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Purification of cathepsin B by a new form of affinity chromatography.

Abstract
Human cathepsin B was purified by affinity chromatography on the semicarbazone of Gly-Phe-glycinal linked to Sepharose 4B, with elution by 2,2'-dipyridyl disulphide at pH 4.0. The product obtained in high yield by the single step from crude starting material was 80-100% active cathepsin B. The possibility that this new form of affinity chromatography may be of general usefulness in the purification of cysteine proteinases is discussed.

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Repository PubMed Central (PMC3 - NLM DTD) (United States)
Keywords Research Article
Type Text
Language Englisch