High-precision mapping of protein protein interfaces: an integrated genetic strategy combining en masse mutagenesis and DNA-level parallel analysis on a yeast two-hybrid platform.

Research output: Contribution to journalArticle

Abstract

Understanding networks of protein-protein interactions constitutes an essential component on a path towards comprehensive description of cell function. Whereas efficient techniques are readily available for the initial identification of interacting protein partners, practical strategies are lacking for the subsequent high-resolution mapping of regions involved in protein-protein interfaces. We present here a genetic strategy to accurately map interacting protein regions at amino acid precision. The system is based on parallel construction, sampling and analysis of a comprehensive insertion mutant library. The methodology integrates Mu in vitro transposition-based random pentapeptide mutagenesis of proteins, yeast two-hybrid screening and high-resolution genetic footprinting. The strategy is general and applicable to any interacting protein pair. We demonstrate the feasibility of the methodology by mapping the region in human JFC1 that interacts with Rab8A, and we show that the association is mediated by the Slp homology domain 1.

Details

Authors
  • Maria Pajunen
  • Hilkka Turakainen
  • Eini Poussu
  • Johan Peränen
  • Mauno Vihinen
  • Harri Savilahti
External organisations
  • External Organization - Unknown
Research areas and keywords

Subject classification (UKÄ) – MANDATORY

  • Medical Genetics

Keywords

  • Saccharomyces cerevisiae: genetics, Insertional: methods, Mutagenesis, Membrane Proteins: metabolism, Membrane Proteins: chemistry, Membrane Proteins: genetics, rab GTP-Binding Proteins: chemistry, rab GTP-Binding Proteins: metabolism
Original languageEnglish
Pages (from-to)e103
JournalNucleic Acids Research
Volume35
Issue number16
StatePublished - 2007
Peer-reviewedYes
Externally publishedYes