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4YZI

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

Summary for 4YZI
Entry DOI10.2210/pdb4yzi/pdb
DescriptorSensory opsin A,Archaeal-type opsin 2, RETINAL, OLEIC ACID, ... (5 entities in total)
Functional Keywordsmembrane protein, channelrhodopsin, microbial rhodopsin
Biological sourceChlamydomonas reinhardtii
Total number of polymer chains1
Total formula weight36318.20
Authors
Kato, H.E.,Kamiya, M.,Ishitani, R.,Hayashi, S.,Nureki, O. (deposition date: 2015-03-25, release date: 2015-05-27, Last modification date: 2024-11-20)
Primary citationKato, 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
Cited by
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
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.5 Å)
Structure validation

231029

數據於2025-02-05公開中

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