A novel proteomic approach identifies new interaction partners for proliferating cell nuclear antigen

J Mol Biol. 2007 Oct 5;372(5):1137-48. doi: 10.1016/j.jmb.2007.06.056. Epub 2007 Jun 27.

Abstract

During DNA replication and repair, many proteins bind to and dissociate in a highly specific and ordered manner from proliferating cell nuclear antigen (PCNA). We describe a combined approach of in silico searches at the genome level and combinatorial peptide synthesis to investigate the binding properties of hundreds of short PCNA-interacting peptides (PIP-peptides) to archaeal and eukaryal PCNAs. Biological relevance of our combined approach was demonstrated by identification an inactive complex of Pyrococcus abyssi ribonuclease HII with PCNA. Furthermore we show that PIP-peptides interact with PCNA largely in a sequence independent manner. Our experimental approach also identified many so far unidentified PCNA interacting peptides in a number of human proteins.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Archaeal Proteins / genetics
  • Archaeal Proteins / metabolism
  • DNA Ligases / genetics
  • DNA Ligases / metabolism
  • DNA Repair
  • Flap Endonucleases / genetics
  • Flap Endonucleases / metabolism
  • Humans
  • Molecular Sequence Data
  • Peptides / genetics
  • Peptides / metabolism*
  • Proliferating Cell Nuclear Antigen / genetics
  • Proliferating Cell Nuclear Antigen / metabolism*
  • Proteome*
  • Pyrococcus abyssi / enzymology
  • Ribonuclease H / genetics
  • Ribonuclease H / metabolism
  • Sequence Alignment

Substances

  • Archaeal Proteins
  • Peptides
  • Proliferating Cell Nuclear Antigen
  • Proteome
  • Flap Endonucleases
  • ribonuclease HII
  • Ribonuclease H
  • DNA Ligases