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用强配对的第五碱基取代胸腺嘧啶:量子力学与分子动力学的联合研究

Replacing thymine with a strongly pairing fifth Base: A combined quantum mechanics and molecular dynamics study.

作者信息

Chawla Mohit, Gorle Suresh, Shaikh Abdul Rajjak, Oliva Romina, Cavallo Luigi

机构信息

King Abdullah University of Science and Technology (KAUST), Physical Sciences and Engineering Division, Kaust Catalysis Center, Thuwal 23955-6900, Saudi Arabia.

Department of Biochemistry and Molecular Biology, University of Texas Medical Branch, Galveston, TX 77555, USA.

出版信息

Comput Struct Biotechnol J. 2021 Feb 23;19:1312-1324. doi: 10.1016/j.csbj.2021.02.006. eCollection 2021.

Abstract

The non-natural ethynylmethylpyridone C-nucleoside (W), a thymidine (T) analogue that can be incorporated in oligonucleotides by automated synthesis, has recently been reported to form a high fidelity base pair with adenosine (A) and to be well accommodated in B-DNA duplexes. The enhanced binding affinity for A of W, as compared to T, makes it an ideal modification for biotechnological applications, such as efficient probe hybridization for the parallel detection of multiple DNA strands. In order to complement the experimental study and rationalize the impact of the non-natural W nucleoside on the structure, stability and dynamics of DNA structures, we performed quantum mechanics (QM) calculations along with molecular dynamics (MD) simulations. Consistently with the experimental study, our QM calculations show that the A:W base pair has an increased stability as compared to the natural A:T pair, due to an additional CH-π interaction. Furthermore, we show that mispairing between W and guanine (G) causes a distortion in the planarity of the base pair, thus explaining the destabilization of DNA duplexes featuring a G:W pair. MD simulations show that incorporation of single or multiple consecutive A:W pairs in DNA duplexes causes minor changes to the intra- and inter-base geometrical parameters, while a moderate widening/shrinking of the major/minor groove of the duplexes is observed. QM calculations applied to selected stacks from the MD simulations also show an increased stacking energy for W, over T, with the neighboring bases.

摘要

非天然乙炔基甲基吡啶酮C-核苷(W)是一种胸腺嘧啶核苷(T)类似物,可通过自动合成掺入寡核苷酸中。最近有报道称,它能与腺苷(A)形成高保真碱基对,并能很好地容纳在B-DNA双链体中。与T相比,W对A的结合亲和力增强,这使其成为生物技术应用的理想修饰,例如用于平行检测多条DNA链的高效探针杂交。为了补充实验研究并阐明非天然W核苷对DNA结构的结构、稳定性和动力学的影响,我们进行了量子力学(QM)计算以及分子动力学(MD)模拟。与实验研究一致,我们的QM计算表明,与天然A:T碱基对相比,A:W碱基对的稳定性有所提高,这是由于额外的CH-π相互作用。此外,我们表明W与鸟嘌呤(G)之间的错配会导致碱基对平面性的扭曲,从而解释了具有G:W对的DNA双链体的不稳定。MD模拟表明,在DNA双链体中掺入单个或多个连续的A:W对会导致碱基内和碱基间几何参数的微小变化,同时观察到双链体的大沟/小沟有适度的加宽/变窄。应用于MD模拟中选定堆叠的QM计算还表明,与T相比,W与相邻碱基的堆叠能量增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/882e/7940798/830ff8fce426/ga1.jpg

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