The chemical biology of apoptosis. Exploring protein-protein interactions and the life and death of cells with small molecules

Chem Biol. 2002 Oct;9(10):1059-72. doi: 10.1016/s1074-5521(02)00247-8.

Abstract

Apoptosis, a fundamental process for both human health and disease, is initiated and regulated by protein-protein interactions, notable examples of which are the interactions involving Bcl-2 and IAP protein families. This article discusses recent advances in the use of chemical approaches in discovering and studying small molecules targeted to proteins of the Bcl-2 and IAP families. These small molecules and their complexes with receptors provide the tools and model systems to probe the basic mechanism of molecule recognition underling the life and death of cells and develop novel strategies for therapeutic intervention of the dysregulated apoptotic process. The review of these studies highlights the opportunity and challenge in this emerging area of chemical and chemical biological research.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Apoptosis / physiology*
  • Binding Sites
  • Caspase Inhibitors
  • Caspases / metabolism
  • Cell Survival / physiology
  • Humans
  • Ligands
  • Mitochondria / physiology
  • Models, Biological
  • Models, Molecular
  • Molecular Sequence Data
  • Protein Binding
  • Protein Structure, Tertiary
  • Proto-Oncogene Proteins c-bcl-2 / antagonists & inhibitors
  • Proto-Oncogene Proteins c-bcl-2 / genetics
  • Proto-Oncogene Proteins c-bcl-2 / physiology*
  • Sequence Alignment

Substances

  • Caspase Inhibitors
  • Ligands
  • Proto-Oncogene Proteins c-bcl-2
  • Caspases