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通过力跳跃到一个由熵产生的势垒中。

Hopping around an entropic barrier created by force.

机构信息

Department of Biological Sciences, Columbia University, New York, NY 10027, USA.

出版信息

Biochem Biophys Res Commun. 2010 Dec 3;403(1):133-7. doi: 10.1016/j.bbrc.2010.10.133. Epub 2010 Nov 2.

Abstract

We use Langevin dynamics to investigate the role played by the recently discovered force-induced entropic energy barrier on the two-state hopping phenomena that has been observed in single RNA, DNA and protein molecules placed under a stretching force. Simple considerations about the free energy of a molecule readily show that the application of force introduces an entropic barrier separating the collapsed state of the molecule, from a force-driven extended conformation. A notable characteristic of the force induced barrier is its long distances to transition state, up to tens of nanometers, which renders the kinetics of crossing this barrier highly sensitive to an applied force. Langevin dynamics across such force induced barriers readily demonstrates the hopping behavior observed for a variety of single molecules placed under force. Such hopping is frequently interpreted as a manifestation of two-state folding/unfolding reactions observed in bulk experiments. However, given that such barriers do not exist at zero force these reactions do not take place at all in bulk.

摘要

我们使用朗之万动力学研究了最近发现的力诱导熵能势垒在单 RNA、DNA 和蛋白质分子在拉伸力下观察到的两态跳跃现象中的作用。简单考虑一下分子的自由能,就可以很容易地看出,施加力会引入一个熵势垒,将分子的坍塌状态与力驱动的伸展构象分隔开来。力诱导势垒的一个显著特点是其与过渡态的距离很长,可达数十纳米,这使得跨越该势垒的动力学对施加的力非常敏感。跨越这种力诱导势垒的朗之万动力学很容易证明了在受力下观察到的各种单分子的跳跃行为。这种跳跃经常被解释为在体相实验中观察到的两种状态折叠/展开反应的表现。然而,由于在零力下不存在这样的势垒,这些反应在体相中根本不会发生。

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