Issue 32, 2012

The road not taken: a theoretical view of an unexpected cryptochrome charge transfer path

Abstract

Motivated by recent progress in electron paramagnetic resonance spectroscopy, we describe hole transfer along a chain of tryptophan amino acids within the cryptochrome protein of Synechocystis sp.: surprisingly, despite a close sequential and structural similarity to E. coli DNA photolyase, the charge transfer paths and the final sites of charge localization are different for these two enzymes. We study this phenomenon using atomistic simulations and electronic structure computations as a theoretical basis, and we take a new look at the concepts of charge transfer and introduce a modification of Marcus' theory that incorporates dynamic polarization effects. Only this variant of theory describes the population of the correct branch on the subnanosecond time scale. Based on our numerical analysis, we further suggest that the Asp372–Arg374 salt bridge acts as a novel stepping stone in the charge transfer reaction.

Graphical abstract: The road not taken: a theoretical view of an unexpected cryptochrome charge transfer path

Article information

Article type
Paper
Submitted
13 3 2012
Accepted
27 6 2012
First published
27 6 2012

Phys. Chem. Chem. Phys., 2012,14, 11518-11524

The road not taken: a theoretical view of an unexpected cryptochrome charge transfer path

S. Krapf, S. Weber and T. Koslowski, Phys. Chem. Chem. Phys., 2012, 14, 11518 DOI: 10.1039/C2CP40793K

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