Structural elements involved in activation of the γ-aminobutyric acid type A (GABAA)receptor

被引:43
作者
Kash, TL
Trudell, JR
Harrison, NL [1 ]
机构
[1] Cornell Univ, Weill Grad Sch Biomed Sci, Grad Program Neurosci, New York, NY 10021 USA
[2] Stanford Univ, Dept Anesthesia, Stanford, CA 94305 USA
[3] Stanford Univ, Beckman Program Mol & Genet Med, Stanford, CA 94305 USA
[4] Cornell Univ, Weill Med Coll, Dept Anesthesiol, New York, NY 10021 USA
[5] Cornell Univ, Weill Med Coll, Dept Pharmacol, New York, NY 10021 USA
关键词
gamma-aminobutyric acid (GABA); licand-gated ion channel (LGIC); LGIC activation; LGIC structure; modeling;
D O I
10.1042/BST0320540
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ligand-gated ion channels function as rapid signal transducers, converting chemical signals (in the form of neurotransmitters) into electrical signals in the postsynaptic neuron. This is achieved by the recognition of neurotransmitter at its specific-binding sites, which then triggers the opening of an ion channel ('gating'). For this to occur rapidly (<1 ms), there must be an efficient coupling between the agonist-binding site and the gate, located more than 30 A (11 Angstrom = 0.1 nm) away. Whereas a great deal of progress has been made in elucidating the structure and function of both the agonist-binding site and the ion permeation pathway in ligand-gated ion channels, our knowledge of the coupling mechanism between these domains has been limited. in this review, we summarize recent studies of the agonist-binding site and the ion channel in the gamma-aminobutyric acid type A receptor, and discuss those structural elements that may mediate coupling between them. We will also consider some possible molecular mechanisms of receptor activation.
引用
收藏
页码:540 / 546
页数:7
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