4YZI
Crystal structure of blue-shifted channelrhodopsin mutant (T198G/G202A)
Summary for 4YZI
Entry DOI | 10.2210/pdb4yzi/pdb |
Descriptor | Sensory opsin A,Archaeal-type opsin 2, RETINAL, OLEIC ACID, ... (5 entities in total) |
Functional Keywords | membrane protein, channelrhodopsin, microbial rhodopsin |
Biological source | Chlamydomonas reinhardtii |
Total number of polymer chains | 1 |
Total formula weight | 36318.20 |
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 citation | 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 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: 25975962DOI: 10.1038/ncomms8177 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.5 Å) |
Structure validation
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