Biochemistry · 2001 · 53 citations · 30 references
Natural SciencesBiophysicsChemistryMolecular BiophysicsStructural BiologyStructural BiophysicsConformational AnalysisMacromolecular StructureMacromolecular Structure DeterminationPhotochemistryProtein ConformationProtein StructureChromophore PhotochemistryChromophore StructureDihedral AngleMacromolecular Structure CharacterizationMolecular ChromophoresNuclear Magnetic Resonance SpectroscopyProton AffinitySolid-state Nuclear Magnetic Resonance Spectroscopy
In recent years, structural information about bacteriorhodopsin has grown substantially with the publication of several crystal structures. However, precise measurements of the chromophore conformation in the various photocycle states are still lacking. This information is critical because twists about the chromophore backbone chain can influence the Schiff base nitrogen position, orientation, and proton affinity. Here, we focus on the C14-C15 bond, using solid-state nuclear magnetic resonance spectroscopy to measure the H-C14-C15-H dihedral angle. In the resting state (bR(568)), we obtain an angle of 164 +/- 4 degrees, indicating a 16 degrees distortion from a planar all-trans chromophore. The dihedral angle is found to decrease to 147 +/- 10 degrees in the early M intermediate (M(o)) and to 150 +/- 4 degrees in the late M intermediate (M(n)). These results demonstrate changes in the chromophore conformation undetected by recent X-ray diffraction studies.
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Structure of bacteriorhodopsin at 1.55 Å resolution
Hartmut Luecke, Brigitte Schobert, Hans-Thomas Richter et al. · Journal of Molecular Biology · 1999 · 1.5K citations
M. S. Lehmann, T. F. Koetzle, Walter C. Hamilton · Journal of the American Chemical Society · 1972 · 419 citations
A mechanism for the light-driven proton pump of Halobacterium halobium
Klaus Schulten, Paul Tavan · Nature · 1978 · 220 citations
Life Sciences, Biology, Microbiology +14