ChemistryOpen | |
B‐DNA Structure and Stability as Function of Nucleic Acid Composition: Dispersion‐Corrected DFT Study of Dinucleoside Monophosphate Single and Double Strands | |
Dr. Giampaolo Barone1  Dr. Célia Fonseca Guerra2  | |
[1] 关键词: density functional calculations; DNA structures; hydrogen bonds; stacking interactions; Watson–Crick base pairs; | |
DOI : 10.1002/open.201300019 | |
来源: Wiley | |
【 摘 要 】
We have computationally investigated the structure and stability of all 16 combinations of two out of the four natural DNA bases A, T, G and C in a di-2′-deoxyribonucleoside-monophosphate model DNA strand as well as in 10 double-strand model complexes thereof, using dispersion-corrected density functional theory (DFT-D). Optimized geometries with B-DNA conformation were obtained through the inclusion of implicit water solvent and, in the DNA models, of sodium counterions, to neutralize the negative charge of the phosphate groups. The results obtained allowed us to compare the relative stability of isomeric single and double strands. Moreover, the energy of the Watson–Crick pairing of complementary single strands to form double-helical structures was calculated. The latter furnished the following increasing stability trend of the double-helix formation energy: d(TpA)2 Abstract
【 授权许可】
Unknown
© 2013 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
【 预 览 】
Files | Size | Format | View |
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RO202107150004423ZK.pdf | 1703KB | download |