Predicting serpin/protease interactions

Methods Enzymol. 2011:501:237-73. doi: 10.1016/B978-0-12-385950-1.00012-2.

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Binding Sites
  • Computational Biology / methods*
  • Granzymes / metabolism*
  • Humans
  • Models, Molecular
  • Molecular Sequence Data
  • Peptide Library*
  • Protein Binding / drug effects
  • Protein Interaction Domains and Motifs / drug effects
  • Protein Structure, Secondary / drug effects
  • Proteolysis / drug effects*
  • Proteome / chemistry
  • Proteome / genetics
  • Proteome / metabolism*
  • Serpins / chemistry
  • Serpins / metabolism*
  • Serpins / pharmacology
  • Substrate Specificity

Substances

  • Peptide Library
  • Proteome
  • Serpins
  • Granzymes