KR900701823A - 혈장단백질의 크로마토그래피 분리법 - Google Patents
혈장단백질의 크로마토그래피 분리법Info
- Publication number
- KR900701823A KR900701823A KR1019900700239A KR900700239A KR900701823A KR 900701823 A KR900701823 A KR 900701823A KR 1019900700239 A KR1019900700239 A KR 1019900700239A KR 900700239 A KR900700239 A KR 900700239A KR 900701823 A KR900701823 A KR 900701823A
- Authority
- KR
- South Korea
- Prior art keywords
- factor
- buffer
- concentrate
- plasma
- fibronectin
- Prior art date
Links
- 108010017384 Blood Proteins Proteins 0.000 title claims 2
- 102000004506 Blood Proteins Human genes 0.000 title claims 2
- 238000013375 chromatographic separation Methods 0.000 title 1
- 238000000034 method Methods 0.000 claims 13
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims 6
- 239000000872 buffer Substances 0.000 claims 6
- 102000016359 Fibronectins Human genes 0.000 claims 4
- 108010067306 Fibronectins Proteins 0.000 claims 4
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 claims 4
- 239000012141 concentrate Substances 0.000 claims 4
- 238000004587 chromatography analysis Methods 0.000 claims 3
- 239000003480 eluent Substances 0.000 claims 3
- 230000002779 inactivation Effects 0.000 claims 3
- 239000011347 resin Substances 0.000 claims 3
- 229920005989 resin Polymers 0.000 claims 3
- 239000011780 sodium chloride Substances 0.000 claims 3
- 239000004471 Glycine Substances 0.000 claims 2
- 239000004472 Lysine Substances 0.000 claims 2
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 claims 2
- 238000011210 chromatographic step Methods 0.000 claims 2
- 239000002244 precipitate Substances 0.000 claims 2
- 238000000926 separation method Methods 0.000 claims 2
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical group CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 claims 1
- 102100023804 Coagulation factor VII Human genes 0.000 claims 1
- 108010023321 Factor VII Proteins 0.000 claims 1
- 108010049003 Fibrinogen Proteins 0.000 claims 1
- 102000008946 Fibrinogen Human genes 0.000 claims 1
- 229920002684 Sepharose Polymers 0.000 claims 1
- 241000700605 Viruses Species 0.000 claims 1
- 239000003957 anion exchange resin Substances 0.000 claims 1
- 238000005119 centrifugation Methods 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 238000001816 cooling Methods 0.000 claims 1
- 239000012149 elution buffer Substances 0.000 claims 1
- 229940012413 factor vii Drugs 0.000 claims 1
- 229940012952 fibrinogen Drugs 0.000 claims 1
- 239000000535 fibrinogen concentrate Substances 0.000 claims 1
- 238000002523 gelfiltration Methods 0.000 claims 1
- 230000002209 hydrophobic effect Effects 0.000 claims 1
- 230000003993 interaction Effects 0.000 claims 1
- 102000004169 proteins and genes Human genes 0.000 claims 1
- 108090000623 proteins and genes Proteins 0.000 claims 1
- 238000011403 purification operation Methods 0.000 claims 1
- 239000006228 supernatant Substances 0.000 claims 1
- 229920002554 vinyl polymer Polymers 0.000 claims 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
- C07K14/745—Blood coagulation or fibrinolysis factors
- C07K14/755—Factors VIII, e.g. factor VIII C (AHF), factor VIII Ag (VWF)
-
- 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
- C07K1/14—Extraction; Separation; Purification
- C07K1/16—Extraction; Separation; Purification by chromatography
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Biophysics (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Zoology (AREA)
- Hematology (AREA)
- Toxicology (AREA)
- Gastroenterology & Hepatology (AREA)
- Analytical Chemistry (AREA)
- Peptides Or Proteins (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (14)
- 혈장 저온침전물의 용해성분을 적절한 이온성 음이온 교환수지의 크로마토그래피 단계로 보내어 대형크기의 분자를 유지하고 소수성 상호작용을 일으키며 또한 용리완충액의 이온강도 증가에 따라 각각의 단백질을 선택적으로 회수하는 것을 특징으로 하는 인체 혹은 동물혈장 단백질 분리방법.
- 제1항에 있어서, 제 Ⅷ인자, 반 빌레브란드 인자, 피브로겐 및 피브로넥틴을 한유하는 혈장 저온침전물이 초기성분인 것을 특징으로 하는 분리방법.
- 제2항에 있어서, 초기성분에 들어있는 제 Ⅷ:C인자의 비활성이 0.1IU/㎎ 이상인 것을 특징으로 하는 방법.
- 제1항 내지 3항중 어느항에 있어서, 초기성분에 대하여 : -수산화 알루미늄으로 처리하고,-14-16℃로 냉각하며 또한,-원심분리하여 나온상청액을 수득하는 것으로된 사전-정제처리 작업을 실행하는 것을 특징으로 하는 방법.
- 제1항 내지 4항중 어느 항에 있어서, a) 저온 침전물의 용해성분을 제 Ⅷ인자, 다량의 반 빌레브란드 인자 및 피브로넥틴을 흡수하는 비닐고분자형 겔에 정착된 DEAE 그룹의 수지에 통과시키고 또한 피브리노겐을 용리액속으로 전달하며, b) 완충액의 이온강도를 1차 증가시켜 피브로넥틴 및 다량의 반빌레브란드 인자가 용리되도록 하고 또한, C) 완충액의 이온강도를 또다시 증가시켜 제 Ⅷ인자가 용리되도록 하는 단계를 특징으로 하는 방법.
- 제5항에 있어서, 완충액에 리신과 글리신이 들어었는 것을 특징으로 하는 방법.
- 제6항에 있어서, 완충액에 2 내지 4g/1의 리신과 8 내지 11g/1의 글리신이 들어있는 것을 특징으로 하는 방법.
- 제5항 내지 7항중 어느항에 있어서, 염화나트륨을 이용하여 완충액의 이온강도를 증가시키는 것을 특징으로 하는 방법.
- 제8항에 있어서 염화나트륨의 농도가 a) 단계의 경우는 0.11M이고 b) 단계에서는 0.15M이며 또한 C)단계의 경우는 O.25M인 것을 특징으로 하는 방법.
- 제1항 내지 9항중 어느항에 있어서, 화학적 비활성 작용제의 존재하의 혈장성분을 크로마토그래피 존재하의 혈장성분을 크로마토그래피 분리단계로 보내지 직전에 바이러스 비활성 처리하는 갓을 특징으로 하는 방법.
- 100 IU/㎎ 이상의 비활성으로 되며, 제2항 내지 1O항중 어느항에 따른 방법으로 형성한 것을 특징으로 하는 단일-그룹 농축물의 특성과 유사한 특성의 제 Ⅷ인자 농축물.
- 헤파린-세파로오스 수지에서의 부가적인 크로마토그래피 단계를 거쳐 정제되고 또한 제5항의 방법중 a) 단계의 용리액으로 된 것을 특징으로 하는 피브리노겐 농축물.
- a) 단계와 동일한 수지에서의 부가적인 크로마토그래피 단계를 거쳐 정제되고 0.15M의 NaCl로 조절된 완충액으로 용리하며, 또한 제5항의 방법중 b) 단계의 용리액으로 된 것을 특징으로 하는 반빌레브란드 인자 농축물.
- 부가적인 겔 여과단계를 거쳐 정제되며 또한 제5항의 방법중 b) 단계의 올리액으로된 것을 특징으로 하는 피브로넥틴 농축물.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR88.07503 | 1988-06-07 | ||
FR88.07530 | 1988-06-07 | ||
FR8807530A FR2632309B1 (fr) | 1988-06-07 | 1988-06-07 | Procede de purification par voie chromatographique de proteines, notamment de facteur viii, et les produits obtenus |
PCT/FR1989/000050 WO1989012065A1 (fr) | 1988-06-07 | 1989-02-08 | Separation chromatographique des proteines du plasma |
Publications (2)
Publication Number | Publication Date |
---|---|
KR900701823A true KR900701823A (ko) | 1990-12-04 |
KR970010923B1 KR970010923B1 (ko) | 1997-07-02 |
Family
ID=9367001
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019900700239A KR970010923B1 (ko) | 1988-06-07 | 1989-02-08 | 혈장단백질의 크로마토그래피 분리법 |
Country Status (17)
Country | Link |
---|---|
US (1) | US5252709A (ko) |
EP (1) | EP0359593B2 (ko) |
JP (1) | JP2805364B2 (ko) |
KR (1) | KR970010923B1 (ko) |
AT (1) | ATE121750T1 (ko) |
AU (2) | AU622436B2 (ko) |
CA (1) | CA1340742C (ko) |
DE (2) | DE68922358T3 (ko) |
DK (1) | DK175322B1 (ko) |
ES (1) | ES2070919T5 (ko) |
FI (1) | FI96210C (ko) |
FR (1) | FR2632309B1 (ko) |
LT (1) | LT3333B (ko) |
NO (1) | NO177188C (ko) |
RU (1) | RU1837880C (ko) |
UA (1) | UA11061A (ko) |
WO (1) | WO1989012065A1 (ko) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20150090252A (ko) * | 2012-12-05 | 2015-08-05 | 체에스엘 베링 게엠베하 | 치료학적 단백질의 정제 방법 |
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GB8729822D0 (en) * | 1987-12-22 | 1988-02-03 | Central Blood Lab Authority | Chemical process |
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FR2665449B1 (fr) * | 1990-08-02 | 1995-04-14 | Aquitaine Developp Transf Sang | Procede de fabrication de facteur von willebrand ayant une tres haute purete, depourvu en majeure partie de facteur antihemophilique (fviiic), et facteur von willebrand ainsi obtenu, ainsi qu'une composition pharmaceutique le contenant. |
DE3926034C3 (de) * | 1989-08-07 | 1996-11-21 | Behringwerke Ag | Verfahren zur Herstellung eines stabilen Faktors VIII |
FR2651437A1 (fr) * | 1989-09-05 | 1991-03-08 | Lille Transfusion Sanguine | Procede de preparation de concentre du complexe facteur viii-facteur von willebrand de la coagulation sanguine a partir de plasma total. |
NL9000090A (nl) * | 1990-01-15 | 1991-08-01 | Harimex Ligos Bv | Werkwijze voor het bereiden van een fibrinogeenconcentraat uit bloedplasma, inrichting voor het uitvoeren van deze werkwijze en werkwijze voor het bereiden van fibrinogeen uit het concentraat. |
FR2673632A1 (fr) * | 1991-03-08 | 1992-09-11 | Lille Transfusion Sanguine | Procede de preparation de concentre de facteur von willebrand humain de tres haute purete, approprie a un usage therapeutique. |
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DE4435485C1 (de) * | 1994-10-04 | 1996-03-21 | Immuno Ag | Verfahren zur Gewinnung von hochreinem von Willebrand-Faktor |
US5659017A (en) * | 1995-11-07 | 1997-08-19 | Alpha Therapeutic Corporation | Anion exchange process for the purification of Factor VIII |
AT403764B (de) | 1996-03-15 | 1998-05-25 | Immuno Ag | Stabiler faktor viii/vwf-komplex |
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US6037457A (en) * | 1997-01-31 | 2000-03-14 | The University Of North Carolina At Chapel Hill | Method for recombinant fibrinogen production |
AT405403B (de) | 1997-02-27 | 1999-08-25 | Immuno Ag | Reinigung von von willebrand-faktor durch kationenaustauscherchromatographie |
DE60035260T2 (de) | 1999-02-22 | 2007-10-18 | The University Of Connecticut, Farmington | Neue albuminfreie faktor viii formulierungen |
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FR2857267B1 (fr) | 2003-07-09 | 2006-03-10 | Lab Francais Du Fractionnement | Formulation stabilisante et solubilisante pour les proteines cryoprecipitables. |
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DE3609431A1 (de) * | 1986-03-20 | 1987-09-24 | Biotest Pharma Gmbh | Verfahren zur herstellung eines den blutgerinnungsfaktor viii enthaltenden, sterilen praeparates |
DE3707213A1 (de) * | 1987-03-06 | 1988-09-15 | Behringwerke Ag | Verfahren zur herstellung von faktor viii:c-mangelplasma und ein so erhaltenes mangelplasma |
US5043429B1 (en) * | 1987-05-01 | 1997-10-14 | Scripps Research Inst | Protein fragments containing factor VIII binding domain of von willebrand factor |
US5097018A (en) * | 1988-05-12 | 1992-03-17 | University Of Southern California | Sequential heat treatment of blood-clotting factor products |
NL8701915A (nl) * | 1987-08-14 | 1989-03-01 | Waander Riethorst | Adsorbensmateriaal en toepassing daarvan voor het isoleren van stollingsfaktoren. |
DE3904354A1 (de) * | 1989-02-14 | 1990-08-16 | Behringwerke Ag | Pasteurisiertes, gereinigtes von willebrand-faktor-konzentrat und verfahren zu seiner herstellung |
US5110907A (en) * | 1989-08-01 | 1992-05-05 | Alpha Therapeutic Corporation | Factor viii complex purification using heparin affinity chromatography |
IT1306645B1 (it) | 1999-04-08 | 2001-10-02 | Challenger Gestao E Consultado | Struttura di sedia, poltroncina o simile ad assemblaggio facilitato. |
-
1988
- 1988-06-07 FR FR8807530A patent/FR2632309B1/fr not_active Expired - Lifetime
-
1989
- 1989-02-08 US US07/460,972 patent/US5252709A/en not_active Expired - Lifetime
- 1989-02-08 WO PCT/FR1989/000050 patent/WO1989012065A1/fr active IP Right Grant
- 1989-02-08 AT AT89400348T patent/ATE121750T1/de not_active IP Right Cessation
- 1989-02-08 DE DE68922358T patent/DE68922358T3/de not_active Expired - Lifetime
- 1989-02-08 AU AU30682/89A patent/AU622436B2/en not_active Expired
- 1989-02-08 KR KR1019900700239A patent/KR970010923B1/ko not_active IP Right Cessation
- 1989-02-08 JP JP1502342A patent/JP2805364B2/ja not_active Expired - Lifetime
- 1989-02-08 EP EP89400348A patent/EP0359593B2/fr not_active Expired - Lifetime
- 1989-02-08 ES ES89400348T patent/ES2070919T5/es not_active Expired - Lifetime
- 1989-02-08 DE DE198989400348T patent/DE359593T1/de active Pending
- 1989-02-14 CA CA000590961A patent/CA1340742C/fr not_active Expired - Lifetime
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1990
- 1990-01-25 FI FI900397A patent/FI96210C/fi not_active IP Right Cessation
- 1990-02-05 NO NO900529A patent/NO177188C/no not_active IP Right Cessation
- 1990-02-06 UA UA4743107A patent/UA11061A/uk unknown
- 1990-02-06 DK DK199000299A patent/DK175322B1/da not_active IP Right Cessation
- 1990-02-06 RU SU904743107A patent/RU1837880C/ru active
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1992
- 1992-03-03 AU AU1138392A patent/AU1138392A/en active Pending
- 1992-12-29 LT LTIP262A patent/LT3333B/lt not_active IP Right Cessation
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20150090252A (ko) * | 2012-12-05 | 2015-08-05 | 체에스엘 베링 게엠베하 | 치료학적 단백질의 정제 방법 |
KR20210042422A (ko) * | 2012-12-05 | 2021-04-19 | 체에스엘 베링 게엠베하 | 치료학적 단백질의 정제 방법 |
Also Published As
Publication number | Publication date |
---|---|
WO1989012065A1 (fr) | 1989-12-14 |
DE68922358T3 (de) | 2004-08-19 |
FI96210B (fi) | 1996-02-15 |
FI900397A0 (fi) | 1990-01-25 |
AU3068289A (en) | 1990-01-05 |
DE359593T1 (de) | 1990-09-27 |
CA1340742C (fr) | 1999-09-14 |
DE68922358D1 (de) | 1995-06-01 |
NO900529L (no) | 1990-04-06 |
AU622436B2 (en) | 1992-04-09 |
EP0359593A1 (fr) | 1990-03-21 |
NO900529D0 (no) | 1990-02-05 |
RU1837880C (ru) | 1993-08-30 |
NO177188C (no) | 1995-08-02 |
ES2070919T5 (es) | 2004-07-16 |
EP0359593B1 (fr) | 1995-04-26 |
JPH03501974A (ja) | 1991-05-09 |
DK29990A (da) | 1990-03-28 |
JP2805364B2 (ja) | 1998-09-30 |
AU1138392A (en) | 1992-05-14 |
DK175322B1 (da) | 2004-08-23 |
ATE121750T1 (de) | 1995-05-15 |
NO177188B (no) | 1995-04-24 |
KR970010923B1 (ko) | 1997-07-02 |
DE68922358T2 (de) | 1995-10-12 |
DK29990D0 (da) | 1990-02-06 |
FI96210C (fi) | 1996-05-27 |
FR2632309B1 (fr) | 1990-08-24 |
US5252709A (en) | 1993-10-12 |
UA11061A (uk) | 1996-12-25 |
FR2632309A1 (fr) | 1989-12-08 |
LT3333B (en) | 1995-07-25 |
LTIP262A (en) | 1994-10-25 |
ES2070919T3 (es) | 1995-06-16 |
EP0359593B2 (fr) | 2004-01-07 |
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