH2C6H40H, or CH20H and m is an integer from 8 to 16;
s CH3(CH2)mCONH(CH2)~C02H (II) wherein n is an integer from 1 to s and m is an integer from 8 to I6.
The solubilization and naturation steps may be conducted at the same volume and detergent concentration. Alternatively, the solubilization step may proceed at less than the final naturation volume as solubilization of the subject protein may be facilitated at higher detergent concentrations. The somatotropin solution may then be diluted to obtain the final naturation volume. For example, the somatotropin may be solubilized in a detergent solution having half of the final naturation volume, after which an amount of water or buffer 1 s is added to obtain the full naturation volume.
The pH of the solubilization step is preferably in the range of about 9 to about 13, and more preferably in the range of about 10 to about 12. The pH of the naturation solution is preferably in the range of about 8 to about 12, more preferably about 9 to about 11 and 20 most preferably about 9.5 to about 10.5.
The naturated somatotropin obtained by the inventive methods is preferably obtained in at least about 80% yield, for example, in a yield of about 85% to 95%, wherein the yield is defined as [naturated somatotropin monomer]/[total reduced somatotropin monomer].
2s A catalyst, such as cystine or cysteine, may be optionally added to the somatotropin composition of the naturation step to increase the rate of formation of the disulfide bonds.
The detergent composition used for soiubilization and/or naturation of the somatotropin is preferably removed from the somatotropin solution after the naturation step 3o to avoid interference with downstream purification steps. The detergent composition may be removed by a variety of methods including ion-exchange, dialysis or combinations of those techniques. In a preferred embodiment, the detergent is removed from the naturated somatotropin composition by diafiltration. In a further preferred embodiment, the diafiltration is conducted with a cellulose membrane. Removal of detergents such as C,o and C12 acyl glutamates, N-lauroyl sarcosine, NDS or LEDA by diafiltration is a significant processing advantage as certain detergents are removed from the somatotropin mixture with a significantly lower number of turnover volumes than known processes. When some detergents are removed by diafiltration alone, they may require in excess of 80 volumes of diafiltration buffer. This large volume is a disadvantage in processing because of the size of the diafiltration equipment required. In contrast, Clo and C,2 acyl glutamates, N-lauroyl t o sarcosine, NDS, and LEDA have been found to be easily removed with preferably fewer than 30 turnover volumes. Clo and C12 acyl glutamates are particularly amenable to removal by diafiltration and are more preferably removed in about 10 to 20 turnover volumes.
Precipitation of impurities and purification of the naturated somatotropin ~ 5 composition having the detergent composition substantially removed may be carried out by conventional methods. For example, Storrs et al., U.S. Patent No. 5,182,369 and Bentle et al., U.S. Patent No. 4,652,630, which are incorporated herein by reference, refer to methods for purifying and recovering biologically active somatotropin monomers from solution following the solubiiization and naturation of inclusion bodies of host cells produced by 20 recombinant DNA methodology.
The methods of the present invention are preferably part of an overall technique for producing a somatotropin product that is suitable for parenteral application to target animals.
The following examples are included to demonstrate preferred embodiments of the invention. It should be appreciated by those of skill in the art that the techniques disclosed in the examples which follow represent techniques discovered by the inventors to function well in the practice of the invention, and thus can be considered to constitute preferred 3o modes for its practice. However, those of skill in the art should, in light of the present disclosure, appreciate that many changes can be made in the specific embodiments which are disclosed and still obtain a like or similar result without departing from the spirit and scope of the invention.
EXAMPLES
Four varieties of acyl glutamate and lauroyl ethylenediaminetriacetic acid (LEDA) were tested and shown to be highly efficient at solubilizing bovine somatotropin (bST) inclusion bodies and allowing the correct maturation of the bST molecules (Examples 1-3).
Examples are also provided for the solubilization and maturation of porcine somatotropin (pST) (Examples 3-4).
to Example 1. Solubilization of bST inclusion bodies An aqueous slurry of bST inclusion bodies was assayed and determined to contain 45 g bST/L. The bST used was the N-methionyl derivative of bST otherwise having the native amino acid sequence beginning with phenylalanine. These solubilization experiments were conducted at room temperature, a solution pH of I 1.5 and at 20 g bST/L.
The solubilization was performed at one half of the maturation volume, i.e., if the maturation was to be carried out in a 1 % detergent and at 10 g bST/L, the solubilization was carried out in a 2% detergent and at 20 g bST/L. The volume was doubled after the soIubilization to start the maturation.
2o Water, detergent and NaOH were combined. A sufficient amount of the base was added such that after the inclusion bodies were added and dissolved, the pH
was 11.5, as determined in a preliminary experiment. The mixture of water, detergent and base was stirred as the inclusion bodies were added, after which stirring was continued for 30 minutes.
Example 2. Naturation of bST
The maturation step was also conducted at room temperature. Following the solubilization step, the pH was adjusted to 9.5 by adding HCI, which also served to nearly double the volume. Water was then added to bring the solution to its final volume. Cystine 3o was then added to achieve a final concentration of 1 mM cystine. The mixture was then stirred overnight to complete the maturation process.
Examples i and 2 were conducted for four different acyl glutamate detergent compositions, sodium lauroyl glutamate, sodium hydrogenated tallowyl glutamate with sodium cocoyl glutamate, sodium hydrogenated tallowyl glutamate and disodium cocoyl glutamate, and LEDA as well as a comparative detergent of sodium lauroyl sarcosinate.
Tables 1 and 2 below summarize the naturation efficiencies a various pH
conditions and detergent concentrations.
Table 1. Naturation Efficiencies (%) for Solubilization pH of 11.5 and Naturation pH of 9.5 Detergent Concentrations DETERGENT 0.05 0.10 0.25 0.50 1.00 1.50 2.00 2.50 Sodium lauroyl - - - - - 90 - -glutamate Sodium - - 93 94 75 37 23 hydrogenated -tallowyl glutamate + sodium cocoyl glutamate Sodium - 54 76 95 88 57 25 15 hydrogenated tallowyl glutamate Disodium cocoyl - - - 63 81 88 69 32 glutamate Lauroyl - - - - - - 67 83 ethylenediaminetri acetic acid Sodium fauroyl 28 37 43 89 65 50 45 45 sarcosinate*
*Comparative example Table 2. Naturation Efficiencies (%) at Various Naturation pH Values Refold pH
DETERGENT 8.5 9.5 10.5 11.5 Sodium lauroyl77 90 85 79 glutamate Sodium 84 95 97 82 hydrogenated tallowyl glutamate Disodium cocoyl71 88 88 76 glutamate Lauroyl 68 83 76 69 ethylenediarnine triacetic acid Sodium lauroyl81 89 81 67 sarcosinate*
*Comparative example Example 3. Solubilization and maturation of pST
PST was solubilized at half of the ultimate maturation volume in 3% lauroyl acylglutamate, 20 g/L pST, pH 11 to 11.5 at room temperature. The pST used was that having the native amino acid sequence beginning with phenylalanine and having an additional alanine at the amino terminus. Following solubilization, 15 to 30 min., the pH
1o was adjusted with HCI, diluted with deionized water to final maturation volume, followed by addition of the cystine catalyst. Final maturation conditions were IO g/L pST, 1.5%
acylglutamate, 1 mM cystine, pH 9.5, at room temperature. The maturation was completed within a few hours.
WO 98129433 PCT/iTS97I24287 Example 4. Removal of acyl glutamate detergent from naturated pST
The lauroyl acyl glutamate detergent used in the naturation step was removed by diafiltration prior to pH precipitation to remove impurities. The acylglutamate was adequately removed with 15 to 20 turnover volumes of cold diafiltration buffer of I mM
NaOH in deionized water.
While the methods of this invention have been described in terms of preferred embodiments, it will be apparent to those of skill in the art that variations may be applied to the method described herein without departing from the concept, spirit and scope of the 1 o invention. All such similar substitutes and modifications apparent to those skilled in the art are deemed to be within the spirit, scope and concept of the invention.
Claims (54)
1. A method for the naturation of a somatotropin comprising:
contacting a somatotropin with a detergent composition and water under conditions effective to obtain a naturated somatotropin, wherein the detergent composition comprises a C10, C12, C16 or C18 acyl glutamate, a C10, C14 or C18 alkyl sulfate, an alcohol ethoxy sulfate, lauroyl ethylenediaminetriacetic acid (LEDA), a C10 to C18 linear alkyl benzene sulfonate, diphenyl disulfonate or an acyl amino acid of the formula (I) or (II):
wherein A is CH2CH2CO2H, CH2CH2SCH3, CH2CO2H, CH2CONH2, CH2CH2CONH2, CH(CH3)2, CH2CH(CH3)2, CH(CH3)CH2CH3, CH2C6H5, CH2C6H4OH, or CH2OH and m is an integer from 8 to 16; or CH3(CH2)m,CONH(CH2)n CO2H (II) wherein n is an integer from 1 to 5 and m is an integer from 8 to 16.
contacting a somatotropin with a detergent composition and water under conditions effective to obtain a naturated somatotropin, wherein the detergent composition comprises a C10, C12, C16 or C18 acyl glutamate, a C10, C14 or C18 alkyl sulfate, an alcohol ethoxy sulfate, lauroyl ethylenediaminetriacetic acid (LEDA), a C10 to C18 linear alkyl benzene sulfonate, diphenyl disulfonate or an acyl amino acid of the formula (I) or (II):
wherein A is CH2CH2CO2H, CH2CH2SCH3, CH2CO2H, CH2CONH2, CH2CH2CONH2, CH(CH3)2, CH2CH(CH3)2, CH(CH3)CH2CH3, CH2C6H5, CH2C6H4OH, or CH2OH and m is an integer from 8 to 16; or CH3(CH2)m,CONH(CH2)n CO2H (II) wherein n is an integer from 1 to 5 and m is an integer from 8 to 16.
2. The method of claim 1, wherein the somatotropin is bovine, porcine or human somatotropin.
3. The method of claim 1, wherein the naturated somatotropin yield is at least about 80%.
4. The method of claim 1, wherein the detergent composition comprises a C10, C12, C16 or C18 acyl glutamate.
5. The method of claim 4, wherein the acyl glutamate is a lauroyl glutamate, a cocoyl glutamate, a tallowyl glutamate or a salt thereof.
6. The method of claim 5, wherein the acyl glutamate is sodium lauroyl glutamate, sodium cocoyl glutamate, TEA cocoyl glutamate, TEA lauroyl glutamate, sodium hydrogenated tallowyl glutamate, sodium hydrogenated tallowyl glutamate with sodium cocoyl glutamate, disodium hydrogenated tallowyl glutamate, potassium cocoyl glutamate, cocoyl glutamic acid or hydrogenated tallowyl glutamic acid.
7. The method of claim 6, wherein the acyl glutamate is sodium lauroyl glutamate, sodium hydrogenated tallowyl glutamate, sodium cocoyl glutamate, sodium hydrogenated tallowyl glutamate with sodium cocoyl glutamate, or disodium cocoyl glutamate.
8. The method of claim 1, wherein the detergent composition comprises a C10, C14 or C18 alkyl sulfate.
9. The method of claim 8, wherein the alkyl sulfate is N-decylsulfate.
10. The method of claim 1, wherein the detergent composition comprises an alcohol ethoxy sulfate.
11. The method of claim 10, wherein the alcohol ethoxy sulfate is C12H25O(CH2CH2O)SO3Na, C12H25O(CH2CH2O)3SO3Na or C14H29O(CH2CH2O)3SO3Na.
12. The method of claim 1, wherein the detergent composition comprises lauroyl ethylenediaminetriacetic acid.
13. The method of claim 1, wherein the detergent composition comprises a C10 to C18 linear alkyl benzene sulfonate.
14. The method of claim 13, wherein the detergent composition comprises dodecylbenzene sulfonate.
15. The method of claim 1, wherein the detergent composition comprises diphenyl disulfonate.
16. The method of claim 1, wherein the detergent composition comprises an acyl amino acid of the formula (I) wherein A is CH2CH2CO2H, CH2CH2SCH3 or CH2CO2H.
17. The method of claim 1, wherein the detergent composition comprises an acyl amino acid of the formula (I) wherein A is CH2CONH2, CH2CH2CONH2, CH(CH3)2, CH2CH(CH3)2, CH(CH3)CH2CH3, CH2C6H5, CH2C6H4OH or CH2OH.
18. The method of claim 1, wherein the detergent composition comprises an acyl amino acid of the formula (II).
19. The method of claim 1, wherein the detergent composition comprises a C10 or C12 acyl glutamate and the method further comprises separating the acyl glutamate from the naturated somatotropin by diafiltration.
20. The method of claim 19, wherein the diafiltration uses fewer than 30 turnover volumes to remove substantially all of the acyl glutamate from the somatotropin.
21. The method of claim 1, wherein the detergent composition comprises lauroyl ethylenediaminetriacetic acid and the method further comprises separating the lauroyl ethylenediaminetriacetic acid from the naturated somatotropin by diafiltration.
22. The method of claim 21, wherein the diafiltration uses fewer than 30 turnover volumes to remove substantially all of the lauroyl ethylenediaminetriacetic acid from the somatotropin.
23. The method of claim 1, wherein the conditions include a pH in the range of about 8 to about 12.
24. The method of claim 23, wherein the pH is in the range of about 9.5 to about 10.5.
25. The method of claim 1, wherein the conditions include a detergent concentration in the range of about 0.2 to about 5% by weight.
26. A method for solubilization and naturation of a somatotropin comprising:
contacting a somatotropin with a detergent composition and water under conditions effective to solubilize the somatotropin, and adjusting the pH of the resulting somatotropin solution to naturate the somatotropin, wherein the detergent composition comprises a C10, C12, C16 or C18 acyl glutamate, a C10, C14 or C18 alkyl sulfate, an alcohol ethoxy sulfate, lauroyl ethylenediaminetriacetic acid (LEDA), a C10 to C18 linear alkyl benzene sulfonate, diphenyl disulfonate or an acyl amino acid of the formula (I) or (II):
wherein A is CH2CH2CO2H, CH2CH2SCH3, CH2CO2H, CH2CONH2, CH2CH2CONH2, CH(CH3)2, CH2CH(CH3)2, CH(CH3)CH2CH3, CH2C6H5, CH2C6H4OH, or CH2OH and m is an integer from 8 to 16;
CH3(CH2)mCONH(CH2)n CO2H (II) wherein n is an integer from 1 to 5 and m is an integer from 8 to 16.
contacting a somatotropin with a detergent composition and water under conditions effective to solubilize the somatotropin, and adjusting the pH of the resulting somatotropin solution to naturate the somatotropin, wherein the detergent composition comprises a C10, C12, C16 or C18 acyl glutamate, a C10, C14 or C18 alkyl sulfate, an alcohol ethoxy sulfate, lauroyl ethylenediaminetriacetic acid (LEDA), a C10 to C18 linear alkyl benzene sulfonate, diphenyl disulfonate or an acyl amino acid of the formula (I) or (II):
wherein A is CH2CH2CO2H, CH2CH2SCH3, CH2CO2H, CH2CONH2, CH2CH2CONH2, CH(CH3)2, CH2CH(CH3)2, CH(CH3)CH2CH3, CH2C6H5, CH2C6H4OH, or CH2OH and m is an integer from 8 to 16;
CH3(CH2)mCONH(CH2)n CO2H (II) wherein n is an integer from 1 to 5 and m is an integer from 8 to 16.
27. The method of claim 26, wherein the somatotropin is bovine, porcine or human somatotropin.
28. The method of claim 26, wherein the naturated somatotropin yield is at least about 80%.
29. The method of claim 26, wherein the detergent composition comprises a C10, C12, C16 or C18 acyl glutamate.
30. The method of claim 29, wherein the acyl glutamate is a lauroyl glutamate, a cocoyl glutamate, a tallowyl glutamate or a salt thereof.
31. The method of claim 30, wherein the acyl glutamate is sodium lauroyl glutamate, sodium cocoyl glutamate, TEA cocoyl glutamate, TEA lauroyl glutamate, sodium hydrogenated tallowyl glutamate, sodium hydrogenated tallowyl glutamate with sodium cocoyl glutamate, disodium hydrogenated tallowyl glutamate, potassium cocoyl glutamate, cocoyl glutamic acid or hydrogenated tallowyl glutamic acid.
32. The method of claim 31, wherein the acyl glutamate is sodium lauroyl glutamate, sodium hydrogenated tallowyl glutamate, sodium cocoyl glutamate, sodium hydrogenated tallowyl glutamate with sodium cocoyl glutamate or disodium cocoyl glutamate.
33. The method of claim 26, wherein the detergent composition comprises a C10, C14 or 18 alkyl sulfate.
34. The method of claim 33, wherein the alkyl sulfate is N-decylsulfate.
35. The method of claim 26, wherein the detergent composition comprises an alcohol ethoxy sulfate.
36. The method of claim 35, wherein the alcohol ethoxy sulfate is C12H25O(CH2CH2O)SO3Na, C12H25O(CH2CH2O)3SO3Na Or C14H29O(CH2CH2O)3SO3Na.
37. The method of claim 26, wherein the detergent composition comprises lauroyl ethylenediaminetriacetic acid.
38. The method of claim 26, wherein the detergent composition comprises a C10 to C18 linear alkyl benzene sulfonate.
39. The method of claim 38, wherein the detergent comprises dodecylbenzene sulfate.
40. The method of claim 26, wherein the detergent composition comprises diphenyl disulfonate.
41. The method of claim 26, wherein the detergent composition comprises and acyl amino acid of the formula (I) wherein A is CH2CH2CO2H, CH2CH2SCH3 or CH2CO2H.
42. The method of claim 26, wherein the detergent composition comprises an acyl amino acid of the formula (I) wherein A is CH2CONH2, CH2CH2CONH2, CH(CH3)z, CH2CH(CH3)2, CH(CH3)CH2CH3, CH2C6H5, CH2C6H4OH or CH2OH.
43. The method of claim 26, wherein the detergent composition comprises an acyl amino acid of the formula (II).
44. The method of claim 26, wherein the detergent composition comprises a C10 or C12 acyl glutamate and the method further comprises separating the acyl glutamate from the naturated somatotropin by diafiltration.
45. The method of claim 44, wherein the diafiltration uses fewer than 30 turnover volumes to remove substantially all of the acyl glutamate from the somatotropin.
46. The method of claim 26, wherein the detergent composition comprises lauroyl ethylenediaminetriacetic acid and the method further comprises separating the lauroyl ethylenediaminetriacetic acid from the naturated somatotropin by diafiltration.
47. The method of claim 46, wherein the diafiltration uses fewer than 30 turnover volumes to remove substantially all of the lauroyl ethylenediaminetriacetic acid from the somatotropin.
48. The method of claim 26, wherein the conditions include a pH in the range of about 9 to about 13.
49. The method of claim 26, wherein the conditions include a pH in the range of about 8 to about 12.
50. The method of claim 49, wherein the pH is in the range of about 9.5 to about 10.5.
51. The method of claim 26, wherein the conditions include a detergent concentration in the range of about 0.2 to about 5% by weight.
52. A method for obtaining bioactive somatotropin comprising:
contacting a somatotropin with a detergent composition and water under conditions effective to solubilize the somatotropin, adjusting the pH of the somatotropin solution to naturate the somatotropin, and removing the detergent composition from the naturated somatotropin by diafiltration, wherein the detergent composition comprises a C10 or C12 acyl glutamate, N-lauroyl sarcosine, N-decylsulfate or lauroyl ethylenediaminetriacetic acid.
contacting a somatotropin with a detergent composition and water under conditions effective to solubilize the somatotropin, adjusting the pH of the somatotropin solution to naturate the somatotropin, and removing the detergent composition from the naturated somatotropin by diafiltration, wherein the detergent composition comprises a C10 or C12 acyl glutamate, N-lauroyl sarcosine, N-decylsulfate or lauroyl ethylenediaminetriacetic acid.
53. The method of claim 52, wherein the diafiltration step uses fewer than 30 turnover volumes to remove substantially all of the detergent from the somatotropin.
54. The method of claim 53, wherein the detergent comprises a C12 acyl glutamate and the diafiltration step uses from 10 to 20 turnover volumes to remove substantially all of the detergent from the somatotropin.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US3480896P | 1996-12-31 | 1996-12-31 | |
| US60/034,808 | 1996-12-31 | ||
| PCT/US1997/024287 WO1998029433A2 (en) | 1996-12-31 | 1997-12-31 | Method for solubilization and naturation of somatotropins |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2276252A1 true CA2276252A1 (en) | 1998-07-09 |
Family
ID=21878743
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002276252A Abandoned CA2276252A1 (en) | 1996-12-31 | 1997-12-31 | Method for solubilization and naturation of somatotropins |
Country Status (8)
| Country | Link |
|---|---|
| US (3) | US6034224A (en) |
| EP (1) | EP0948540A2 (en) |
| JP (1) | JP2001509793A (en) |
| KR (1) | KR100487299B1 (en) |
| AU (1) | AU6937098A (en) |
| CA (1) | CA2276252A1 (en) |
| WO (1) | WO1998029433A2 (en) |
| ZA (1) | ZA9711733B (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ZA9711733B (en) * | 1996-12-31 | 1998-07-01 | Monsanto Co | Method for solubilization and naturation of somatotropins |
| US6794159B1 (en) | 1999-04-30 | 2004-09-21 | Pharmacia Corporation | Method of removing n-terminal alanine residues from polypeptides with aeromonas aminopeptidase |
| US6743600B1 (en) | 1999-04-30 | 2004-06-01 | Monsanto Technologies Llc | Method of removing N-terminal alanine residues from polypeptides with Aeromonas aminopeptidase |
| WO2009136568A1 (en) | 2008-05-08 | 2009-11-12 | 味の素株式会社 | Protein reforming method |
| BR102013026129A2 (en) * | 2013-10-10 | 2016-05-24 | Ouro Fino Participações E Empreendimentos S A | process for the production of active recombinant bovine somatotropin and product obtained |
Family Cites Families (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3985722A (en) * | 1973-12-12 | 1976-10-12 | Ajinomoto Co., Inc. | Process for preparing N-higher aliphatic acyl derivatives of amino acids, peptides or proteins |
| US4443539A (en) * | 1980-02-05 | 1984-04-17 | The Upjohn Company | Process for preparing bovine growth hormone |
| CA1224432A (en) * | 1982-08-17 | 1987-07-21 | Gary N. Buell | Dna sequences, recombinant dna molecules and processes for producing bovine growth hormone-like polypeptides in high yield |
| US4518526A (en) * | 1982-12-22 | 1985-05-21 | Genentech, Inc. | Purification and activity assurance of precipitated heterologous proteins |
| US4511503A (en) * | 1982-12-22 | 1985-04-16 | Genentech, Inc. | Purification and activity assurance of precipitated heterologous proteins |
| US4652630A (en) * | 1985-02-22 | 1987-03-24 | Monsanto Company | Method of somatotropin naturation |
| ES8800957A1 (en) * | 1985-02-22 | 1987-12-01 | Monsanto Co | Method of somatotropin solubilization and naturation. |
| GB8508340D0 (en) * | 1985-03-29 | 1985-05-09 | Creighton T E | Production of protein |
| JPH06104070B2 (en) * | 1985-06-26 | 1994-12-21 | ジ・アップジョン・カンパニ− | Purification of somatotropin from transformed microorganisms. |
| US4766224A (en) * | 1985-08-19 | 1988-08-23 | International Minerals & Chemical Corp. | Purification and activation of proteins from insoluble inclusion bodies |
| US4677196A (en) * | 1985-09-06 | 1987-06-30 | International Minerals & Chemical Corp. | Purification and activation of proteins from insoluble inclusion bodies |
| US4766205A (en) * | 1985-11-13 | 1988-08-23 | Beatrice Companies, Inc. | Method for isolation of recombinant polypeptides in biologically active forms |
| AU597924B2 (en) * | 1985-12-11 | 1990-06-14 | Natinco Nv | Solubilization of protein aggregates |
| US4888416A (en) * | 1987-03-30 | 1989-12-19 | International Minerals & Chemical Corp. | Method for stabilizing somatotropins |
| EP0295859B1 (en) * | 1987-06-15 | 1994-11-17 | Southern Cross Biotech Pty.Ltd. | Production of proteins in active forms |
| US4985544A (en) * | 1987-08-04 | 1991-01-15 | Kyowa Hakko Kogyo Co., Ltd. | Process for renaturing fish growth hormone |
| JPH01132598A (en) * | 1987-10-14 | 1989-05-25 | Pitman Moore Inc | Method for promoting production of intramolecular disulfide bond in recominant protein contained in modifier solution |
| US4975529A (en) * | 1989-08-18 | 1990-12-04 | Monsanto Company | Method of folding somatotropins |
| US5182369A (en) * | 1990-02-28 | 1993-01-26 | Monsanto Company | Method for purifying somatotropin monomers |
| US5109117A (en) * | 1990-06-26 | 1992-04-28 | Monsanto Company | Method of somatotropin naturation using urea and a soluble organic alcohol |
| US5023323A (en) * | 1990-09-12 | 1991-06-11 | Monsanto Company | Method of somatotropin naturation |
| US5240834A (en) * | 1991-01-22 | 1993-08-31 | Albert Einstein College Of Medicine Of Yeshiva University | Solubilization of protein after bacterial expression using sarkosyl |
| SE9201073D0 (en) * | 1992-04-03 | 1992-04-03 | Kabi Pharmacia Ab | PROTEIN FORMULATION |
| DE69426570T2 (en) * | 1993-11-03 | 2001-08-23 | Isomed Inc | MICELLOUS FINE-PARTIAL PHARMACEUTICAL COMPOSITIONS |
| DE69434626D1 (en) * | 1993-11-17 | 2006-04-20 | Athena Neurosciences Inc | TRANSPARENT LIQUID FOR THE ADMINISTRATION OF CAPTIVATED MEDICAMENTS |
| ZA9711733B (en) * | 1996-12-31 | 1998-07-01 | Monsanto Co | Method for solubilization and naturation of somatotropins |
-
1997
- 1997-12-30 ZA ZA9711733A patent/ZA9711733B/en unknown
- 1997-12-31 KR KR10-1999-7005951A patent/KR100487299B1/en not_active IP Right Cessation
- 1997-12-31 JP JP53035698A patent/JP2001509793A/en active Pending
- 1997-12-31 CA CA002276252A patent/CA2276252A1/en not_active Abandoned
- 1997-12-31 EP EP97955015A patent/EP0948540A2/en not_active Withdrawn
- 1997-12-31 WO PCT/US1997/024287 patent/WO1998029433A2/en active IP Right Grant
- 1997-12-31 AU AU69370/98A patent/AU6937098A/en not_active Abandoned
- 1997-12-31 US US09/002,565 patent/US6034224A/en not_active Expired - Lifetime
-
1999
- 1999-12-15 US US09/461,784 patent/US6410694B1/en not_active Expired - Lifetime
-
2001
- 2001-11-02 US US10/002,084 patent/US6562951B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| EP0948540A2 (en) | 1999-10-13 |
| WO1998029433A2 (en) | 1998-07-09 |
| US6562951B2 (en) | 2003-05-13 |
| KR20000069805A (en) | 2000-11-25 |
| US6034224A (en) | 2000-03-07 |
| AU6937098A (en) | 1998-07-31 |
| KR100487299B1 (en) | 2005-05-03 |
| US20020058792A1 (en) | 2002-05-16 |
| JP2001509793A (en) | 2001-07-24 |
| WO1998029433A3 (en) | 1998-10-15 |
| ZA9711733B (en) | 1998-07-01 |
| US6410694B1 (en) | 2002-06-25 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request | ||
| FZDE | Discontinued | ||
| FZDE | Discontinued |
Effective date: 20070102 |