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源于序列定义障碍的缓慢核酸解链动力学。

Slow nucleic acid unzipping kinetics from sequence-defined barriers.

作者信息

Cocco S, Marko J F, Monasson R

机构信息

CNRS-Laboratoire de Dynamique des Fluides Complexes, 3 rue de l'Université, 67000 Strasbourg, France.

出版信息

Eur Phys J E Soft Matter. 2003 Feb;10(2):153-61. doi: 10.1140/epje/e2003-00019-8.

Abstract

Recent experiments on unzipping of RNA helix-loop structures by force have shown that approximately 40-base molecules can undergo kinetic transitions between two well-defined "open" and "closed" states, on a timescale approximately 1 sec [Liphardt et al., Science 297, 733-737 (2001)]. Using a simple dynamical model, we show that these phenomena result from the slow kinetics of crossing large free energy barriers which separate the open and closed conformations. The dependence of barriers on sequence along the helix, and on the size of the loop(s) is analyzed. Some DNA and RNA sequences that could show dynamics on different time scales, or three(or more)-state unzipping, are proposed. Our dynamical model is also applied to the unzipping of long (kilo-basepair) DNA molecules at constant force.

摘要

最近关于用力解开RNA螺旋-环结构的实验表明,大约40个碱基的分子能够在大约1秒的时间尺度上,在两个明确的“开放”和“封闭”状态之间进行动力学转变[利普哈特等人,《科学》297, 733 - 737 (2001)]。通过一个简单的动力学模型,我们表明这些现象是由跨越分隔开放和封闭构象的大自由能垒的缓慢动力学导致的。分析了能垒对沿着螺旋的序列以及环的大小的依赖性。提出了一些可能在不同时间尺度上表现出动力学,或三(或更多)态解链的DNA和RNA序列。我们的动力学模型也被应用于在恒定力作用下长(千碱基对)DNA分子的解链。

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