Kinetics and mechanism of G protein-coupled receptor activation.

Curr Opin Cell Biol

Institute of Pharmacology and Toxicology, University of Würzburg, 97078 Würzburg, Germany; Rudolf Virchow Center, DFG-Research Center for Experimental Biomedicine, University of Würzburg, 97078 Würzburg, Germany.

Published: April 2014

AI Article Synopsis

  • Activation of G protein-coupled receptors (GPCRs) occurs when an agonist binds to the receptor or light induces changes in retinal, leading to a conformational shift to an active state.
  • New techniques like X-ray crystallography, NMR studies, molecular simulations, and FRET are being used to study this activation process.
  • The article reviews current knowledge of GPCR activation kinetics, spanning from rapid (sub-microsecond) light or agonist activation to slower (milliseconds) signaling via soluble ligands.

Article Abstract

The activation of a G protein-coupled receptor is generally triggered by binding of an agonist to the receptor's binding pocket, or, in the case of rhodopsin, by light-induced changes of the pre-bound retinal. This is followed by a series of a conformational changes towards an active receptor conformation, which is capable of signalling to G proteins and other downstream proteins. In the past few years, a number of new techniques have been employed to analyze the kinetics of this activation process, including X-ray crystallographic three-dimensional structures of receptors in the inactive and the active states, NMR studies of labelled receptors, molecular simulations, and optical analyses with fluorescence resonance energy transfer (FRET). Here we review our current understanding of the activation process of GPCRs as well as open questions in the sequence of events ranging from (sub-)microsecond activation by light or agonist binding to millisecond activation of receptors by soluble ligands and the subsequent generation of an intracellular signal.

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Source
http://dx.doi.org/10.1016/j.ceb.2013.11.009DOI Listing

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