Format

Send to

Choose Destination
Nat Rev Neurosci. 2001 Apr;2(4):274-86.

Oligomerization of G-protein-coupled transmitter receptors.

Author information

1
Department of Biochemistry and Groupe de Recherche sur le système Nerveux Autonome, Faculté de Médecine, Université de Montréal, P.O. Box 6128, Down-Town Station, Montréal, Quebec, H3C 3J7 Canada. Michel.Bouvier@umontreal.ca

Abstract

Examples of G-protein-coupled receptors that can be biochemically detected in homo- or heteromeric complexes are emerging at an accelerated rate. Biophysical approaches have confirmed the existence of several such complexes in living cells and there is strong evidence to support the idea that dimerization is important in different aspects of receptor biogenesis and function. While the existence of G-protein-coupled-receptor homodimers raises fundamental questions about the molecular mechanisms involved in transmitter recognition and signal transduction, the formation of heterodimers raises fascinating combinatorial possibilities that could underlie an unexpected level of pharmacological diversity, and contribute to cross-talk regulation between transmission systems. Because G-protein-coupled receptors are major pharmacological targets, the existence of dimers could have important implications for the development and screening of new drugs. Here, we review the evidence supporting the existence of G-protein-coupled-receptor dimerization and discuss its functional importance.

PMID:
11283750
DOI:
10.1038/35067575
[Indexed for MEDLINE]

Supplemental Content

Full text links

Icon for Nature Publishing Group
Loading ...
Support Center