Why Do Disordered and Structured Proteins Behave Differently in Phase Separation?

Trends Biochem Sci. 2018 Jul;43(7):499-516. doi: 10.1016/j.tibs.2018.03.007. Epub 2018 Apr 30.

Abstract

Intracellular membraneless organelles and their myriad cellular functions have garnered tremendous recent interest. It is becoming well accepted that they form via liquid-liquid phase separation (LLPS) of protein mixtures (often including RNA), where the organelles correspond to a protein-rich droplet phase coexisting with a protein-poor bulk phase. The major protein components contain disordered regions and often also RNA-binding domains, and the disordered fragments on their own easily undergo LLPS. By contrast, LLPS for structured proteins has been observed infrequently. The contrasting phase behaviors can be explained by modeling disordered and structured proteins, respectively, as polymers and colloids. These physical models also provide a better understanding of the regulation of droplet formation by cellular signals and its dysregulation leading to diseases.

Keywords: membraneless organelle; phase separation; transient bonding network.

Publication types

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

MeSH terms

  • Amino Acid Motifs
  • Animals
  • Humans
  • Hydrophobic and Hydrophilic Interactions
  • Intrinsically Disordered Proteins / chemistry
  • Intrinsically Disordered Proteins / metabolism*
  • Kinetics
  • Models, Molecular*
  • Protein Interaction Domains and Motifs
  • Protein Stability
  • Proteins / chemistry
  • Proteins / metabolism*
  • RNA, Messenger / chemistry
  • RNA, Messenger / metabolism
  • Solubility

Substances

  • Intrinsically Disordered Proteins
  • Proteins
  • RNA, Messenger