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6GA6

Bacteriorhodopsin, 10 ps state, real-space refined against 10% extrapolated map

Summary for 6GA6
Entry DOI10.2210/pdb6ga6/pdb
DescriptorBacteriorhodopsin, nonane, TETRADECANE, ... (12 entities in total)
Functional Keywordsmembrane protein, proton pump, time-resolved crystallography, free-electron laser
Biological sourceHalobacterium salinarum (strain ATCC 700922 / JCM 11081 / NRC-1) (Halobacterium halobium)
Total number of polymer chains1
Total formula weight30794.61
Authors
Primary citationNass 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: 31320619
DOI: 10.1038/s41467-019-10758-0
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.8 Å)
Structure validation

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