Mass spectrometry methods to study protein-metabolite interactions

Expert Opin Drug Discov. 2017 Dec;12(12):1271-1280. doi: 10.1080/17460441.2017.1378178. Epub 2017 Sep 21.

Abstract

To ​​​​understand and manipulate biochemical processes and signaling pathways, the knowledge of endogenous protein-metabolite interactions would be extremely helpful. Recent developments in precision mass spectrometry, high-throughput proteomics and sensitive metabolomic profiling are beginning to converge on a possible solution, heralding a new era of global metabolome-proteome 'interactome' studies that promise to change biomedical research and drug discovery. Areas covered: Here, we review innovative mass spectrometry-based methods and recent pioneering studies aimed at elucidating the physical associations of small molecule ligands with cellular proteins. The technologies covered belong to two main categories: tag-based and tag-free methods. We emphasize the latter in this review, and outline promising experimental workflows and key data analysis considerations involved. Expert opinion: Recent ground-breaking advances in chemical-proteomics technology and allied computational methods now make the global detection of protein-ligand engagement an increasingly attractive research problem. Despite ongoing challenges, rapid progress in the field is expected these coming next few years, leading to a refreshed systems biology research paradigm and much needed new opportunities for improving sparse drug discovery pipelines.

Keywords: Protein-metabolite interaction; mass spectrometry; metabolomics; proteomics.

Publication types

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

MeSH terms

  • Biomedical Research / methods
  • Drug Discovery / methods*
  • High-Throughput Screening Assays
  • Humans
  • Ligands
  • Mass Spectrometry / methods*
  • Metabolome / physiology
  • Metabolomics / methods
  • Proteins / metabolism*
  • Proteome / metabolism
  • Proteomics / methods
  • Systems Biology / methods

Substances

  • Ligands
  • Proteins
  • Proteome