Looking at the proteases from a simple perspective

J Mol Recognit. 2011 Mar-Apr;24(2):165-81. doi: 10.1002/jmr.1091.

Abstract

Proteases have received enormous interest from the research and medical communities because of their significant roles in several human diseases. Some examples include the involvement of thrombin in thrombosis, HIV-1 protease in Acquired Immune Deficiency Syndrome, cruzain in Trypanosoma cruzi infection, and membrane-type 1 matrix metalloproteinase in tumor invasion and metastasis. Many efforts has been undertaken to design effective inhibitors featuring potent inhibitory activity, specificity, and metabolic stability to those proteases involved in such pathologies. Protease inhibitors usually target the active site, but some of them act by other inhibitory mechanisms. The understanding of the structure-function relationships of proteases and inhibitors has an impact on new inhibitor drugs designing. In this paper, the structures of four proteases (thrombin, HIV-protease, cruzain, and a matrix metalloproteinase) are briefly reviewed, and used as examples of the importance of proteases for the development of new treatment strategies, leading to a longer and healthier life.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Cysteine Endopeptidases / chemistry
  • Cysteine Endopeptidases / metabolism
  • HIV Protease / chemistry
  • HIV Protease / metabolism
  • Humans
  • Matrix Metalloproteinases / chemistry
  • Matrix Metalloproteinases / metabolism
  • Peptide Hydrolases / chemistry
  • Peptide Hydrolases / metabolism*
  • Serine Proteases / chemistry
  • Serine Proteases / metabolism

Substances

  • Peptide Hydrolases
  • Serine Proteases
  • Cysteine Endopeptidases
  • HIV Protease
  • Matrix Metalloproteinases