From Atomic Structures to Neuronal Functions of G Protein-Coupled Receptors

被引:33
|
作者
Palczewski, Krzysztof [1 ]
Orban, Tivadar [1 ]
机构
[1] Case Western Reserve Univ, Sch Med, Dept Pharmacol, Cleveland, OH 44106 USA
来源
关键词
GPCRs; signal transduction; membrane biology; transmembrane receptors; receptor pharmacology; allosteric regulation; rhodopsin; crystal structure; CYCLIC ADENINE RIBONUCLEOTIDE; INTERNAL WATER-MOLECULES; CRYSTAL-STRUCTURE; HETEROLOGOUS EXPRESSION; OPIOID RECEPTOR; ADENOSINE 3,5-PHOSPHATE; CONFORMATIONAL-CHANGES; ACTIVATION MECHANISM; SIGNAL-TRANSDUCTION; GPCR OLIGOMERS;
D O I
10.1146/annurev-neuro-062012-170313
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
G protein-coupled receptors (GPCRs) are essential mediators of signal transduction, neurotransmission, ion channel regulation, and other cellular events. GPCRs are activated by diverse stimuli, including light, enzymatic processing of their N-termini, and binding of proteins, peptides, or small molecules such as neurotransmitters. GPCR dysfunction caused by receptor mutations and environmental challenges contributes to many neurological diseases. Moreover, modern genetic technology has helped identify a rich array of mono- and multigenic defects in humans and animal models that connect such receptor dysfunction with disease affecting neuronal function. The visual system is especially suited to investigate GPCR structure and function because advanced imaging techniques permit structural studies of photoreceptor neurons at both macro and molecular levels that, together with biochemical and physiological assessment in animal models, provide a more complete understanding of GPCR signaling.
引用
收藏
页码:139 / 164
页数:26
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