Electron transfer in DNA: covalent attachment of spectroscopically unique donor and acceptor complexes

被引:35
作者
Krider, ES [1 ]
Meade, TJ [1 ]
机构
[1] CALTECH, Beckman Inst, Pasadena, CA 91125 USA
来源
JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRY | 1998年 / 3卷 / 02期
关键词
electron-transfer reactions; DNA; distance dependence; ruthenium complexes;
D O I
10.1007/s007750050225
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The notion that DNA is capable of electron transfer (ET) has inspired several groups to investigate the nature of this intriguing process. While several factors modulate ET reaction rates, the distance dependence of ET in DNA is the focus of our current investigations. To this end we propose that several design criteria must be met to facilitate the collection of kinetic data corresponding to DNA-mediated ET reactions. These criteria include (1) covalent attachment of site-selective donor-acceptor pairs, (2) incorporation of donor-acceptor pairs that offer minimal structural perturbation of the DNA duplex, and (3) use of spectroscopically distinguishable donor and acceptor complexes that allow identification of kinetic intermediates.
引用
收藏
页码:222 / 225
页数:4
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