Shichida Y, Imai H
Department of Biophysics, Graduate School of Science, Kyoto University, Japan.
Cell Mol Life Sci. 1998 Dec;54(12):1299-315. doi: 10.1007/s000180050256.
The visual pigment present in photoreceptor cells is a prototypical G-protein-coupled receptor (GPCR) that receives a light signal from the outer environment using a light-absorbing chromophore, 11-cis-retinal. Through cis-trans isomerization of the chromophore, light energy is transduced into chemical free energy, which is in turn utilized for conformational changes in the protein to activate the retinal G-protein. In combination with site-directed mutagenesis, various spectroscopic and biochemical studies identified functional residues responsible for chromophore binding, color regulation, intramolecular signal transduction and G-protein coupling. Extensive studies reveal that these residues are localized into specific domains of visual pigments, suggesting a highly manipulated molecular architecture in visual pigments. In addition to the recent findings on dysfunctional mutations in patients with retinitis pigmentosa or congenital night blindness, the mechanism of intramolecular signal transduction in visual pigments and their evolutionary relationship are discussed.
光感受器细胞中存在的视觉色素是一种典型的G蛋白偶联受体(GPCR),它利用吸光发色团11-顺式视黄醛从外部环境接收光信号。通过发色团的顺反异构化,光能被转化为化学自由能,进而用于蛋白质的构象变化以激活视网膜G蛋白。结合定点诱变,各种光谱学和生物化学研究确定了负责发色团结合、颜色调节、分子内信号转导和G蛋白偶联的功能残基。广泛的研究表明,这些残基定位于视觉色素的特定结构域,这表明视觉色素中存在高度精细的分子结构。除了最近关于色素性视网膜炎或先天性夜盲症患者功能失调突变的发现外,还讨论了视觉色素分子内信号转导的机制及其进化关系。