Renaturation of heterodimeric platelet-derived growth factor from inclusion bodies of recombinant Escherichia coli using size-exclusion chromatography

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autorschaft

  • Carsten Müller
  • Ursula Rinas

Externe Organisationen

  • Helmholtz-Zentrum für Infektionsforschung GmbH (HZI)
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Details

OriginalspracheEnglisch
Seiten (von - bis)203-213
Seitenumfang11
FachzeitschriftJournal of Chromatography A
Jahrgang855
Ausgabenummer1
PublikationsstatusVeröffentlicht - 3 Sept. 1999
Extern publiziertJa

Abstract

A procedure for renaturation of heterodimeric platelet-derived growth factor (PDGF-AB) from inclusion bodies of recombinant Escherichia coli using size-exclusion chromatography is described. Either prepurified or crude PDGF-AB inclusion bodies solubilized with guanidinium hydrochloride were subjected to buffer exchange from denaturing to renaturing conditions during chromatography. Renaturation of PDGF-AB involves folding of the solubilized and unfolded molecules into dimerization competent monomers during size-exclusion chromatography and subsequent dimerization of folded monomers into the biologically active heterodimeric growth factor. Optimized conditions result in an overall yield of 75% active PDGF-AB with respect to size-exclusion chromatography and subsequent dimerization. The described approach allows renaturation at high protein concentrations and circumvents aggregation which is observed when refolding is carried out by dilution. Copyright (C) 1999 Elsevier Science B.V.

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Renaturation of heterodimeric platelet-derived growth factor from inclusion bodies of recombinant Escherichia coli using size-exclusion chromatography. / Müller, Carsten; Rinas, Ursula.
in: Journal of Chromatography A, Jahrgang 855, Nr. 1, 03.09.1999, S. 203-213.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

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AU - Rinas, Ursula

PY - 1999/9/3

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N2 - A procedure for renaturation of heterodimeric platelet-derived growth factor (PDGF-AB) from inclusion bodies of recombinant Escherichia coli using size-exclusion chromatography is described. Either prepurified or crude PDGF-AB inclusion bodies solubilized with guanidinium hydrochloride were subjected to buffer exchange from denaturing to renaturing conditions during chromatography. Renaturation of PDGF-AB involves folding of the solubilized and unfolded molecules into dimerization competent monomers during size-exclusion chromatography and subsequent dimerization of folded monomers into the biologically active heterodimeric growth factor. Optimized conditions result in an overall yield of 75% active PDGF-AB with respect to size-exclusion chromatography and subsequent dimerization. The described approach allows renaturation at high protein concentrations and circumvents aggregation which is observed when refolding is carried out by dilution. Copyright (C) 1999 Elsevier Science B.V.

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