新型光驱动钠泵的研究及新功能分子的制备

Keiichi Inoue
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引用次数: 0

摘要

微生物紫红质是微生物的光接受膜蛋白。最普遍存在的微生物紫红质是光驱动离子泵,它主动运输H+或clon膜化学势。2013年,我们报道了一类新的离子泵视紫红质——钠泵视紫红质(sodium pump rhodopsin, KR2),它利用光能向外输送Na+离子。用光谱和晶体学方法研究了KR2对Na+的输运机制。结果表明,H+在光异构化的视网膜席夫碱及其反离子Asp116之间的转移是Na+转运功能的关键过程。在H+转移之后,质子化的Asp116将H+从离子运输途径中隔离出来,然后立即从细胞质侧吸收Na+。Na+结合到Asn112和Asp251组成的位点上,同时H+回到视网膜的希夫碱基上。然后,再生的视网膜希夫碱的正电荷阻止Na+回流到细胞质侧。最后,Na+被释放到细胞外。此外,在对KR2结构认识的基础上,我们成功地开发了新的人工K+和Cs+泵送KR2突变体,分别是KR2K+和kr2c +。野生型KR2和这些突变体有望为光遗传学的应用提供新的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Study on a Novel Light-driven Sodium Pump and Creation of New Functional Molecules
Microbial rhodopsin is a photo-receptive membrane protein of micro-organisms. The most ubiquitous microbial rhodopsins are light-driven ion pumps which actively transport H+ or Clagainst membrane chemical potential. In 2013, we reported a new class of ion pump rhodopsin, sodium pump rhodopsin (KR2) which outwardly transports Na+ ion by the use of light energy. The mechanism of Na+ transport by KR2 was investigated in spectroscopic and crystallographic studies. The results showed that the H+ transfer between photoisomerized retinal Schiff base and its counter ion, Asp116, is a critical process for the Na+-transport function. After this H+ transfer, the protonated Asp116 sequesters the H+ from the ion-transport pathway, and then immediately Na+ is taken up from the cytoplasmic side. The Na+ binds to the site composed of Asn112 and Asp251, and simultaneously H+ goes back to the retinal Schiff base. Then, positive charge of the reprotonated retinal Schiff-base prevents the back flow of Na+ to the cytoplasmic side. Finally, the Na+ is released to the extracellular side. Furthermore, on the basis of structural insights about KR2, we have succeeded to develop new artificial K+ and Cs+ pumping KR2 mutants, KR2K+ and KR2Cs+, respectively. Wildtype KR2 and these mutants are expected to provide new ways of the application to optogenetics.
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