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Skin Surface Proteolytic Activity

Partial Characterization and Identification

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Aspartic Proteinases

Part of the book series: Advances in Experimental Medicine and Biology ((AEMB,volume 436))

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Summary

Skin surface proteolytic activity in the living animal was determined by a sensitive, non-invasive methodology developed in our laboratory. A non-leaky well was constructed on the shaved back of an anesthetized guinea pig. The well contained the reaction mixture including the substrate 125I—S—carboxymethylated insulin B-chain (ICMI). The proteolytic activity was shown to be time-dependent. The activity was strongly inhibited by pepstatin A, indicating the involvement of aspartic proteinase(s) such as cathepsin D and/or E. Pretreatment of the skin with propylene glycol blocked the proteolytic activity. The present study demonstrates the presence of proteolytic activity located on skin surface using a unique, non-invasive method for in situ proteinase determination in the living animal.

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Correspondence to Uri Wormser .

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© 1998 Springer Science+Business Media New York

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Wormser, U. et al. (1998). Skin Surface Proteolytic Activity. In: James, M.N.G. (eds) Aspartic Proteinases. Advances in Experimental Medicine and Biology, vol 436. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-5373-1_29

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  • DOI: https://doi.org/10.1007/978-1-4615-5373-1_29

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-1-4613-7452-7

  • Online ISBN: 978-1-4615-5373-1

  • eBook Packages: Springer Book Archive

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