Mass spectrometry-based methods for analysing the mitochondrial interactome in mammalian cells

J Biochem. 2020 Mar 1;167(3):225-231. doi: 10.1093/jb/mvz090.

Abstract

Protein-protein interactions are essential biologic processes that occur at inter- and intracellular levels. To gain insight into the various complex cellular functions of these interactions, it is necessary to assess them under physiologic conditions. Recent advances in various proteomic technologies allow to investigate protein-protein interaction networks in living cells. The combination of proximity-dependent labelling and chemical cross-linking will greatly enhance our understanding of multi-protein complexes that are difficult to prepare, such as organelle-bound membrane proteins. In this review, we describe our current understanding of mass spectrometry-based proteomics mapping methods for elucidating organelle-bound membrane protein complexes in living cells, with a focus on protein-protein interactions in mitochondrial subcellular compartments.

Keywords: BioID; XL-MS; mass spectrometry; mitochondria; proteome.

Publication types

  • Review

MeSH terms

  • Cross-Linking Reagents / chemistry
  • Humans
  • Mass Spectrometry / methods*
  • Membrane Proteins / metabolism
  • Mitochondria / metabolism*
  • Organelles / metabolism
  • Proteome / chemistry*
  • Proteome / metabolism*
  • Proteomics / methods*

Substances

  • Cross-Linking Reagents
  • Membrane Proteins
  • Proteome