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基于微生物视蛋白的蓝移光遗传学工具的原子设计

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

作者信息

Kato Hideaki E, Kamiya Motoshi, Sugo Seiya, Ito Jumpei, Taniguchi Reiya, Orito Ayaka, Hirata Kunio, Inutsuka Ayumu, Yamanaka Akihiro, Maturana Andrés D, Ishitani Ryuichiro, Sudo Yuki, Hayashi Shigehiko, Nureki Osamu

机构信息

Department of Biological Sciences, Graduate School of Science, The University of Tokyo, 2-11-16 Yayoi, Bunkyo-ku, Tokyo 113-0032, Japan.

Department of Chemistry, Graduate School of Science, Kyoto University, Kyoto 606-8502, Japan.

出版信息

Nat Commun. 2015 May 15;6:7177. doi: 10.1038/ncomms8177.

Abstract

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 π-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.

摘要

结合有发色团的微生物视蛋白可作为光敏离子转运体,并已被应用于光遗传学中以光学方式控制神经元活动。分子工程已被用于创造颜色变体以增强光遗传学工具的功能,但受到蛋白质 - 发色团相互作用复杂性的限制。在此,我们报告通过精确的混合分子模拟、电生理学和X射线晶体学,在原子分辨率下通过合理设计开发出蓝移颜色变体。分子模拟模型和晶体结构揭示了由组合突变诱导的发色团精确设计的构象变化,这些突变缩小了其π共轭体系,与静电调节一起,使吸收光谱产生最大100nm的大蓝移,同时保持光敏离子转运活性。我们阐述的设计原则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蓝移作用光谱的潜在分子机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bfe/4479019/57c2742d5738/ncomms8177-f1.jpg

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