Abstract

A two-dimensional mapping method developed for collagen chains has been applied to the CNBr-peptides of rat collagen types I, II and III and bovine type V (AB) collagen. The method consists of isoelectric focusing in a 4% polyacrylamide gel-6 M urea-2% Pharmalyte with a pH gradient ranging 5 to 10 in the first dimension and SDS-polyacrylamide slab gel (15%) electrophoresis at pH 8.8 in the second dimension. Characteristic peptide maps were obtained for each type of α-chain and can be used for identification of isolated collagen chains. Application of this method to an authentic mixture of collagen types and a fraction isolated from rat skin has indicated that the method is sensitive enough to resolve collagen types with a sample as low as 40 μg per α-chain.

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