Selective Modulation of Dynamic Protein Complexes

Cell Chem Biol. 2020 Aug 20;27(8):986-997. doi: 10.1016/j.chembiol.2020.07.019. Epub 2020 Aug 11.

Abstract

Dynamic proteins perform critical roles in cellular machines, including those that control proteostasis, transcription, translation, and signaling. Thus, dynamic proteins are prime candidates for chemical probe and drug discovery but difficult targets because they do not conform to classical rules of design and screening. Selectivity is pivotal for candidate probe molecules due to the extensive interaction network of these dynamic hubs. Recognition that the traditional rules of probe discovery are not necessarily applicable to dynamic proteins and their complexes, as well as technological advances in screening, have produced remarkable results in the last 2-4 years. Particularly notable are the improvements in target selectivity for small-molecule modulators of dynamic proteins, especially with techniques that increase the discovery likelihood of allosteric regulatory mechanisms. We focus on approaches to small-molecule screening that appear to be more suitable for highly dynamic targets and have the potential to streamline identification of selective modulators.

Keywords: drug discovery; dynamic proteins; probe discovery; protein-protein interactions.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Allosteric Regulation
  • CREB-Binding Protein / metabolism
  • HSP70 Heat-Shock Proteins / chemistry
  • HSP70 Heat-Shock Proteins / metabolism
  • Models, Molecular
  • Molecular Probes / chemistry
  • Molecular Probes / metabolism
  • Protein Binding
  • Proteins / chemistry
  • Proteins / metabolism*
  • Small Molecule Libraries / chemistry
  • Small Molecule Libraries / metabolism

Substances

  • HSP70 Heat-Shock Proteins
  • Molecular Probes
  • Proteins
  • Small Molecule Libraries
  • CREB-Binding Protein