GPCR activation: a mutagenic spotlight on crystal structures

Trends Pharmacol Sci. 2013 Jan;34(1):67-84. doi: 10.1016/j.tips.2012.11.002. Epub 2012 Dec 13.

Abstract

The crystal structures of antagonist and agonist complexes of isolated β(2) and β(1) adrenoceptors have recently been supplemented by antagonist structures of M(2) and M(3) muscarinic acetylcholine receptors. Importantly, a structure of an agonist-ligated β(2) adrenoceptor complexed with its cognate G protein has provided the first view of a ternary complex representing the transition state in agonist-mediated G protein activation. This review interprets these G-protein-coupled receptor (GPCR) structures through the focus provided by extensive mutagenesis studies on muscarinic receptors, revealing an activation mechanism that is both modular and dynamic. Specific motifs, based around highly conserved residues, functionalise the seven-transmembrane architecture of these receptors. While exploiting conserved motifs, the ligand binding and signal transduction pathways work around and through water-containing cavities, an emerging feature of GPCR structures. These cavities may have undergone evolutionary selection to adapt GPCRs to particular signalling niches, and may provide targeting opportunities to enhance drug selectivity.

Publication types

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

MeSH terms

  • Adrenergic beta-Agonists / chemistry
  • Crystallography, X-Ray
  • Humans
  • Models, Molecular
  • Protein Conformation
  • Receptor, Muscarinic M1 / agonists
  • Receptor, Muscarinic M1 / antagonists & inhibitors
  • Receptor, Muscarinic M1 / chemistry
  • Receptor, Muscarinic M2 / agonists
  • Receptor, Muscarinic M2 / antagonists & inhibitors
  • Receptor, Muscarinic M2 / chemistry
  • Receptors, Adrenergic, beta / chemistry
  • Receptors, G-Protein-Coupled / agonists
  • Receptors, G-Protein-Coupled / antagonists & inhibitors
  • Receptors, G-Protein-Coupled / chemistry*
  • Structure-Activity Relationship

Substances

  • Adrenergic beta-Agonists
  • Receptor, Muscarinic M1
  • Receptor, Muscarinic M2
  • Receptors, Adrenergic, beta
  • Receptors, G-Protein-Coupled