†U.S. Army Research Laboratory, Aberdeen Proving Ground, MD 21005, United States.
‡Department of Chemical and Biological Engineering, University of Colorado, Boulder, Colorado 80309, United States.
Biomacromolecules. 2015 Jun 8;16(6):1862-9. doi: 10.1021/acs.biomac.5b00469. Epub 2015 May 21.
DNA hybridization is the foundation for numerous technologies like DNA origami and DNA sensing/microarrays. Using molecular simulations, enhanced-sampling methods, and free-energy calculations, we show the effects of hydrophilic and hydrophobic surfaces on DNA hybridization. Hydrophilic surfaces compete with terminal bases' H-bonds but stabilize central base stacking. Hydrophobic surfaces strengthen terminal H-bonds but destabilize central base stacking. Regardless of surface chemistry, for terminal bases, melting proceeds through breaking H-bonds, followed by unstacking from the neighboring base. For central bases in bulk or near hydrophobic surfaces, melting proceeds by disruption of H-bonds, followed by unstacking, whereas on hydrophilic surfaces, unstacking from one neighboring base precedes complete disruption of the H-bonds, followed by unstacking from the second neighboring base. Kinetic barriers to melting and hybridization show that the central bases melt rapidly near hydrophobic surfaces, which can accelerate conformational searching and thereby accelerate folding into the desired conformation.
DNA 杂交是许多技术的基础,如 DNA 折纸术和 DNA 感测/微阵列。我们使用分子模拟、增强采样方法和自由能计算,研究了亲水性和疏水性表面对 DNA 杂交的影响。亲水性表面与末端碱基的氢键竞争,但稳定了中心碱基堆积。疏水性表面增强了末端氢键,但破坏了中心碱基堆积。无论表面化学性质如何,对于末端碱基,熔融过程是通过打破氢键,然后从相邻碱基上解叠。对于体相或靠近疏水性表面的中心碱基,熔融过程是通过破坏氢键,然后解叠,而在亲水性表面上,从一个相邻碱基的解叠先于氢键的完全破坏,然后从第二个相邻碱基上解叠。熔融和杂交的动力学障碍表明,中心碱基在疏水性表面附近迅速熔融,这可以加速构象搜索,从而加速折叠成所需的构象。