Electron hopping through the 15 Å triple tryptophan molecular wire in DNA photolyase occurs within 30 ps
The Journal of Physical Chemistry Part B: Condensed Matter, Materials, Surfaces, Interfaces & Biophysical , Volume 110 - Issue 32 p. 15654- 15658
Photoreduction of the semi-reduced flavin adenine dinucleotide cofactor FADḢ in DNA photolyase from Escherichia coli into FADH - involves three tryptophan (W) residues that form a closely spaced electron-transfer chain FADḢ-W382-W359-W306. To investigate this process, we have constructed a mutant photolyase in which W359 is replaced by phenylalanine (F). Monitoring its photoproducts by femtosecond spectroscopy, the excited-state FADḢ* was found to decay in ∼30 ps, similar as in wild type (WT) photolyase. In contrast to WT, however, in W359F mutant photolyase the ground-state FADḢ fully recovered virtually concomitantly with the decay of its excited state and, despite the presence of the primary electron donor W382, no measurable flavin reduction was observed at any time. Thus, W359F photolyase appears to behave like many other flavoproteins, where flavin excited states are quenched by very short-lived oxidation of aromatic residues. Our analysis indicates that both charge recombination of the primary charge separation state FADH-W382 ̇+ and (in WT) electron transfer from W359 to W382 ̇+ occur with time constants <4 ps, considerably faster than the initial W382→FADḢ* electron-transfer step. Our results provide a first experimental indication that electron transfer between aromatic residues can take place on the time scale of ∼10-12 s.
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|The Journal of Physical Chemistry Part B: Condensed Matter, Materials, Surfaces, Interfaces & Biophysical|
|Organisation||Erasmus MC: University Medical Center Rotterdam|
Lukacs, A, Eker, A.P.M, Byrdin, M, Villette, S, Pan, J, Brettel, K, & Vos, M.H. (2006). Electron hopping through the 15 Å triple tryptophan molecular wire in DNA photolyase occurs within 30 ps. The Journal of Physical Chemistry Part B: Condensed Matter, Materials, Surfaces, Interfaces & Biophysical, 110(32), 15654–15658. doi:10.1021/jp063686b