Inhibition of genotoxic stress induced apoptosis by novel TAT-fused peptides targeting PIDDosome

Biochem Pharmacol. 2012 Jan 15;83(2):218-27. doi: 10.1016/j.bcp.2011.10.013. Epub 2011 Oct 25.

Abstract

Genotoxic stress induced apoptosis is mediated by the formation of PIDDosome, which is a caspase-2 activating complex composed of three protein components, PIDD, RAIDD, and caspase-2. Here, synthetic TAT-fused peptides designed by the structure of PIDD and RAIDD, TAT-Y814A and TAT-R147E, respectively, were produced and tested for their ability to inhibit PIDDosome formation in vitro as well as to attenuate genotoxic stress-induced apoptosis in human renal cancer cells. The results show that TAT-Y814A and TAT-R147E have the potential to inhibit formation of the PIDDosome in a dose-dependent manner. Furthermore, both peptides partially inhibit genotoxic stress mediated apoptosis and activation of caspase2 and caspase3 in Caki cells. These results suggest that TAT-Y814A (also TAT-R147E) is a novel inhibitor of genotoxic stress-induced apoptosis that may serve as a prototype for anti-apoptotic drug development.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Apoptosis / genetics*
  • Cell Line, Tumor
  • DNA Damage / genetics*
  • Death Domain Receptor Signaling Adaptor Proteins / antagonists & inhibitors*
  • Death Domain Receptor Signaling Adaptor Proteins / genetics
  • Death Domain Receptor Signaling Adaptor Proteins / metabolism
  • Gene Products, tat / genetics
  • Gene Products, tat / physiology*
  • Gene Targeting / methods*
  • Humans
  • Molecular Sequence Data
  • Peptide Fragments / genetics
  • Peptide Fragments / physiology*
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism
  • Recombinant Fusion Proteins / physiology

Substances

  • Death Domain Receptor Signaling Adaptor Proteins
  • Gene Products, tat
  • PIDD1 protein, human
  • Peptide Fragments
  • Recombinant Fusion Proteins