Literature DB >> 26826315

Fibulin-1 purification from human plasma using affinity chromatography on Factor H-Sepharose.

Richard G DiScipio1, Robert C Liddington2, Ingrid U Schraufstatter3.   

Abstract

A method is reported to purify Fibulin-1 from human plasma resulting in a 36% recovery. The steps involve removal of the cryoglobulin and the vitamin K dependent proteins followed by polyethylene glycol and ammonium sulfate precipitations, DEAE-Sephadex column chromatography and finally Factor H-Sepharose affinity purification. The procedure is designed to be integrated into an overall scheme for the isolation of over 30 plasma proteins from a single batch of human plasma. Results from mass spectroscopy, SDS-PAGE, and Western blotting indicate that human plasma Fibulin-1 is a single chain of the largest isotype. Functional binding assays demonstrated calcium ion dependent interaction of Fibulin-1 for fibrinogen, fibronectin, and Factor H. The procedure described is the first to our knowledge that enables a large scale purification of Fibulin-1 from human plasma.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Affinity chromatography; Complement Factor H; Fibulin-1; Human plasma; Purification

Mesh:

Substances:

Year:  2016        PMID: 26826315      PMCID: PMC4803571          DOI: 10.1016/j.pep.2016.01.013

Source DB:  PubMed          Journal:  Protein Expr Purif        ISSN: 1046-5928            Impact factor:   1.650


  60 in total

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8.  Isolation o human fibrinogen of high purity and in high yield using polyethylene glycol 1000.

Authors:  M A Masri; S A Masri; N D Boyd
Journal:  Thromb Haemost       Date:  1983-04-28       Impact factor: 5.249

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10.  Purification and characterization of TAFI, a thrombin-activable fibrinolysis inhibitor.

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