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Force measurements reveal how small binders perturb the dissociation mechanisms of DNA duplex sequences

机译:力测量揭示多小绑定扰乱DNA双螺旋的分离机制序列

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摘要

The force-driven separation of double-stranded DNA is crucial to the accomplishment of cellular processes like genome transactions. Ligands binding to short DNA sequences can have a local stabilizing or destabilizing effect and thus severely affect these processes. Although the design of ligands that bind to specific sequences is a field of intense research with promising biomedical applications, so far, their effect on the force-induced strand separation has remained elusive. Here, by means of AFM-based single molecule force spectroscopy, we show the co-existence of two different mechanisms for the separation of a short DNA duplex and demonstrate how they are perturbed by small binders. With the support of Molecular Dynamics simulations, we evidence that above a critical pulling rate one of the dissociation pathways becomes dominant, with a dramatic effect on the rupture forces. Around the critical threshold, we observe a drop of the most probable rupture forces for ligand-stabilized duplexes. Our results offer a deep understanding of how a stable DNA-ligand complex behaves under force-driven strand separation.
机译:力驱动的双链DNA的分离的成就是至关重要的细胞过程就像基因组的事务。绑定到短DNA序列可以有一个地方从而稳定或不稳定的影响严重影响这些过程。设计的配体结合特定的序列是一个强烈的研究领域有前途吗生物医学应用,到目前为止,他们的影响及链保持分离难以捉摸。分子光谱,我们展示了共存的两个不同的机制短的DNA分离双工和演示他们如何被小摄动绑定。分子动力学模拟的支持,我们证据表明,高于临界拉率离解的途径成为占主导地位的,对断裂部队与一个戏剧性的影响。在临界阈值,我们观察下降最可能的破坏力量ligand-stabilized工器。深刻的理解如何DNA-ligand稳定复杂的行为在力链分离。

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