DFT study of polymorphism of the DNA double helix at the level of dinucleoside monophosphates |
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| Authors: | Valeri I. Poltev Victor M. Anisimov Victor I. Danilov Tanja van Mourik Alexandra Deriabina Eduardo González Maria Padua Dolores Garcia Francisco Rivas Nina Polteva |
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| Affiliation: | 1. Autonomous University of Puebla, Puebla 72570, Mexico;2. Institute of Theoretical and Experimental Biophysics, RAS, Pushchino 142290, Russia;3. School of Health Information Sciences, University of Texas, 7000 Fannin St, Houston, TX 77030;4. Institute of Molecular Biology and Genetics, Kiev 03143, Ukraine;5. School of Chemistry, University of St. Andrews, North Haugh Fife, KY16 9ST, Scotland, United Kingdom |
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| Abstract: | We apply DFT calculations to deoxydinucleoside monophosphates (dDMPs) which represent minimal fragments of the DNA chain to study the molecular basis of stability of the DNA duplex, the origin of its polymorphism and conformational heterogeneity. In this work, we continue our previous studies of dDMPs where we detected internal energy minima corresponding to the “classical” B conformation (BI‐form), which is the dominant form in the crystals of oligonucleotide duplexes. We obtained BI local energy minima for all existing base sequences of dDMPs. In the present study, we extend our analysis to other families of DNA conformations, successfully identifying A, BI, and BII energy minima for all dDMP sequences. These conformations demonstrate distinct differences in sugar ring puckering, but similar sequence‐dependent base arrangements. Internal energies of BI and BII conformers are close to each other for nearly all the base sequences. The dGpdG, dTpdG, and dCpdA dDMPs slightly favor the BII conformation, which agrees with these sequences being more frequently experimentally encountered in the BII form. We have found BII‐like structures of dDMPs for the base sequences both existing in crystals in BII conformation and those not yet encountered in crystals till now. On the other hand, we failed to obtain dDMP energy minima corresponding to the Z family of DNA conformations, thus giving us the ground to conclude that these conformations are stabilized in both crystals and solutions by external factors, presumably by interactions with various components of the media. Overall the accumulated computational data demonstrate that the A, BI, and BII families of DNA conformations originate from the corresponding local energy minimum conformations of dDMPs, thus determining structural stability of a single DNA strand during the processes of unwinding and rewinding of DNA. © 2010 Wiley Periodicals, Inc. Int J Quantum Chem 110:2548–2559, 2010 |
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| Keywords: | DNA dDMP nucleoside nucleoside conformation DFT calculations |
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