DFT Study of Polymorphism of the DNA Double Helix at the Level of Dinucleoside Monophosphates

被引:15
作者
Poltev, Valeri I. [1 ,2 ]
Anisimov, Victor M. [3 ]
Danilov, Victor I. [4 ]
Van Mourik, Tanja [5 ]
Deriabina, Alexandra [1 ]
Gonzalez, Eduardo [1 ]
Padua, Maria [1 ]
Garcia, Dolores [1 ]
Rivas, Francisco [1 ]
Polteva, Nina [2 ]
机构
[1] Autonomous Univ Puebla, Puebla 72570, Mexico
[2] RAS, Inst Theoret & Expt Biophys, Pushchino 142290, Russia
[3] Univ Texas Houston, Sch Hlth Informat Sci, Houston, TX 77030 USA
[4] Inst Mol Biol & Genet, UA-03143 Kiev, Ukraine
[5] Univ St Andrews, Sch Chem, St Andrews KY16 9ST, Fife, Scotland
关键词
DNA; dDMP; nucleoside; nucleoside conformation; DFT calculations; DENSITY-FUNCTIONAL THEORY; VAN-DER-WAALS; INTERACTION ENERGIES; COMPLEXES; ACCURATE; CONFORMATIONS; DYNAMICS; SUGAR; SET;
D O I
10.1002/qua.22748
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
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. (C) 2010 Wiley Periodicals, Inc. Int J Quantum Chem 110: 2548-2559, 2010
引用
收藏
页码:2548 / 2559
页数:12
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