Literature DB >> 10036175

Protease and protease inhibitor assays using biotinylated casein coated on a solid phase.

Z Gan1, R R Marquardt, H Xiao.   

Abstract

A new type of solid-phase assay for proteases and protease inhibitors has been developed using biotinylated casein. The assay involves coating of titer plate wells with biotinylated casein, hydrolysis of this substrate with a protease such as trypsin, reaction of the biotin from the unhydrolyzed substrate with an alkaline phosphatase-streptavidin complex, and finally quantification of the amount of casein remaining on the plate using alkaline phosphatase activity as the indicator. The activity of the bound indicator enzyme is oppositely related to the protease activity of the sample. In addition, the assay can be modified for quantitating the corresponding amount of protease inhibitor in the sample. The assay is simple, sensitive, accurate, inexpensive, and amenable to automation. Copyright 1999 Academic Press.

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Year:  1999        PMID: 10036175     DOI: 10.1006/abio.1998.3053

Source DB:  PubMed          Journal:  Anal Biochem        ISSN: 0003-2697            Impact factor:   3.365


  1 in total

1.  Integrating structure, bioinformatics, and enzymology to discover function: BioH, a new carboxylesterase from Escherichia coli.

Authors:  Ruslan Sanishvili; Alexander F Yakunin; Roman A Laskowski; Tatiana Skarina; Elena Evdokimova; Amanda Doherty-Kirby; Gilles A Lajoie; Janet M Thornton; Cheryl H Arrowsmith; Alexei Savchenko; Andrzej Joachimiak; Aled M Edwards
Journal:  J Biol Chem       Date:  2003-05-05       Impact factor: 5.157

  1 in total

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