Flavin Charge Transfer Transitions Assist DNA Photolyase Electron Transfer.


Journal Article

This contribution describes molecular dynamics, semi-empirical and ab-initio studies of the primary photo-induced electron transfer reaction in DNA photolyase. DNA photolyases are FADH(-)-containing proteins that repair UV-damaged DNA by photo-induced electron transfer. A DNA photolyase recognizes and binds to cyclobutatne pyrimidine dimer lesions of DNA. The protein repairs a bound lesion by transferring an electron to the lesion from FADH(-), upon photo-excitation of FADH(-) with 350-450 nm light. We compute the lowest singlet excited states of FADH(-) in DNA photolyase using INDO/S configuration interaction, time-dependent density-functional, and time-dependent Hartree-Fock methods. The calculations identify the lowest singlet excited state of FADH(-) that is populated after photo-excitation and that acts as the electron donor. For this donor state we compute conformationally-averaged tunneling matrix elements to empty electron- acceptor states of a thymine dimer bound to photolyase. The conformational averaging involves different FADH(-) - thymine dimer confromations obtained from molecular dynamics simulations of the solvated protein with a thymine dimer docked in its active site. The tunneling matrix element computations use INDO/S-level Green's function, energy splitting, and Generalized Mulliken-Hush methods. These calculations indicate that photo-excitation of FADH(-) causes a π → π(*) charge-transfer transition that shifts electron density to the side of the flavin isoalloxazine ring that is adjacent to the docked thymine dimer. This shift in electron density enhances the FADH(-) - to - dimer electronic coupling, thus inducing rapid electron transfer.

Full Text

Duke Authors

Cited Authors

  • Skourtis, SS; Prytkova, T; Beratan, DN

Published Date

  • January 1, 2007

Published In

Volume / Issue

  • 963 /

Start / End Page

  • 674 - 677

PubMed ID

  • 23226907

Pubmed Central ID

  • 23226907

Electronic International Standard Serial Number (EISSN)

  • 1551-7616

International Standard Serial Number (ISSN)

  • 0094-243X

Digital Object Identifier (DOI)

  • 10.1063/1.2836174


  • eng