Literature DB >> 9792510

Peptide affinity chromatography of human clotting factor VIII. Screening of the vWF-binding domain.

R Necina1, K Amatschek, E Schallaun, H Schwinn, D Josic, A Jungbauer.   

Abstract

The region of von Willebrand factor, which is involved in the complex formation with factor VIII, was used to generate a panel of octapeptides. A peptide ladder was generated from the von Willebrand factor region aa40 to aa100 and was synthesized on cellulose membranes by spot technology. Four peptides with affinity for factor VIII were identified by incubation with plasma derived factor VIII and recombinant factor VIII. The peptides denoted as 010 (LCPPGMVRHE), 011 (RCPCFHQGK), 014 (CFHQGKEYA) and 015 (RDRKWNCTDHVC) were further characterized by real-time interaction analysis and small scale affinity chromatography. Biotinylated peptides were used for blotting assays. These experiments showed that the peptides are directed against the light chain of FVIII. We consider these peptides as valuable tools for in situ labeling and also as ligands suitable for affinity chromatography.

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Year:  1998        PMID: 9792510     DOI: 10.1016/s0378-4347(98)00337-5

Source DB:  PubMed          Journal:  J Chromatogr B Biomed Sci Appl        ISSN: 1387-2273


  2 in total

1.  A von Willebrand factor fragment containing the D'D3 domains is sufficient to stabilize coagulation factor VIII in mice.

Authors:  Andrew Yee; Robert D Gildersleeve; Shufang Gu; Colin A Kretz; Beth M McGee; Keisha M Carr; Steven W Pipe; David Ginsburg
Journal:  Blood       Date:  2014-05-21       Impact factor: 22.113

2.  Downstream Processing: From Egg to Cell Culture-Derived Influenza Virus Particles.

Authors:  M W Wolff; U Reichl
Journal:  Chem Eng Technol       Date:  2008-05-27       Impact factor: 1.728

  2 in total

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