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Photoselected Electron Transfer Pathways in DNA Photolyase

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Specialty Science
Date 2007 Jan 9
PMID 17209014
Citations 26
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Abstract

Cyclobutane dimer photolyases are proteins that bind to UV-damaged DNA containing cyclobutane pyrimidine dimer lesions. They repair these lesions by photo-induced electron transfer. The electron donor cofactor of a photolyase is a two-electron-reduced flavin adenine dinucleotide (FADH(-)). When FADH(-) is photo-excited, it transfers an electron from an excited pi --> pi* singlet state to the pyrimidine dimer lesion of DNA. We compute the lowest excited singlet states of FADH(-) using ab initio (time-dependent density functional theory and time-dependent Hartree-Fock), and semiempirical (INDO/S configuration interaction) methods. The calculations show that the two lowest pi --> pi* singlet states of FADH(-) are localized on the side of the flavin ring that is proximal to the dimer lesion of DNA. For the lowest-energy donor excited state of FADH(-), we compute the conformationally averaged electronic coupling to acceptor states of the thymine dimer. The coupling calculations are performed at the INDO/S level, on donor-acceptor cofactor conformations obtained from molecular dynamics simulations of the solvated protein with a thymine dimer docked in its active site. These calculations demonstrate that the localization of the (1)FADH(-)* donor state on the flavin ring enhances the electronic coupling between the flavin and the dimer by permitting shorter electron-transfer pathways to the dimer that have single through-space jumps. Therefore, in photolyase, the photo-excitation itself enhances the electron transfer rate by moving the electron towards the dimer.

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References
1.
Case D, Cheatham 3rd T, Darden T, Gohlke H, Luo R, Merz Jr K . The Amber biomolecular simulation programs. J Comput Chem. 2005; 26(16):1668-88. PMC: 1989667. DOI: 10.1002/jcc.20290. View

2.
Park H, Kim S, Sancar A, Deisenhofer J . Crystal structure of DNA photolyase from Escherichia coli. Science. 1995; 268(5219):1866-72. DOI: 10.1126/science.7604260. View

3.
Christine K, MacFarlane 4th A, Yang K, Stanley R . Cyclobutylpyrimidine dimer base flipping by DNA photolyase. J Biol Chem. 2002; 277(41):38339-44. DOI: 10.1074/jbc.M206531200. View

4.
Ponder J, Case D . Force fields for protein simulations. Adv Protein Chem. 2003; 66:27-85. DOI: 10.1016/s0065-3233(03)66002-x. View

5.
Gauden M, Yeremenko S, Laan W, van Stokkum I, Ihalainen J, van Grondelle R . Photocycle of the flavin-binding photoreceptor AppA, a bacterial transcriptional antirepressor of photosynthesis genes. Biochemistry. 2005; 44(10):3653-62. DOI: 10.1021/bi047359a. View