Identification of novel direct protein-protein interactions by irradiating living cells with femtosecond UV laser pulses

Biochem Biophys Res Commun. 2017 Oct 7;492(1):67-73. doi: 10.1016/j.bbrc.2017.08.037. Epub 2017 Aug 12.

Abstract

The identification of protein-protein interaction networks in living cells is becoming increasingly fundamental to elucidate main biological processes and to understand disease molecular bases on a system-wide level. We recently described a method (LUCK, Laser UV Cross-linKing) to cross-link interacting protein surfaces in living cells by UV laser irradiation. By using this innovative methodology, that does not require any protein modification or cell engineering, here we demonstrate that, upon UV laser irradiation of HeLa cells, a direct interaction between GAPDH and alpha-enolase was "frozen" by a cross-linking event. We validated the occurrence of this direct interaction by co-immunoprecipitation and Immuno-FRET analyses. This represents a proof of principle of the LUCK capability to reveal direct protein interactions in their physiological environment.

Keywords: Living cells irradiation; Metabolic nanomachines; Protein-protein interactions; UV cross-linking; Ultrashort UV laser pulses.

Publication types

  • Validation Study

MeSH terms

  • Fluorescence Resonance Energy Transfer
  • Glyceraldehyde 3-Phosphate Dehydrogenase (NADP+) / chemistry*
  • Glyceraldehyde 3-Phosphate Dehydrogenase (NADP+) / metabolism
  • HeLa Cells
  • Humans
  • Immunoprecipitation
  • Lasers*
  • Mass Spectrometry
  • Molecular Docking Simulation
  • Phosphopyruvate Hydratase / chemistry*
  • Phosphopyruvate Hydratase / metabolism
  • Protein Binding / radiation effects
  • Protein Interaction Mapping / methods*
  • Protein Interaction Maps / radiation effects*
  • Time Factors
  • Ultraviolet Rays*

Substances

  • Glyceraldehyde 3-Phosphate Dehydrogenase (NADP+)
  • Phosphopyruvate Hydratase