明视
视蛋白
视紫红质
彩色视觉
生物
基础(线性代数)
进化生物学
暗视
发色团
G蛋白偶联受体
感知
神经科学
折叠(DSP实现)
物理
光学
序列(生物学)
生物物理学
人工智能
视觉颜料
视觉感受
视觉光转导
沟通
显微镜
作者
Sarah L. Schmidt,Jakub Dostál,Saumik Sen,Andrej Hovan,Deborah Walter,Martin V. Appleby,Asato Kojima,Hideaki Kato,John H. Beale,Miroslav Kloz,Gebhard F. X. Schertler,Polina Isaikina
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2026-06-25
卷期号:392 (6805): eadz3624-eadz3624
标识
DOI:10.1126/science.adz3624
摘要
Photopic vision, including fast motion and color perception in daylight, is mediated by cone opsins, specialized G protein-coupled receptors (GPCRs). Despite sharing the same chromophore, the three receptor subtypes absorb light at different wavelengths of the visible spectrum. The molecular mechanisms governing their spectral properties and exceptionally rapid responses remain largely unknown. We report cryo-electron microscopy structures of the human blue-sensitive (OPN1SW) and green-sensitive (OPN1MW) cone opsins in their dark-adapted states, combined with femtosecond-resolution spectroscopy, functional assays, and advanced simulations. The data reveal distinct chromophore stabilization mechanisms across human visual opsins and specific sequence adaptations in the GPCR microswitch motifs, underlining their structural plasticity and distinct activation mechanisms. These findings delineate the molecular basis of the evolutionary refinements fulfilling the needs of vision in daylight.
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