Structure of a human synaptic GABAA receptor

被引:434
作者
Zhu, Shaotong [1 ,2 ]
Noviello, Colleen M. [1 ,2 ]
Teng, Jinfeng [1 ,2 ]
Walsh, Richard M., Jr. [1 ,2 ]
Kim, Jeong Joo [1 ,2 ]
Hibbs, Ryan E. [1 ,2 ]
机构
[1] Univ Texas Southwestern Med Ctr Dallas, Dept Neurosci, Dallas, TX 75390 USA
[2] Univ Texas Southwestern Med Ctr Dallas, Dept Biophys, Dallas, TX 75390 USA
关键词
AMINOBUTYRIC ACID(A) RECEPTOR; BENZODIAZEPINE BINDING-SITE; GAMMA-SUBUNIT; BETA-SUBUNIT; A RECEPTORS; AGONIST; MODULATION; PHARMACOLOGY; INSIGHTS; AFFINITY;
D O I
10.1038/s41586-018-0255-3
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Fast inhibitory neurotransmission in the brain is principally mediated by the neurotransmitter GABA (gamma-aminobutyric acid) and its synaptic target, the type A GABA receptor (GABA(A) receptor). Dysfunction of this receptor results in neurological disorders and mental illnesses including epilepsy, anxiety and insomnia. The GABA(A) receptor is also a prolific target for therapeutic, illicit and recreational drugs, including benzodiazepines, barbiturates, anaesthetics and ethanol. Here we present high-resolution cryo-electron microscopy structures of the human alpha 1 beta 2 gamma 2 GABA(A) receptor, the predominant isoform in the adult brain, in complex with GABA and the benzodiazepine site antagonist flumazenil, the first-line clinical treatment for benzodiazepine overdose. The receptor architecture reveals unique heteromeric interactions for this important class of inhibitory neurotransmitter receptor. This work provides a template for understanding receptor modulation by GABA and benzodiazepines, and will assist rational approaches to therapeutic targeting of this receptor for neurological disorders and mental illness.
引用
收藏
页码:67 / +
页数:22
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