Activation of rhodopsin: new insights from structural and biochemical studies

被引:354
|
作者
Okada, T [1 ]
Ernst, OP
Palczewski, K
Hofmann, KP
机构
[1] Univ Washington, Dept Ophthalmol, Seattle, WA 98195 USA
[2] Kyoto Univ, Grad Sch Sci, Dept Biophys, Kyoto 6068502, Japan
[3] Univ Washington, Dept Ophthalmol, Seattle, WA 98195 USA
[4] Univ Washington, Dept Pharmacol & Chem, Seattle, WA 98195 USA
[5] Humboldt Univ, Klinikum Charite, Inst Med Phys & Biophys, D-10098 Berlin, Germany
关键词
D O I
10.1016/S0968-0004(01)01799-6
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
G-protein-coupled receptors (GPCRs) are involved in a vast variety of cellular signal transduction processes from visual, taste and odor perceptions to sensing the levels of many hormones and neurotransmitters. As a result of agonist-induced conformation changes, GPCRs become activated and catalyze nucleotide exchange within the G proteins, thus detecting and amplifying the signal. GPCRs share a common heptahelical transmembrane structure as well as many conserved key residues and regions. Rhodopsins are prototypical GPCRs that detect photons in retinal photoreceptor cells and trigger a phototransduction cascade that culminates in neuronal signaling. Biophysical and biochemical studies of rhodopsin activation, and the recent crystal structure determination of bovine rhodopsin, have provided new information that enables a more complete mechanism of vertebrate rhodopsin activation to be proposed. In many aspects, rhodopsin might provide a structural and functional template for other members of the GPCR family.
引用
收藏
页码:318 / 324
页数:7
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