Structural and electronic property responses to the arsenic/phosphorus exchange in GC‐related DNA of the B‐form |
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| Authors: | Jiande Gu Jing Wang Yaoming Xie Jerzy Leszczynski Henry F Schaefer III |
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| Institution: | 1. Drug Design & Discovery Center, State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 201203, People's Republic of China;2. Department of Chemistry, Computational Center for Molecular Structure and Interactions, Jackson State University, Jackson, Mississippi 39217;3. Center for Computational Quantum Chemistry, University of Georgia, Athens, Georgia 30602‐2525 |
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| Abstract: | The suggestion that phosphorus/arsenic replacement in DNA can play a role in living things has generated great controversy (Wolfe‐Simon et al., Science 2011, 332, 1163). Examined here theoretically are substitution effects on Watson–Crick base pairing and base stacking patterns in realistic DNA subunits. Using duplex DNA models deoxyguanylyl‐3′,5′‐deoxycytidine (dGpdC]2) and deoxycytidyly‐3′,5′‐deoxyguanosine (dCpdG)]2), this research reveals that the geometric variations caused by the As/P exchange are small and are limited to the phosphate/arsenate groups. As/P replacement leads to alterations of ～0.15 Å in P/As? O bond lengths and less than 1.5° variations in O? P/As? O angles. The Watson–Crick base pairing and base stacking patterns are independent of the As/P replacement. The vertical electron detachment energies are also largely unaffected. However, the electron capture ability of the DNA units is improved by the As substitution. The arsenate is found to be the main electron acceptor in As‐DNA. The results are relevant to the possible existence of viable As‐DNAs, at least in the guanine and cytosine (GC)‐related B‐form DNA. © 2012 Wiley Periodicals, Inc. J Comput Chem, 2012 |
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| Keywords: | DNA As‐substitution DFT calculation electron affinity |
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