Sequence Dependent Long Range Hole Transport in DNA

Eric Meggers(University of Basel), M.E. Michel‐Beyerle(University of Basel), Bernd Giese(University of Basel)
Journal of the American Chemical Society
November 24, 1998
Cited by 669

Abstract

A guanine radical cation (G+•) was site-selectively generated in double stranded DNA and the charge transfer in different oligonucleotide sequences was investigated. The method is based on the competition between a charge transfer from G+• through the DNA and its trapping reaction with H2O. We analyzed the hole transfer from this G+• to a GGG unit through one, two, three, and four AT base pairs and found that the rate decreases by about 1 order of magnitude with each intervening AT base pair. This strong distance dependence led to a β-value of 0.7 ± 0.1 Å-1. Within the time scale of this assay the charge transfer nearly vanished when the G+• was separated by four AT base pairs from the GGG unit. However, if the second or the third of the four intervening AT base pairs was exchanged by a GC base pair, the rate of the hole transfer from the G+• to the GGG unit increased by 2 orders of magnitude. In addition, a long-range charge transfer over 15 base pairs could be observed in a mixed strand that contained AT as well as GC base pairs. Because G+• can oxidize G but not A bases, the long-range charge transport can be explained by a hopping of the positive charge between the intervening G bases. Thus, the overall charge transport in a mixed strand is a multistep hopping process between G bases where the individual steps contribute to the overall rate. The distance dependence is no longer described by the β value of the superexchange mechanism.


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