Affinity-driven peptide selection of an NFAT inhibitor more selective than cyclosporin A

Science. 1999 Sep 24;285(5436):2129-33. doi: 10.1126/science.285.5436.2129.

Abstract

The flow of information from calcium-mobilizing receptors to nuclear factor of activated T cells (NFAT)-dependent genes is critically dependent on interaction between the phosphatase calcineurin and the transcription factor NFAT. A high-affinity calcineurin-binding peptide was selected from combinatorial peptide libraries based on the calcineurin docking motif of NFAT. This peptide potently inhibited NFAT activation and NFAT-dependent expression of endogenous cytokine genes in T cells, without affecting the expression of other cytokines that require calcineurin but not NFAT. Substitution of the optimized peptide sequence into the natural calcineurin docking site increased the calcineurin responsiveness of NFAT. Compounds that interfere selectively with the calcineurin-NFAT interaction without affecting calcineurin phosphatase activity may be useful as therapeutic agents that are less toxic than current drugs.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Binding Sites
  • Calcineurin / metabolism*
  • Calcineurin Inhibitors
  • Cell Nucleus / metabolism
  • Cyclosporine / pharmacology
  • Cytokines / biosynthesis
  • Cytokines / genetics
  • DNA-Binding Proteins / antagonists & inhibitors*
  • DNA-Binding Proteins / chemistry
  • DNA-Binding Proteins / metabolism
  • Gene Expression Regulation
  • Genes, Reporter
  • HeLa Cells
  • Humans
  • Immunosuppressive Agents / chemistry
  • Immunosuppressive Agents / metabolism
  • Immunosuppressive Agents / pharmacology*
  • Jurkat Cells
  • Molecular Sequence Data
  • NFATC Transcription Factors
  • Nuclear Proteins*
  • Oligopeptides / chemistry
  • Oligopeptides / metabolism
  • Oligopeptides / pharmacology*
  • Peptide Library
  • Peptides / chemistry
  • Peptides / metabolism
  • Peptides / pharmacology*
  • Phosphorylation
  • Recombinant Fusion Proteins / metabolism
  • T-Lymphocytes / drug effects*
  • T-Lymphocytes / immunology
  • Transcription Factors / antagonists & inhibitors*
  • Transcription Factors / chemistry
  • Transcription Factors / metabolism
  • Transfection

Substances

  • Calcineurin Inhibitors
  • Cytokines
  • DNA-Binding Proteins
  • Immunosuppressive Agents
  • NFATC Transcription Factors
  • Nuclear Proteins
  • Oligopeptides
  • Peptide Library
  • Peptides
  • Recombinant Fusion Proteins
  • Transcription Factors
  • VIVIT peptide
  • Cyclosporine
  • Calcineurin