4.7 Review

Structural biology of GABAB receptor

Journal

NEUROPHARMACOLOGY
Volume 136, Issue -, Pages 68-79

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neuropharm.2017.10.011

Keywords

GABA(B) receptor; Structure; Heterodimer; Ligand recognition; Activation; G protein-coupled receptor

Funding

  1. National Institute of Health [R01GM088454, R01GM112973]
  2. American Heart Association [SDG0835183N, 15GRNT25420002]

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Metabotropic GABA(B) receptor is a G protein-coupled receptor (GPCR) that mediates slow and prolonged inhibitory neurotransmission in the brain. It functions as a constitutive heterodimer composed of the GABA(B1) and GABA(B2) subunits. Each subunit contains three domains; the extracellular Venus flytrap module, seven-helix transmembrane region and cytoplasmic tail. In recent years, the three-dimensional structures of GABA(B) receptor extracellular and intracellular domains have been elucidated. These structures reveal the molecular basis of ligand recognition, receptor heterodimerization and receptor activation. Here we provide a brief review of the GABA(B) receptor structures, with an emphasis on describing the different ligand-bound states of the receptor. We will also compare these with the known structures of related GPCRs to shed light on the molecular mechanisms of activation and regulation in the GABAB system, as well as GPCR dimers in general. This article is part of the Special Issue Dedicated to Norman G. Bowery. (C) 2017 Elsevier Ltd. All rights reserved.

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