The structure and dynamics of the retinal chromophore of rhodopsin are investigated systematically in different environments (vacuum, methanol solution, and protein binding pocket) and with different computational approaches (classical, quantum, and hybrid quantum mechanics/molecular mechanics (QM/MM) descriptions).Finite temperature effects are taken into account by molecular dynamics simulations.The different components that determine the structure and dynamics of the chromophore in the protein are dissected, both in the dark state and in the early photointermediates.In vacuum and in solution the chromophore displays a very high flexibility, which is significantly reduced by the protein environment.In the 11-cis chromophore, the bond-length alternation, which is correlated with the dipole moment, is found to be similar in solution and in the protein, while it differs greatly with respect to minimum-energy vacuum structures.In the model of the earliest protein photointermediate, the highly twisted chromophore shows a very reduced bondlength alternation.

Solvent and protein effects on the structure and dynamics of the rhodopsin chromophore

GUIDONI, Leonardo;
2005-01-01

Abstract

The structure and dynamics of the retinal chromophore of rhodopsin are investigated systematically in different environments (vacuum, methanol solution, and protein binding pocket) and with different computational approaches (classical, quantum, and hybrid quantum mechanics/molecular mechanics (QM/MM) descriptions).Finite temperature effects are taken into account by molecular dynamics simulations.The different components that determine the structure and dynamics of the chromophore in the protein are dissected, both in the dark state and in the early photointermediates.In vacuum and in solution the chromophore displays a very high flexibility, which is significantly reduced by the protein environment.In the 11-cis chromophore, the bond-length alternation, which is correlated with the dipole moment, is found to be similar in solution and in the protein, while it differs greatly with respect to minimum-energy vacuum structures.In the model of the earliest protein photointermediate, the highly twisted chromophore shows a very reduced bondlength alternation.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11697/21221
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