The role of intersection topography in bond selectivity of cis-trans photoisomerization

February 19, 2002
99 (4) 1769-1773

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.

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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.

Supplementary Material

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Information & Authors

Information

Published in

The cover image for PNAS Vol.99; No.4
Proceedings of the National Academy of Sciences
Vol. 99 | No. 4
February 19, 2002
PubMed: 11854479

Classifications

Submission history

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.

Authors

Affiliations

M. Ben-Nun
Departments of Chemistry and Physics, University of Illinois, 600 S. Mathews, Urbana, IL 61801; and The Beckman Institute for Advanced Science and Technology, 405 N. Mathews, Urbana, IL 61801
F. Molnar
Departments of Chemistry and Physics, University of Illinois, 600 S. Mathews, Urbana, IL 61801; and The Beckman Institute for Advanced Science and Technology, 405 N. Mathews, Urbana, IL 61801
K. Schulten§
Departments of Chemistry and Physics, University of Illinois, 600 S. Mathews, Urbana, IL 61801; and The Beckman Institute for Advanced Science and Technology, 405 N. Mathews, Urbana, IL 61801
Todd J. Martínez§
Departments of Chemistry and Physics, University of Illinois, 600 S. Mathews, Urbana, IL 61801; and The Beckman Institute for Advanced Science and Technology, 405 N. Mathews, Urbana, IL 61801

Notes

§
To whom reprint requests should be addressed. E-mail: [email protected] (T.J.M.) or [email protected] (K.S.).
Communicated by Peter G. Wolynes, University of California at San Diego, La Jolla, CA

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    The role of intersection topography in bond selectivity of cis-trans photoisomerization
    Proceedings of the National Academy of Sciences
    • Vol. 99
    • No. 4
    • pp. 1749-2461

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