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Double-Stranded DNA Dissociates into Single Strands When Dragged into a Poor Solvent

机译:当拖入不良溶剂中时,双链DNA分解成单链

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DNA displays a richness of biologically relevant supramolecular structures, which depend on both sequence and ambient conditions. The effect of dragging double-stranded DNA (dsDNA) from water into poor solvent on the double-stranded structure is still unclear because of condensation. Here, we employed single molecule techniques based on atomic force microscopy and molecular dynamics (MD) simulations to investigate the change in structure and mechanics of DNA during the ambient change. We found that the two strands are split apart when the dsDNA is pulled at one strand from water into a poor solvent. The findings were corroborated by MD simulations where dsDNA was dragged from water into poor solvent, revealing details of the strand separation at the water/poor solvent interface. Because the structure of DNA is of high polarity, all poor solvents show a relatively low polarity. We speculate that the principle of spontaneous unwinding/splitting of dsDNA by providing a low-polarity (in other word, hydrophobic) micro-environment is exploited as one of the catalysis mechanisms of helicases.
机译:DNA显示出丰富的生物学相关超分子结构,这取决于序列和环境条件。由于缩合,从水中将双链DNA(dsDNA)拖入不良溶剂中对双链结构的影响仍然不清楚。在这里,我们采用基于原子力显微镜和分子动力学(MD)模拟的单分子技术来研究环境变化期间DNA的结构和力学变化。我们发现,当将dsDNA从水中的一条链中拉入不良溶剂中时,两条链会分开。 MD模拟证实了该发现,其中将dsDNA从水中拖入不良溶剂中,揭示了水/不良溶剂界面处链分离的细节。由于DNA的结构具有高极性,因此所有不良溶剂均显示相对较低的极性。我们推测通过提供低极性(换句话说,疏水性)微环境而自发解链/分裂dsDNA的原理被用作解旋酶的催化机制之一。

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