4YZI

Crystal structure of blue-shifted channelrhodopsin mutant (T198G/G202A)

4YZI の概要

• エントリーDOI: 10.2210/pdb4yzi/pdb
• 分子名称: Sensory opsin A,Archaeal-type opsin 2, RETINAL, OLEIC ACID, ... (5 entities in total)
• 機能のキーワード: membrane protein, channelrhodopsin, microbial rhodopsin
• 由来する生物種: Chlamydomonas reinhardtii
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 36318.20

構造登録者

Kato, H.E.,Kamiya, M.,Ishitani, R.,Hayashi, S.,Nureki, O. (登録日: 2015-03-25, 公開日: 2015-05-27, 最終更新日: 2020-02-19)

主引用文献

Kato, H.E.,Kamiya, M.,Sugo, S.,Ito, J.,Taniguchi, R.,Orito, A.,Hirata, K.,Inutsuka, A.,Yamanaka, A.,Maturana, A.D.,Ishitani, R.,Sudo, Y.,Hayashi, S.,Nureki, O.
Atomistic design of microbial opsin-based blue-shifted optogenetics tools.
Nat Commun, 6:7177-7177, 2015

PubMed 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.

PubMed: 25975962
DOI: 10.1038/ncomms8177

実験手法

X-RAY DIFFRACTION (2.5 Å)