Novel Structural Insights into GPCR-β-Arrestin Interaction and Signaling

Trends Cell Biol. 2017 Nov;27(11):851-862. doi: 10.1016/j.tcb.2017.05.008. Epub 2017 Jun 23.

Abstract

G protein-coupled receptors (GPCRs) are major signal recognition and transmission units in the plasma membrane. The interaction of activated and phosphorylated GPCRs with the multifunctional adaptor proteins β-arrestins (βarrs) is crucial for regulation of their signaling and functional outcomes. Over the past few years, a range of structural, biochemical, and cellular studies have revealed novel insights into GPCR-βarr interaction and signaling. Some of these findings have come as a surprise and therefore have the potential to significantly refine the conceptual framework of the GPCR-βarr system. Here we discuss these recent advances with particular emphasis on biphasic GPCR-βarr interaction, the formation of GPCR-G-protein-βarr supercomplexes, and receptor-specific conformational signatures in βarrs. We also underline the emerging research areas that are likely to be at the center stage of investigations in the coming years.

Keywords: GPCRs; biased agonism; cellular signaling; desensitization; endocytosis; β-arrestins.

Publication types

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

MeSH terms

  • Animals
  • Cell Membrane / metabolism*
  • Endocytosis
  • Endosomes / metabolism
  • Humans
  • Phosphorylation
  • Protein Binding
  • Receptors, G-Protein-Coupled / metabolism*
  • Signal Transduction*
  • beta-Arrestins / metabolism*

Substances

  • Receptors, G-Protein-Coupled
  • beta-Arrestins