MA40232A - Procédé de purification de la protéine de fusion tnfr:fc - Google Patents
Procédé de purification de la protéine de fusion tnfr:fcInfo
- Publication number
- MA40232A MA40232A MA040232A MA40232A MA40232A MA 40232 A MA40232 A MA 40232A MA 040232 A MA040232 A MA 040232A MA 40232 A MA40232 A MA 40232A MA 40232 A MA40232 A MA 40232A
- Authority
- MA
- Morocco
- Prior art keywords
- tnfr
- fusion protein
- purification
- present
- hcp
- Prior art date
Links
- 108091006020 Fc-tagged proteins Proteins 0.000 title abstract 4
- 238000000746 purification Methods 0.000 title abstract 3
- 238000000034 method Methods 0.000 title abstract 2
- 102000004190 Enzymes Human genes 0.000 abstract 1
- 108090000790 Enzymes Proteins 0.000 abstract 1
- 238000001042 affinity chromatography Methods 0.000 abstract 1
- 230000000593 degrading effect Effects 0.000 abstract 1
- 238000012434 mixed-mode chromatography Methods 0.000 abstract 1
- 108090000623 proteins and genes Proteins 0.000 abstract 1
- 102000004169 proteins and genes Human genes 0.000 abstract 1
Classifications
-
- 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
- C07K14/705—Receptors; Cell surface antigens; Cell surface determinants
- C07K14/715—Receptors; Cell surface antigens; Cell surface determinants for cytokines; for lymphokines; for interferons
- C07K14/7151—Receptors; Cell surface antigens; Cell surface determinants for cytokines; for lymphokines; for interferons for tumor necrosis factor [TNF], for lymphotoxin [LT]
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D15/00—Separating processes involving the treatment of liquids with solid sorbents; Apparatus therefor
- B01D15/08—Selective adsorption, e.g. chromatography
- B01D15/10—Selective adsorption, e.g. chromatography characterised by constructional or operational features
- B01D15/12—Selective adsorption, e.g. chromatography characterised by constructional or operational features relating to the preparation of the feed
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D15/00—Separating processes involving the treatment of liquids with solid sorbents; Apparatus therefor
- B01D15/08—Selective adsorption, e.g. chromatography
- B01D15/10—Selective adsorption, e.g. chromatography characterised by constructional or operational features
- B01D15/20—Selective adsorption, e.g. chromatography characterised by constructional or operational features relating to the conditioning of the sorbent material
- B01D15/203—Equilibration or regeneration
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D15/00—Separating processes involving the treatment of liquids with solid sorbents; Apparatus therefor
- B01D15/08—Selective adsorption, e.g. chromatography
- B01D15/26—Selective adsorption, e.g. chromatography characterised by the separation mechanism
- B01D15/30—Partition chromatography
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D15/00—Separating processes involving the treatment of liquids with solid sorbents; Apparatus therefor
- B01D15/08—Selective adsorption, e.g. chromatography
- B01D15/26—Selective adsorption, e.g. chromatography characterised by the separation mechanism
- B01D15/36—Selective adsorption, e.g. chromatography characterised by the separation mechanism involving ionic interaction, e.g. ion-exchange, ion-pair, ion-suppression or ion-exclusion
- B01D15/361—Ion-exchange
- B01D15/363—Anion-exchange
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D15/00—Separating processes involving the treatment of liquids with solid sorbents; Apparatus therefor
- B01D15/08—Selective adsorption, e.g. chromatography
- B01D15/26—Selective adsorption, e.g. chromatography characterised by the separation mechanism
- B01D15/38—Selective adsorption, e.g. chromatography characterised by the separation mechanism involving specific interaction not covered by one or more of groups B01D15/265 and B01D15/30 - B01D15/36, e.g. affinity, ligand exchange or chiral chromatography
- B01D15/3804—Affinity chromatography
- B01D15/3809—Affinity chromatography of the antigen-antibody type, e.g. protein A, G or L chromatography
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D15/00—Separating processes involving the treatment of liquids with solid sorbents; Apparatus therefor
- B01D15/08—Selective adsorption, e.g. chromatography
- B01D15/26—Selective adsorption, e.g. chromatography characterised by the separation mechanism
- B01D15/38—Selective adsorption, e.g. chromatography characterised by the separation mechanism involving specific interaction not covered by one or more of groups B01D15/265 and B01D15/30 - B01D15/36, e.g. affinity, ligand exchange or chiral chromatography
- B01D15/3847—Multimodal interactions
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D15/00—Separating processes involving the treatment of liquids with solid sorbents; Apparatus therefor
- B01D15/08—Selective adsorption, e.g. chromatography
- B01D15/42—Selective adsorption, e.g. chromatography characterised by the development mode, e.g. by displacement or by elution
- B01D15/424—Elution mode
-
- 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
- C07K14/705—Receptors; Cell surface antigens; Cell surface determinants
- C07K14/70578—NGF-receptor/TNF-receptor superfamily, e.g. CD27, CD30, CD40, CD95
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2319/00—Fusion polypeptide
- C07K2319/30—Non-immunoglobulin-derived peptide or protein having an immunoglobulin constant or Fc region, or a fragment thereof, attached thereto
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Analytical Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Molecular Biology (AREA)
- Immunology (AREA)
- Cell Biology (AREA)
- Gastroenterology & Hepatology (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Medicinal Chemistry (AREA)
- Zoology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Toxicology (AREA)
- Peptides Or Proteins (AREA)
- Enzymes And Modification Thereof (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Abstract
La présente invention concerne la purification de la protéine de fusion tnfr:fc. L'invention concerne, plus précisément, un procédé de purification de la protéine de fusion tnfr:fc, caractérisé par une réduction du niveau des protéines des cellules hôtes (hcp). La présente invention concerne l'utilisation de la chromatographie en mode mixte et/ou de la chromatographie d'affinité pour produire une protéine de fusion tnfr:fc sensiblement exempte d'au moins l'une des enzymes de dégradation des protéines présentes dans les hcp.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IN1919MU2014 | 2014-06-13 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA40232A true MA40232A (fr) | 2017-04-19 |
Family
ID=53524922
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA040232A MA40232A (fr) | 2014-06-13 | 2015-06-13 | Procédé de purification de la protéine de fusion tnfr:fc |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US10556942B2 (fr) |
| EP (1) | EP3155009A1 (fr) |
| JP (1) | JP6747985B2 (fr) |
| CN (1) | CN106536565A (fr) |
| AU (1) | AU2015273049B2 (fr) |
| BR (1) | BR112016029157A8 (fr) |
| CA (1) | CA2951766A1 (fr) |
| MA (1) | MA40232A (fr) |
| MX (1) | MX2016016318A (fr) |
| PH (1) | PH12016502482A1 (fr) |
| RU (1) | RU2698654C2 (fr) |
| WO (1) | WO2015189832A1 (fr) |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11566082B2 (en) | 2014-11-17 | 2023-01-31 | Cytiva Bioprocess R&D Ab | Mutated immunoglobulin-binding polypeptides |
| KR20170138426A (ko) * | 2015-03-13 | 2017-12-15 | 삼성바이오에피스 주식회사 | 항-tnf-알파 폴리펩티드 조성물 및 그 용도 |
| US10889615B2 (en) | 2016-05-11 | 2021-01-12 | Cytiva Bioprocess R&D Ab | Mutated immunoglobulin-binding polypeptides |
| CN109311948B (zh) | 2016-05-11 | 2022-09-16 | 思拓凡生物工艺研发有限公司 | 清洁和/或消毒分离基质的方法 |
| US10703774B2 (en) | 2016-09-30 | 2020-07-07 | Ge Healthcare Bioprocess R&D Ab | Separation method |
| JP7031934B2 (ja) | 2016-05-11 | 2022-03-08 | サイティバ・バイオプロセス・アールアンドディ・アクチボラグ | 分離マトリックス |
| US10654887B2 (en) | 2016-05-11 | 2020-05-19 | Ge Healthcare Bio-Process R&D Ab | Separation matrix |
| US10730908B2 (en) | 2016-05-11 | 2020-08-04 | Ge Healthcare Bioprocess R&D Ab | Separation method |
| EP3455243B1 (fr) | 2016-05-11 | 2021-03-24 | Cytiva BioProcess R&D AB | Matrice de séparation |
| EP3455240B1 (fr) | 2016-05-11 | 2025-01-01 | Cytiva BioProcess R&D AB | Procédé de conservation d'une matrice de séparation |
| US12448411B2 (en) | 2016-09-30 | 2025-10-21 | Cytiva Bioprocess R&D Ab | Separation method |
| MY199833A (en) * | 2017-08-17 | 2023-11-24 | Just Evotec Biologics Inc | Method of purifying glycosylated protein from host cell galectins and other contaminants |
| CA3072129A1 (fr) * | 2017-08-30 | 2019-03-07 | Ares Trading S.A. | Procede de purification de proteines |
| US11952399B2 (en) * | 2018-12-18 | 2024-04-09 | Amgen Inc. | Methods for purifying proteins |
| EP3917951A1 (fr) * | 2019-01-30 | 2021-12-08 | Amgen, Inc | Attributs de l'aflibercept et leurs procédés de caractérisation et de modification |
| KR102286892B1 (ko) * | 2019-07-08 | 2021-08-06 | 삼천당제약주식회사 | 안과용 단백질 제제의 정제방법 |
| CN112876567A (zh) * | 2019-11-29 | 2021-06-01 | 广东菲鹏制药股份有限公司 | Fc融合蛋白及其纯化方法 |
| US20230357315A1 (en) * | 2020-03-11 | 2023-11-09 | Dr. Reddy's Laboratories Limited | METHOD OF PURIFYING AN Fc-FUSION PROTEIN |
| CN113563469A (zh) * | 2020-04-28 | 2021-10-29 | 江苏中新医药有限公司 | 高回收率纯化阿达木单抗的方法 |
| WO2022234412A1 (fr) * | 2021-05-03 | 2022-11-10 | Lupin Limited | Procédé de purification de protéines de fusion fc |
| EP4408857A4 (fr) * | 2021-09-28 | 2025-11-05 | Kashiv Biosciences Llc | Procédé amélioré de purification de protéine de fusion |
| EP4408879A4 (fr) * | 2021-09-28 | 2025-08-27 | Kashiv Biosciences Llc | Procédé amélioré de purification de protéine de fusion |
| EP4408856A4 (fr) * | 2021-09-28 | 2025-11-12 | Kashiv Biosciences Llc | Procédé amélioré pour purification de protéine |
| CN118414350A (zh) * | 2021-10-19 | 2024-07-30 | 阿特根公司 | 纯化具有igg fc结构域的融合蛋白的方法 |
| US20250026784A1 (en) * | 2021-11-29 | 2025-01-23 | Tosoh Corporation | Separation method of antibody |
| CN119060168A (zh) * | 2024-09-26 | 2024-12-03 | 广东丸美生物技术股份有限公司 | 一种具有低电导率的重组胶原蛋白溶液及其制备方法和应用 |
Family Cites Families (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2021284C1 (ru) * | 1991-05-30 | 1994-10-15 | Всесоюзный научно-исследовательский институт технологии кровезаменителей и гормональных препаратов | Способ очистки клинических фракций декстрана |
| US7294481B1 (en) | 1999-01-05 | 2007-11-13 | Immunex Corporation | Method for producing recombinant proteins |
| EP1478394B1 (fr) | 2002-02-27 | 2008-07-30 | Immunex Corporation | Composition stabilisée comprenant TNFR-Fc et arginine |
| DK1601697T3 (da) | 2003-02-28 | 2007-10-01 | Lonza Biologics Plc | Oprensning af antistof ved protein A- og ionbytningskromatografi |
| WO2007109163A2 (fr) * | 2006-03-16 | 2007-09-27 | Amgen Inc | Tampon de lavage et procédé d'utilisation correspondant |
| JP2010501623A (ja) * | 2006-08-28 | 2010-01-21 | アレス トレーディング ソシエテ アノニム | Fc含有タンパク質の精製法 |
| JP2010501622A (ja) * | 2006-08-28 | 2010-01-21 | アレス トレーディング ソシエテ アノニム | Fc−融合タンパク質の精製法 |
| JP2011500757A (ja) * | 2007-10-22 | 2011-01-06 | メルク セローノ ソシエテ アノニム | Fc含有タンパク質の精製方法 |
| JP2011514895A (ja) * | 2008-02-29 | 2011-05-12 | バイオジェン・アイデック・エムエイ・インコーポレイテッド | 精製免疫グロブリン融合タンパク質およびその精製方法 |
| WO2010056550A1 (fr) | 2008-10-29 | 2010-05-20 | Wyeth Llc | Procédés de purification de molécules de liaison d’antigène monodomaines |
| CN102712673B (zh) * | 2010-01-22 | 2014-04-30 | 贝林格尔.英格海姆国际有限公司 | 用于纯化含fc的蛋白的色谱方法 |
| WO2012176158A1 (fr) | 2011-06-24 | 2012-12-27 | Dr. Reddy's Laboratories Limited | Purification de protéine chimérique |
| BR112014000352A2 (pt) * | 2011-07-08 | 2017-02-14 | Merck Sharp & Dohe Corp | método de purificar uma proteína de fusão-fc, proteínas de fusão contendo fc purificada, tnfr:fc purificada, e tnfr:fc elevadamente purificada |
| EP2753634B1 (fr) * | 2011-08-17 | 2017-11-01 | Ares Trading S.A. | Procédé de préparation d'une forme active de la protéine de fusion tnfr-fc |
| US9249182B2 (en) | 2012-05-24 | 2016-02-02 | Abbvie, Inc. | Purification of antibodies using hydrophobic interaction chromatography |
| PE20150996A1 (es) * | 2012-09-11 | 2015-08-01 | Coherus Biosciences Inc | Etanercept correctamente plegado de alta pureza y excelente rendimiento |
| CN102911250B (zh) * | 2012-09-29 | 2014-04-16 | 浙江海正药业股份有限公司 | 酸性重组蛋白药物的纯化方法 |
| US9649383B2 (en) * | 2012-11-19 | 2017-05-16 | Merck Sharp & Dohme Corp. | Liquid formulations for TNFR:Fc fusion proteins |
| LT2969099T (lt) * | 2013-03-14 | 2018-09-10 | Amgen Inc. | Pratekėjusio ligando pašalinimas afininiame gryninime |
| US8946395B1 (en) * | 2013-10-18 | 2015-02-03 | Abbvie Inc. | Purification of proteins using hydrophobic interaction chromatography |
-
2015
- 2015-06-13 CN CN201580038801.XA patent/CN106536565A/zh active Pending
- 2015-06-13 MA MA040232A patent/MA40232A/fr unknown
- 2015-06-13 EP EP15734731.1A patent/EP3155009A1/fr not_active Withdrawn
- 2015-06-13 US US15/318,489 patent/US10556942B2/en active Active
- 2015-06-13 CA CA2951766A patent/CA2951766A1/fr not_active Abandoned
- 2015-06-13 BR BR112016029157A patent/BR112016029157A8/pt not_active Application Discontinuation
- 2015-06-13 JP JP2016572703A patent/JP6747985B2/ja not_active Expired - Fee Related
- 2015-06-13 MX MX2016016318A patent/MX2016016318A/es unknown
- 2015-06-13 RU RU2017100005A patent/RU2698654C2/ru active
- 2015-06-13 AU AU2015273049A patent/AU2015273049B2/en not_active Ceased
- 2015-06-13 WO PCT/IB2015/054494 patent/WO2015189832A1/fr not_active Ceased
-
2016
- 2016-12-13 PH PH12016502482A patent/PH12016502482A1/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CN106536565A (zh) | 2017-03-22 |
| RU2698654C2 (ru) | 2019-08-28 |
| EP3155009A1 (fr) | 2017-04-19 |
| US20170152298A1 (en) | 2017-06-01 |
| AU2015273049B2 (en) | 2019-11-14 |
| BR112016029157A2 (pt) | 2017-08-22 |
| RU2017100005A (ru) | 2018-07-13 |
| JP6747985B2 (ja) | 2020-08-26 |
| MX2016016318A (es) | 2017-06-12 |
| CA2951766A1 (fr) | 2015-12-17 |
| US10556942B2 (en) | 2020-02-11 |
| JP2017521389A (ja) | 2017-08-03 |
| AU2015273049A1 (en) | 2017-01-12 |
| PH12016502482A1 (en) | 2017-04-10 |
| BR112016029157A8 (pt) | 2021-07-06 |
| WO2015189832A1 (fr) | 2015-12-17 |
| RU2017100005A3 (fr) | 2019-02-28 |
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