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Predicting serpin/protease interactions.

Authors :
Song J
Matthews AY
Reboul CF
Kaiserman D
Pike RN
Bird PI
Whisstock JC
Source :
Methods in enzymology [Methods Enzymol] 2011; Vol. 501, pp. 237-73.
Publication Year :
2011

Abstract

Proteases are tightly regulated by specific inhibitors, such as serpins, which are able to undergo considerable and irreversible conformational changes in order to trap their targets. There has been a considerable effort to investigate serpin structure and functions in the past few decades; however, the specific interactions between proteases and serpins remain elusive. In this chapter, we describe detailed experimental protocols to determine and characterize the extended substrate specificity of proteases based on a substrate phage display technique. We also describe how to employ a bioinformatics system to analyze the substrate specificity data obtained from this technique and predict the potential inhibitory serpin partners of a protease (in this case, the immune protease, granzyme B) in a step-by-step manner. The method described here could also be applied to other proteases for more generalized substrate specificity analysis and substrate discovery.<br /> (Copyright © 2011 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1557-7988
Volume :
501
Database :
MEDLINE
Journal :
Methods in enzymology
Publication Type :
Academic Journal
Accession number :
22078538
Full Text :
https://doi.org/10.1016/B978-0-12-385950-1.00012-2