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Atomistic design of microbial opsin-based blue-shifted optogenetics tools

机译:基于微生物视蛋白的蓝移光遗传学工具的原子设计

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摘要

Microbial opsins with a bound chromophore function as photosensitive ion transporters and have been employed in optogenetics for the optical control of neuronal activity. Molecular engineering has been utilized to create colour variants for the functional augmentation of optogenetics tools, but was limited by the complexity of the protein-chromophore interactions. Here we report the development of blue-shifted colour variants by rational design at atomic resolution, achieved through accurate hybrid molecular simulations, electrophysiology and X-ray crystallography. The molecular simulation models and the crystal structure reveal the precisely designed conformational changes of the chromophore induced by combinatory mutations that shrink its p-conjugated system which, together with electrostatic tuning, produce large blue shifts of the absorption spectra by maximally 100 nm, while maintaining photosensitive ion transport activities. The design principle we elaborate is applicable to other microbial opsins, and clarifies the underlying molecular mechanism of the blue-shifted action spectra of microbial opsins recently isolated from natural sources.
机译:具有结合的生色团的微生物视蛋白起光敏离子转运蛋白的作用,并已在光遗传学中用于神经元活性的光学控制。分子工程学已被用来创建颜色变体,以增强光遗传学工具的功能,但受到蛋白质-发色团相互作用的复杂性的限制。在这里,我们报告通过合理设计的原子分辨率,通过精确的混合分子模拟,电生理学和X射线晶体学研究,实现了蓝移色变体的发展。分子模拟模型和晶体结构揭示了由组合突变引起的发色团的精确设计构象变化,这些突变使它的p共轭体系收缩,再加上静电调谐,在最大吸收波长范围内最大吸收蓝移了100 nm,同时保持了光敏离子的运输活动。我们阐述的设计原理适用于其他微生物视蛋白,并阐明了最近从天然来源分离的微生物视蛋白的蓝移作用谱的潜在分子机理。

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