期刊
PHOTOCHEMICAL & PHOTOBIOLOGICAL SCIENCES
卷 3, 期 6, 页码 628-638出版社
SPRINGERNATURE
DOI: 10.1039/b315661c
关键词
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资金
- NATIONAL EYE INSTITUTE [P30EY001730, R29EY008061, R01EY008061] Funding Source: NIH RePORTER
G protein-coupled receptors (GPCRs) are ubiquitous and essential in modulating virtually all physiological processes. These receptors share a similar structural design consisting of the seven-transmembrane alpha-helical segments. The active conformations of the receptors are stabilized by an agonist and couple to structurally highly conserved heterotrimeric G proteins. One of the most important unanswered questions is how GPCRs couple to their cognate G proteins. Phototransduction represents an excellent model system for understanding G protein signaling, owing to the high expression of rhodopsin in rod photoreceptors and the multidisciplinary experimental approaches used to study this GPCR. Here, we describe how a G protein (transducin) docks on to an oligomeric GPCR (rhodopsin), revealing structural details of this critical interface in the signal transduction process. This conceptual model takes into account recent structural information on the receptor and G protein, as well as oligomeric states of GPCRs.
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