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Predicting serpin/protease interactions.
- 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.)
- Subjects :
- Amino Acid Sequence
Animals
Base Sequence
Binding Sites
Humans
Models, Molecular
Molecular Sequence Data
Protein Binding drug effects
Protein Interaction Domains and Motifs drug effects
Protein Structure, Secondary drug effects
Proteome chemistry
Proteome genetics
Serpins chemistry
Serpins pharmacology
Substrate Specificity
Computational Biology methods
Granzymes metabolism
Peptide Library
Proteolysis drug effects
Proteome metabolism
Serpins metabolism
Subjects
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