Collagen (types I, II, V, IX and XI) constituting polypeptide chains and their polymers and cyanogen bromide-cleaved peptides of collagen type I and type III were investigated by means of capillary zone electrophoresis. Separations were effected in 2.5 mM sodium tetraborate buffer in less than 15 m
Electrophoresis and electroblotting of native collagens
β Scribed by John A.M. Ramshaw; Jerome A. Werkmeister
- Book ID
- 102984987
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- English
- Weight
- 793 KB
- Volume
- 168
- Category
- Article
- ISSN
- 0003-2697
No coin nor oath required. For personal study only.
β¦ Synopsis
Electrophoretic and immunoblotting techniques, while now used routinely for the biochemical characterization of many proteins, have not been used for the identification of native collagens. We present here an acidic electrophoresis system using very low percentage acrylamide gels which maintains collagen solubility and allows migration of native dermal collagens. The method gives uniform gels which can be made mechanically stable for subsequent electroblotting. The resulting nitrocellulose transfer allows immunological detection of collagens using either polyclonal or monoclonal antibodies and can be used to screen antibody specificities. The majority of murine monoclonal antibodies directed against collagen bind only to conformational epitopes on the native triple-helical collagen, and thus cannot be screened by Western blotting. This method therefore enables the electrophoretic screening of these monoclonal antibodies and provides an alternative approach for their characterization.
π SIMILAR VOLUMES