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QM/MM calculations of retinal protein excited states: Investigating the mechanisms of color tuning

Fachliche Zuordnung Optik, Quantenoptik und Physik der Atome, Moleküle und Plasmen
Förderung Förderung von 2005 bis 2011
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 5469831
 
Although the proteins bR and Rh contain the same chromophore, a protonated retinal Schiff base, the absorption maxima are shifted differently in the different protein matrices compared to the spectrum of the isolated retinal (¿copsin shift ). This is due to the interaction of the chromophore with various amino acids in the different protein pockets. Further, the photoisomerization in the protein differs significantly from that in solution, concerning its velocity, the reaction coordinate and quantum yield.In this project we investigate the specific interactions of the proteins with the chromophore in its electronically excited state. These investigations are now feasible, since only recently crystal structures of various intermediates with sufficient resolution became available, and appropriate theoretical methods have been developed. The goal of this proposal is to investigate the influence of steric and electrostatic interactions of amino acid residues from the protein pocket an the optical properties of the chromophore. Further, the spectral changes due to rearrangement of the protein during the photo cycle and the changes due to mutations of the amino acid sequence will be investigated.
DFG-Verfahren Forschungsgruppen
 
 

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