ZA200300642B - Process for folding chemically synthesized polypeptides. - Google Patents
Process for folding chemically synthesized polypeptides. Download PDFInfo
- Publication number
- ZA200300642B ZA200300642B ZA200300642A ZA200300642A ZA200300642B ZA 200300642 B ZA200300642 B ZA 200300642B ZA 200300642 A ZA200300642 A ZA 200300642A ZA 200300642 A ZA200300642 A ZA 200300642A ZA 200300642 B ZA200300642 B ZA 200300642B
- Authority
- ZA
- South Africa
- Prior art keywords
- cysteine
- folding
- polypeptide
- temperature
- folding buffer
- Prior art date
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- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 230000006334 disulfide bridging Effects 0.000 description 1
- 150000002019 disulfides Chemical class 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 239000002532 enzyme inhibitor Substances 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 1
- 238000002523 gelfiltration Methods 0.000 description 1
- 239000005556 hormone Substances 0.000 description 1
- 229940088597 hormone Drugs 0.000 description 1
- 238000002013 hydrophilic interaction chromatography Methods 0.000 description 1
- 238000004191 hydrophobic interaction chromatography Methods 0.000 description 1
- NPZTUJOABDZTLV-UHFFFAOYSA-N hydroxybenzotriazole Substances O=C1C=CC=C2NNN=C12 NPZTUJOABDZTLV-UHFFFAOYSA-N 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 238000004949 mass spectrometry Methods 0.000 description 1
- 230000001404 mediated effect Effects 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- 210000000440 neutrophil Anatomy 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 238000006384 oligomerization reaction Methods 0.000 description 1
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 1
- YPZRWBKMTBYPTK-UHFFFAOYSA-N oxidized gamma-L-glutamyl-L-cysteinylglycine Natural products OC(=O)C(N)CCC(=O)NC(C(=O)NCC(O)=O)CSSCC(C(=O)NCC(O)=O)NC(=O)CCC(N)C(O)=O YPZRWBKMTBYPTK-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 238000010647 peptide synthesis reaction Methods 0.000 description 1
- 125000001151 peptidyl group Chemical group 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 108010026466 polyproline Proteins 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000002953 preparative HPLC Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 108020003519 protein disulfide isomerase Proteins 0.000 description 1
- 230000012846 protein folding Effects 0.000 description 1
- 239000013014 purified material Substances 0.000 description 1
- 239000012264 purified product Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 238000004366 reverse phase liquid chromatography Methods 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- PCMORTLOPMLEFB-ONEGZZNKSA-N sinapic acid Chemical compound COC1=CC(\C=C\C(O)=O)=CC(OC)=C1O PCMORTLOPMLEFB-ONEGZZNKSA-N 0.000 description 1
- PCMORTLOPMLEFB-UHFFFAOYSA-N sinapinic acid Natural products COC1=CC(C=CC(O)=O)=CC(OC)=C1O PCMORTLOPMLEFB-UHFFFAOYSA-N 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000003774 sulfhydryl reagent Substances 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 229910052716 thallium Inorganic materials 0.000 description 1
- BKVIYDNLLOSFOA-UHFFFAOYSA-N thallium Chemical compound [Tl] BKVIYDNLLOSFOA-UHFFFAOYSA-N 0.000 description 1
- 230000034005 thiol-disulfide exchange Effects 0.000 description 1
- 150000007944 thiolates Chemical class 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 239000003053 toxin Substances 0.000 description 1
- 231100000765 toxin Toxicity 0.000 description 1
- 108700012359 toxins Proteins 0.000 description 1
- 125000000430 tryptophan group Chemical group [H]N([H])C(C(=O)O*)C([H])([H])C1=C([H])N([H])C2=C([H])C([H])=C([H])C([H])=C12 0.000 description 1
Classifications
-
- 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
- C07K1/107—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length by chemical modification of precursor peptides
- C07K1/113—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length by chemical modification of precursor peptides without change of the primary structure
-
- 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
- C07K1/107—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length by chemical modification of precursor peptides
- C07K1/113—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length by chemical modification of precursor peptides without change of the primary structure
- C07K1/1133—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length by chemical modification of precursor peptides without change of the primary structure by redox-reactions involving cystein/cystin side chains
-
- 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
- C07K1/04—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length on carriers
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Analytical Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Peptides Or Proteins (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP00204207 | 2000-11-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200300642B true ZA200300642B (en) | 2004-07-16 |
Family
ID=8172340
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200300642A ZA200300642B (en) | 2000-11-27 | 2003-01-23 | Process for folding chemically synthesized polypeptides. |
Country Status (22)
| Country | Link |
|---|---|
| US (2) | US20020082384A1 (zh) |
| EP (2) | EP1679318A1 (zh) |
| JP (1) | JP2004516300A (zh) |
| KR (1) | KR20030081315A (zh) |
| CN (2) | CN1249078C (zh) |
| AT (1) | ATE322501T1 (zh) |
| AU (2) | AU2002229603B2 (zh) |
| BR (1) | BR0113091A (zh) |
| CA (1) | CA2416054A1 (zh) |
| CU (1) | CU23034A3 (zh) |
| DE (1) | DE60118598T2 (zh) |
| DK (1) | DK1337549T3 (zh) |
| ES (1) | ES2261509T4 (zh) |
| HU (1) | HUP0302395A3 (zh) |
| IL (1) | IL155506A0 (zh) |
| MX (1) | MXPA03003576A (zh) |
| NO (1) | NO20032356D0 (zh) |
| NZ (1) | NZ523679A (zh) |
| PL (1) | PL364932A1 (zh) |
| RU (1) | RU2275377C2 (zh) |
| WO (1) | WO2002050099A2 (zh) |
| ZA (1) | ZA200300642B (zh) |
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7091310B2 (en) * | 2002-09-13 | 2006-08-15 | Chemokine Therapeutics Corporation | Chemokine analogs for the treatment of human disease |
| US7214660B2 (en) | 2001-10-10 | 2007-05-08 | Neose Technologies, Inc. | Erythropoietin: remodeling and glycoconjugation of erythropoietin |
| US7173003B2 (en) | 2001-10-10 | 2007-02-06 | Neose Technologies, Inc. | Granulocyte colony stimulating factor: remodeling and glycoconjugation of G-CSF |
| EP1615945B1 (en) | 2003-04-09 | 2011-09-28 | BioGeneriX AG | Glycopegylation methods and proteins/peptides produced by the methods |
| US9005625B2 (en) | 2003-07-25 | 2015-04-14 | Novo Nordisk A/S | Antibody toxin conjugates |
| US20080305992A1 (en) | 2003-11-24 | 2008-12-11 | Neose Technologies, Inc. | Glycopegylated erythropoietin |
| EP1807442A1 (en) * | 2004-10-26 | 2007-07-18 | Lonza Ag | S-alkyl-sulphenyl protection groups in solid-phase synthesis |
| US20080176790A1 (en) | 2004-10-29 | 2008-07-24 | Defrees Shawn | Remodeling and Glycopegylation of Fibroblast Growth Factor (Fgf) |
| US9029331B2 (en) | 2005-01-10 | 2015-05-12 | Novo Nordisk A/S | Glycopegylated granulocyte colony stimulating factor |
| US20070154992A1 (en) | 2005-04-08 | 2007-07-05 | Neose Technologies, Inc. | Compositions and methods for the preparation of protease resistant human growth hormone glycosylation mutants |
| EP1893632B1 (en) * | 2005-06-17 | 2015-08-12 | Novo Nordisk Health Care AG | Selective reduction and derivatization of engineered factor vii proteins comprising at least one non-native cysteine |
| US20070105755A1 (en) | 2005-10-26 | 2007-05-10 | Neose Technologies, Inc. | One pot desialylation and glycopegylation of therapeutic peptides |
| US20090048440A1 (en) | 2005-11-03 | 2009-02-19 | Neose Technologies, Inc. | Nucleotide Sugar Purification Using Membranes |
| US20090081145A1 (en) * | 2005-12-23 | 2009-03-26 | Aplagen Gmbh | Process for forming disulphide bridges |
| AU2007248855A1 (en) * | 2006-05-03 | 2007-11-15 | Mallinckrodt Inc. | Composition and method for the release of protected peptides from a resin |
| US20080242607A1 (en) | 2006-07-21 | 2008-10-02 | Neose Technologies, Inc. | Glycosylation of peptides via o-linked glycosylation sequences |
| US20100075375A1 (en) | 2006-10-03 | 2010-03-25 | Novo Nordisk A/S | Methods for the purification of polypeptide conjugates |
| WO2008077621A1 (de) * | 2006-12-23 | 2008-07-03 | Aplagen Gmbh | Verfahren zur ausbildung von disulfidbrücken |
| KR20100016160A (ko) | 2007-04-03 | 2010-02-12 | 바이오제너릭스 에이지 | 글리코페길화 ｇ―ｃｓｆ를 이용하는 치료 방법 |
| MX2009013259A (es) | 2007-06-12 | 2010-01-25 | Novo Nordisk As | Proceso mejorado para la produccion de azucares de nucleotidos. |
| US20130189239A1 (en) | 2008-02-27 | 2013-07-25 | Novo Nordisk A/S | Conjugated Factor VIII Molecules |
| CN104844693B (zh) * | 2015-06-10 | 2018-08-03 | 成都圣诺生物科技股份有限公司 | 一种合成利那洛肽的方法 |
| CN111655314B (zh) | 2018-02-02 | 2022-11-18 | 诺和诺德股份有限公司 | 具有可偏转换能器的药物注射装置 |
| CN111100188A (zh) * | 2018-10-25 | 2020-05-05 | 成都医学院 | 一种制备蜘蛛抗菌肽的方法 |
| CN109593119A (zh) * | 2019-01-27 | 2019-04-09 | 上海丽珠制药有限公司 | 一种[2-d-组氨酸]-醋酸亮丙瑞林的制备方法 |
| JP7453745B2 (ja) * | 2019-03-28 | 2024-03-21 | 株式会社ヤクルト本社 | 毒性タンパク質の活性を阻害するペプチドのスクリーニング方法及び毒性タンパク質の製造方法 |
| CN110845595A (zh) * | 2019-11-14 | 2020-02-28 | 连云港职业技术学院 | 一种固相合成5-tmara标记的铁调素-25的方法 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2923787A1 (de) * | 1979-06-12 | 1980-12-18 | Max Planck Gesellschaft | Verfahren zur selektiven bildung von disulfidbruecken in polypeptiden und die dabei erhaltenen produkte als wirkstoffe enthaltende arzneimittel |
| DE3236849A1 (de) * | 1982-10-05 | 1984-04-05 | Max Planck Gesellschaft zur Förderung der Wissenschaften e.V., 3400 Göttingen | Neue thiohydrazin-1,2-dicarbonsaeure-derivate, verfahren zu ihrer herstellung und ihre verwendung |
| IL96682A0 (en) * | 1989-12-15 | 1991-09-16 | Amgen Inc | Production of biologically active platelet-derived growth factor from high expression host cell systems |
| CA2072249C (en) * | 1991-06-28 | 2003-06-17 | Saiko Hosokawa | Human monoclonal antibody specifically binding to surface antigen of cancer cell membrane |
| CN1105029A (zh) * | 1993-05-24 | 1995-07-12 | 花王株式会社 | 制备溶解蛋白质的方法 |
| US5663304A (en) * | 1993-08-20 | 1997-09-02 | Genentech, Inc. | Refolding of misfolded insulin-like growth factor-I |
| DE4431317A1 (de) * | 1994-09-02 | 1996-03-07 | Biotechnolog Forschung Gmbh | Schutz- bzw. Ankergruppen und deren Verwendung |
-
2001
- 2001-11-27 DK DK01990489T patent/DK1337549T3/da active
- 2001-11-27 KR KR10-2003-7004957A patent/KR20030081315A/ko not_active Application Discontinuation
- 2001-11-27 AU AU2002229603A patent/AU2002229603B2/en not_active Expired - Fee Related
- 2001-11-27 BR BR0113091-9A patent/BR0113091A/pt not_active IP Right Cessation
- 2001-11-27 WO PCT/EP2001/014163 patent/WO2002050099A2/en active IP Right Grant
- 2001-11-27 PL PL01364932A patent/PL364932A1/xx not_active Application Discontinuation
- 2001-11-27 HU HU0302395A patent/HUP0302395A3/hu unknown
- 2001-11-27 DE DE60118598T patent/DE60118598T2/de not_active Expired - Fee Related
- 2001-11-27 JP JP2002551992A patent/JP2004516300A/ja active Pending
- 2001-11-27 NZ NZ523679A patent/NZ523679A/en unknown
- 2001-11-27 CN CNB018147968A patent/CN1249078C/zh not_active Expired - Fee Related
- 2001-11-27 RU RU2003119075/04A patent/RU2275377C2/ru not_active IP Right Cessation
- 2001-11-27 EP EP06075237A patent/EP1679318A1/en not_active Withdrawn
- 2001-11-27 EP EP01990489A patent/EP1337549B1/en not_active Expired - Lifetime
- 2001-11-27 US US09/995,335 patent/US20020082384A1/en not_active Abandoned
- 2001-11-27 AU AU2960302A patent/AU2960302A/xx active Pending
- 2001-11-27 AT AT01990489T patent/ATE322501T1/de not_active IP Right Cessation
- 2001-11-27 CU CU20030094A patent/CU23034A3/es unknown
- 2001-11-27 CA CA002416054A patent/CA2416054A1/en not_active Abandoned
- 2001-11-27 CN CNA2006100047520A patent/CN1830999A/zh active Pending
- 2001-11-27 MX MXPA03003576A patent/MXPA03003576A/es active IP Right Grant
- 2001-11-27 ES ES01990489T patent/ES2261509T4/es not_active Expired - Lifetime
- 2001-11-27 IL IL15550601A patent/IL155506A0/xx unknown
-
2003
- 2003-01-23 ZA ZA200300642A patent/ZA200300642B/en unknown
- 2003-05-26 NO NO20032356A patent/NO20032356D0/no unknown
-
2005
- 2005-05-19 US US11/132,987 patent/US20050239162A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| US20050239162A1 (en) | 2005-10-27 |
| ES2261509T4 (es) | 2008-02-16 |
| RU2275377C2 (ru) | 2006-04-27 |
| CN1249078C (zh) | 2006-04-05 |
| ATE322501T1 (de) | 2006-04-15 |
| DK1337549T3 (da) | 2006-07-31 |
| NO20032356L (no) | 2003-05-26 |
| HUP0302395A2 (hu) | 2003-10-28 |
| CA2416054A1 (en) | 2002-06-27 |
| DE60118598D1 (de) | 2006-05-18 |
| WO2002050099A2 (en) | 2002-06-27 |
| US20020082384A1 (en) | 2002-06-27 |
| JP2004516300A (ja) | 2004-06-03 |
| DE60118598T2 (de) | 2007-02-15 |
| ES2261509T3 (es) | 2006-11-16 |
| EP1337549B1 (en) | 2006-04-05 |
| NZ523679A (en) | 2005-10-28 |
| KR20030081315A (ko) | 2003-10-17 |
| BR0113091A (pt) | 2003-07-08 |
| CN1449406A (zh) | 2003-10-15 |
| MXPA03003576A (es) | 2003-10-14 |
| HUP0302395A3 (en) | 2007-05-02 |
| AU2002229603B2 (en) | 2007-11-08 |
| EP1337549A2 (en) | 2003-08-27 |
| AU2960302A (en) | 2002-07-01 |
| NO20032356D0 (no) | 2003-05-26 |
| CN1830999A (zh) | 2006-09-13 |
| PL364932A1 (en) | 2004-12-27 |
| EP1679318A1 (en) | 2006-07-12 |
| IL155506A0 (en) | 2003-11-23 |
| WO2002050099A3 (en) | 2002-09-19 |
| CU23034A3 (es) | 2005-03-22 |
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