GIT/PIX Condensates Are Modular and Ideal for Distinct Compartmentalized Cell Signaling

Mol Cell. 2020 Sep 3;79(5):782-796.e6. doi: 10.1016/j.molcel.2020.07.004. Epub 2020 Aug 10.

Abstract

Enzymes or enzyme complexes can be concentrated in different cellular loci to modulate distinct functional processes in response to specific signals. How cells condense and compartmentalize enzyme complexes for spatiotemporally distinct cellular events is not well understood. Here we discover that specific and tight association of GIT1 and β-Pix, a pair of GTPase regulatory enzymes, leads to phase separation of the complex without additional scaffolding molecules. GIT1/β-Pix condensates are modular in nature and can be positioned at distinct cellular compartments, such as neuronal synapses, focal adhesions, and cell-cell junctions, by upstream adaptors. Guided by the structure of the GIT/PIX complex, we specifically probed the role of phase separation of the enzyme complex in cell migration and synapse formation. Our study suggests that formation of modular enzyme complex condensates via phase separation can dynamically concentrate limited quantities of enzymes to distinct cellular compartments for specific and optimal signaling.

Keywords: GIT/PIX complex; GTPase-activating protein; biological condensates; focal adhesion; guanine nucleotide exchange factor; membrane-less organelles; phase separation; synapse formation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Cycle Proteins / chemistry
  • Cell Cycle Proteins / metabolism*
  • GTPase-Activating Proteins / chemistry
  • GTPase-Activating Proteins / metabolism*
  • HEK293 Cells
  • HeLa Cells
  • Humans
  • Mice
  • Models, Molecular
  • Paxillin / metabolism
  • Protein Binding
  • Recombinant Proteins / metabolism
  • Rho Guanine Nucleotide Exchange Factors / metabolism*
  • Signal Transduction*

Substances

  • Arhgef7 protein, mouse
  • Cell Cycle Proteins
  • GTPase-Activating Proteins
  • Git1 protein, mouse
  • Paxillin
  • Recombinant Proteins
  • Rho Guanine Nucleotide Exchange Factors