6GA5
Bacteriorhodopsin, 3 ps state, REAL-SPACE REFINEMED AGAINST 10% EXTRAPOLATED MAP
Summary for 6GA5
Entry DOI | 10.2210/pdb6ga5/pdb |
Descriptor | Bacteriorhodopsin, nonane, TETRADECANE, ... (12 entities in total) |
Functional Keywords | membrane protein, proton pump, time-resolved crystallography, free-electron laser |
Biological source | Halobacterium salinarum (strain ATCC 700922 / JCM 11081 / NRC-1) (Halobacterium halobium) |
Total number of polymer chains | 1 |
Total formula weight | 30794.61 |
Authors | Nass Kovacs, G.,Colletier, J.-P.,Gruenbein, M.L.,Stensitzki, T.,Batyuk, A.,Carbajo, S.,Doak, R.B.,Ehrenberg, D.,Foucar, L.,Gasper, R.,Gorel, A.,Hilpert, M.,Kloos, M.,Koglin, J.,Reinstein, J.,Roome, C.M.,Schlesinger, R.,Seaberg, M.,Shoeman, R.L.,Stricker, M.,Boutet, S.,Haacke, S.,Heberle, J.,Domratcheva, T.,Schlichting, I. (deposition date: 2018-04-11, release date: 2019-04-24, Last modification date: 2019-07-31) |
Primary citation | Nass Kovacs, G.,Colletier, J.P.,Grunbein, M.L.,Yang, Y.,Stensitzki, T.,Batyuk, A.,Carbajo, S.,Doak, R.B.,Ehrenberg, D.,Foucar, L.,Gasper, R.,Gorel, A.,Hilpert, M.,Kloos, M.,Koglin, J.E.,Reinstein, J.,Roome, C.M.,Schlesinger, R.,Seaberg, M.,Shoeman, R.L.,Stricker, M.,Boutet, S.,Haacke, S.,Heberle, J.,Heyne, K.,Domratcheva, T.,Barends, T.R.M.,Schlichting, I. Three-dimensional view of ultrafast dynamics in photoexcited bacteriorhodopsin. Nat Commun, 10:3177-3177, 2019 Cited by PubMed Abstract: Bacteriorhodopsin (bR) is a light-driven proton pump. The primary photochemical event upon light absorption is isomerization of the retinal chromophore. Here we used time-resolved crystallography at an X-ray free-electron laser to follow the structural changes in multiphoton-excited bR from 250 femtoseconds to 10 picoseconds. Quantum chemistry and ultrafast spectroscopy were used to identify a sequential two-photon absorption process, leading to excitation of a tryptophan residue flanking the retinal chromophore, as a first manifestation of multiphoton effects. We resolve distinct stages in the structural dynamics of the all-trans retinal in photoexcited bR to a highly twisted 13-cis conformation. Other active site sub-picosecond rearrangements include correlated vibrational motions of the electronically excited retinal chromophore, the surrounding amino acids and water molecules as well as their hydrogen bonding network. These results show that this extended photo-active network forms an electronically and vibrationally coupled system in bR, and most likely in all retinal proteins. PubMed: 31320619DOI: 10.1038/s41467-019-10758-0 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.9 Å) |
Structure validation
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