Electronic Structure of DNA - Unique Properties of 8-Oxoguanosine

被引:22
作者
Markus, Tal Z. [1 ]
Daube, Shirley S.
Naaman, Ron [1 ]
Fleming, Aaron M. [2 ]
Muller, James G. [2 ]
Burrows, Cynthia J. [2 ]
机构
[1] Weizmann Inst Sci, Dept Chem Phys, IL-76100 Rehovot, Israel
[2] Univ Utah, Dept Chem, Salt Lake City, UT 84112 USA
基金
美国国家科学基金会; 以色列科学基金会;
关键词
SELF-ASSEMBLED MONOLAYERS; LOW-ENERGY ELECTRONS; ORGANIC/METAL INTERFACES; GAS-PHASE; PHOTOEMISSION; DYNAMICS; FEMTOSECOND; EXCISION; REPAIR; BASES;
D O I
10.1021/ja804177j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
8-Oxo-7,8-dihydroguanosine (8-oxoG) is among the most common forms of oxidative DNA damage found in human cells. The question of damage recognition by the repair machinery is a long standing one, and it is intriguing to suggest that the mechanism of efficiently locating damage within the entire genome might be related to modulations in the electronic properties of lesions compared to regular bases. Using laser-based methods combined with organizing various oligomers self-assembled monolayers on gold substrates, we show that indeed 8-oxoG has special electronic properties. By using oligomers containing 8-oxoG and guanine bases which were inserted in an all thymine sequences, we were able to determine the energy of the HOMO and LUMO states and the relative density of electronic states below the vacuum level. Specifically, it was found that when 8-oxoG is placed in the oligomer, the HOMO state is at higher energy than in the other oligomers studied. In contrast, the weakly mutagenic 8-oxo-7,8-dihydroadenosine (8-oxoA) has little or no effect on the electronic properties of DNA.
引用
收藏
页码:89 / 95
页数:7
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