DK1786273T3 - Sekventielle proteinisolerings- og oprensningsplaner med affinitetskromatografi - Google Patents

Sekventielle proteinisolerings- og oprensningsplaner med affinitetskromatografi Download PDF

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Publication number
DK1786273T3
DK1786273T3 DK05791084.6T DK05791084T DK1786273T3 DK 1786273 T3 DK1786273 T3 DK 1786273T3 DK 05791084 T DK05791084 T DK 05791084T DK 1786273 T3 DK1786273 T3 DK 1786273T3
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DK
Denmark
Prior art keywords
plasma
ligand
ligands
protein
column
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DK05791084.6T
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English (en)
Inventor
Steven James Burton
Baldev Baines
John Curling
Dwun-Hou Chen
Christopher Bryant
David John Hammond
Timothy Keith Hayes
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Prometic Biosciences Ltd
The American Nat Red Cross
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Publication of DK1786273T3 publication Critical patent/DK1786273T3/da

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K14/00Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/745Blood coagulation or fibrinolysis factors
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K1/00General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
    • C07K1/14Extraction; Separation; Purification
    • C07K1/16Extraction; Separation; Purification by chromatography
    • C07K1/22Affinity chromatography or related techniques based upon selective absorption processes
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K14/00Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/775Apolipopeptides

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Biophysics (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Medicinal Chemistry (AREA)
  • Molecular Biology (AREA)
  • Biochemistry (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Toxicology (AREA)
  • Zoology (AREA)
  • Analytical Chemistry (AREA)
  • Hematology (AREA)
  • Peptides Or Proteins (AREA)
  • Treatment Of Liquids With Adsorbents In General (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)

Claims (14)

1. Fremgangsmåde til sekventiel proteinisolering og oprensning omfattende (i) tilvejebringelse af en plasmaprøve, (ii) tilvejebringelse af ligander, som hver især binder specifikt til et målprotein i den biologiske prøve, hvori hver af liganderne valgfrit knyttes til et underlag for at danne ligand-underlagskomplekser, (iii) at liganderne eller ligandunderlagskomplekserne sekventielt og i en forudbestemt rækkefølge bringes i kontakt med plasmaprøven for at gøre det muligt for hver enkelt ligand eller ligandunderlagskompleks sekventielt at binde målproteinet fra plasmaprøven, hvori den forudbestemte rækkefølge, i hvilken liganderne eller ligand-underlagskomplekserne bringes i kontakt med plasmaprøven, resulterer i binding af plasminogen før IgG og IgG før albumin, og hvori den biologiske prøve ikke behandles ved hjælp af et forbehandlingstrin valgt fra gruppen bestående af alkoholudfældning, cryoudfældning, fjernelse af lipider og/eller lipidproteiner, euglobulinudfældning eller en kombination deraf, forud for kontakten, (iv) eluering af målproteinet bundet til hver af liganderne eller ligand-underlagskomplekserne og (v) sekventiel isolering af målproteinet fra den biologiske prøve.
2. Fremgangsmåde ifølge krav 1, hvori målproteinerne omfatter fibrinogen, alpha-1 proteinaseinhibitor, apolipoprotein A1, immunglobuliner, paraoxonase, koagulationsfaktorer, vWF/FVIll, albumin, plasminogen eller en kombination deraf.
3. Fremgangsmåde ifølge krav 2, hvori fibrinogen isoleres fra plasma før IgG.
4. Fremgangsmåde ifølge krav 2, hvori aktiviteten af paraoxonase bibeholdes i den biologiske prøve under proteinisoleringen.
5. Fremgangsmåde ifølge krav 2, hvori vWF/FVIll isoleres fra plasma forud for plasminogen.
6. Fremgangsmåde ifølge krav 2, hvori apolipoprotein A1 isoleres fra plasma før IgG.
7. Fremgangsmåde ifølge krav 2, hvori alpha-1 proteinaseinhibitor isoleres fra plasma efter albumin.
8. Fremgangsmåde ifølge krav 2, hvori plasminogen isoleres fra plasma forud for fibrinogen.
9. Fremgangsmåde ifølge krav 1, hvori liganden omfatter et peptid, polypeptid, peptidefterlignende stof, lille molekyle, farvestof, en triazinholdig forbindelse, et antistofeller antigenbindende fragment, nukleinsyre-baseret molekyle, non-polypeptid- eller nukleotid-baseret molekyle, kulhydrat, kulhydratefterlignende stoffer, lipider, uorganisk materiale, inhibitor, substrat eller enhver kombination deraf.
10. Fremgangsmåde ifølge krav 9, hvori liganderne omfatter peptider bestående af 3 til 5, 8, 10 eller 15 aminosyrer.
11. Fremgangsmåde ifølge krav 1, hvori underlaget omfatter et syntetisk materiale, et naturligt materiale eller begge.
12. Fremgangsmåde ifølge krav 1, hvori underlaget omfatter agarose, polyacrylamid, dextran, cellulose, polysaccharid, nitrocellulose, silica, alumina, aluminumoxid, titania, titaniumoxid, zirconia, styren, polyvinyldifluorid nylon, copolymer af styren og divinylbenzen, polymethacrylatester, derivatiseret azlactonpolymer eller -copolymer, glass, cellulose, agarose, derivater af enhver af de foregående og kombinationer af enhver af de foregående.
13. Fremgangsmåde ifølge krav 1, hvori underlaget er en harpiksperle.
14. Fremgangsmåde ifølge krav 1, hvori plasmaprøven behandles med et buffermiddel forud for kontakttrinnet med henblik på yderligere at konservere koncentrationen og aktiviteten af et eller flere målmidler i plasmaprøven.
DK05791084.6T 2004-08-20 2005-08-19 Sekventielle proteinisolerings- og oprensningsplaner med affinitetskromatografi DK1786273T3 (da)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US60286804P 2004-08-20 2004-08-20
PCT/US2005/029739 WO2006023831A2 (en) 2004-08-20 2005-08-19 Sequential protein isolation and purification schemes by affinity chromatography

Publications (1)

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DK1786273T3 true DK1786273T3 (da) 2019-02-18

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US (1) US8198407B1 (da)
EP (1) EP1786273B1 (da)
JP (1) JP4970260B2 (da)
CN (1) CN101035439B (da)
AU (1) AU2005277190B2 (da)
BR (1) BRPI0514435B8 (da)
CA (1) CA2576963C (da)
DK (1) DK1786273T3 (da)
ES (1) ES2710025T3 (da)
MX (1) MX2007002085A (da)
MY (1) MY147996A (da)
PL (1) PL1786273T3 (da)
PT (1) PT1786273T (da)
TW (1) TWI392685B (da)
WO (1) WO2006023831A2 (da)

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Publication number Publication date
CA2576963C (en) 2015-02-17
TWI392685B (zh) 2013-04-11
JP2008510724A (ja) 2008-04-10
EP1786273B1 (en) 2018-11-14
TW200621798A (en) 2006-07-01
BRPI0514435B8 (pt) 2021-05-25
EP1786273A2 (en) 2007-05-23
BRPI0514435B1 (pt) 2019-08-13
ES2710025T3 (es) 2019-04-22
CN101035439A (zh) 2007-09-12
WO2006023831A3 (en) 2006-06-08
AU2005277190A1 (en) 2006-03-02
BRPI0514435A (pt) 2008-06-10
US8198407B1 (en) 2012-06-12
PL1786273T3 (pl) 2019-05-31
WO2006023831A2 (en) 2006-03-02
JP4970260B2 (ja) 2012-07-04
MX2007002085A (es) 2007-07-19
EP1786273A4 (en) 2010-05-26
AU2005277190B2 (en) 2011-03-03
CN101035439B (zh) 2013-02-06
PT1786273T (pt) 2019-02-19
MY147996A (en) 2013-02-28
CA2576963A1 (en) 2006-03-02

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