The role of intersection topography in bond selectivity of cis-trans photoisomerization
Abstract
Ab initio methods are used to characterize the ground and first excited state of the chromophore in the rhodopsin family of proteins: retinal protonated Schiff base. Retinal protonated Schiff base has five double bonds capable of undergoing isomerization. Upon absorption of light, the chromophore isomerizes and the character of the photoproducts (e.g., 13-cis and 11-cis) depends on the environment, protein vs. solution. Our ab initio calculations show that, in the absence of any specific interactions with the environment (e.g., discrete ordered charges in a protein), energetic considerations cannot explain the observed bond selectivity. We instead attribute the origin of bond selectivity to the shape (topography) of the potential energy surfaces in the vicinity of points of true degeneracy (conical intersections) between the ground and first excited electronic states. This provides a molecular example where a competition between two distinct but nearly isoenergetic photochemical reaction pathways is resolved by a topographical difference between two conical intersections.
Acknowledgments
This work was supported by the National Science Foundation (CHE-97-33403 and DMR-99-76550) and National Institutes of Health (PHS-5-P41-RR05969). Computing support through National Resources Allocation Committee MCA93S028 is gratefully acknowledged. T.J.M. thanks the Sloan Foundation, Beckman Foundation, Packard Foundation, National Science Foundation, and Dreyfus Foundation for support through a Sloan Fellowship, Beckman Young Investigator Award, Packard Fellowship, CAREER Award, and a Dreyfus Teacher-Scholar Fellowship, respectively.
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Copyright © 2002, The National Academy of Sciences.
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Received: August 7, 2001
Accepted: December 10, 2001
Published online: February 19, 2002
Published in issue: February 19, 2002
Acknowledgments
This work was supported by the National Science Foundation (CHE-97-33403 and DMR-99-76550) and National Institutes of Health (PHS-5-P41-RR05969). Computing support through National Resources Allocation Committee MCA93S028 is gratefully acknowledged. T.J.M. thanks the Sloan Foundation, Beckman Foundation, Packard Foundation, National Science Foundation, and Dreyfus Foundation for support through a Sloan Fellowship, Beckman Young Investigator Award, Packard Fellowship, CAREER Award, and a Dreyfus Teacher-Scholar Fellowship, respectively.
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The role of intersection topography in bond selectivity of cis-trans photoisomerization, Proc. Natl. Acad. Sci. U.S.A.
99 (4) 1769-1773,
https://doi.org/10.1073/pnas.032658099
(2002).
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