Remarkable hydrogen bonding in the radical anions of guanine-cytosine and adenine-thymine

被引:2
|
作者
Peng, Bin [1 ]
McNew, Shane R. [2 ]
Li, Qian-Shu [1 ]
Xie, Yaoming [2 ]
Schaefer, Henry F., III [2 ]
机构
[1] S China Normal Univ, Ctr Computat Quantum Chem, Key Lab Theoret Chem Environm, Minist Educ, Guangzhou 510631, Guangdong, Peoples R China
[2] Univ Georgia, Ctr Computat Chem, Athens, GA 30602 USA
基金
美国国家科学基金会;
关键词
BASE-PAIR;
D O I
10.1016/j.cplett.2011.12.003
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Capture of an electron by either DNA base pair results in a major structural reorganization. One of the peripheral hydrogen bonds is significantly lengthened (0.22 angstrom in GC(-)) and the other significantly shortened (0.30 angstrom in AT(-)). These striking structural shifts are predicted by the MP2 method. We argue that the correct electronic description of the two anions is G[C-] and A[T-], displaying hydrogen bonding between the neutral purine base and the pyrimidine radical anion. This hypothesis is tested via higher level studies of thymine and its radical anion. The experimental conformation or denial of these predictions will provide a major step in our understanding of the structures of biomolecules. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:120 / 123
页数:4
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