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小型DNA质粒的分子动力学模拟:序列和超螺旋对分子内运动的影响

Molecular dynamics simulations of small DNA plasmids: effects of sequence and supercoiling on intramolecular motions.

作者信息

Tan R K, Sprous D, Harvey S C

机构信息

Department of Biochemistry and Molecular Genetics, University of Alabama at Birmingham 35205-0005, USA.

出版信息

Biopolymers. 1996 Aug;39(2):259-78. doi: 10.1002/(sici)1097-0282(199608)39:2<259::aid-bip12>3.0.co;2-9.

DOI:10.1002/(sici)1097-0282(199608)39:2<259::aid-bip12>3.0.co;2-9
PMID:8679953
Abstract

Small (600 base pair) DNA plasmids were modeled with a simplified representation (3DNA) and the intramolecular motions were studied using molecular mechanics and molecular dynamics techniques. The model is detailed enough to incorporate sequence effects. At the same time, it is simple enough to allow long molecular dynamics simulations. The simulations revealed that large-scale slithering occurs in a homogeneous sequence. In a heterogeneous sequence, containing numerous small intrinsic curves, the centers of the curves are preferentially positioned at the tips of loops. With more curves than loop tips (two in unbranched supercoiled DNA), the heterogeneous sequence plasmid slithers short distances to reposition other curves into the loop tips. However, the DNA is immobilized most of the time, with the loop tips positioned over a few favored curve centers. Branching or looping also appears in the heterogeneous sequence as a new method of repositioning the loop tips. Instead of a smooth progression of increasing writhing with increasing linking difference, theoretical studies have predicted that there is a threshold between unwrithed and writhed DNA at a linking difference between one and two. This has previously been observed in simulations of static structures and is demonstrated here for dynamic homogeneous closed DNA. Such an abrupt transition is not found in the heterogeneous sequence in both the static and dynamic cases.

摘要

小型(600个碱基对)DNA质粒采用简化表示法(3DNA)进行建模,并使用分子力学和分子动力学技术研究其分子内运动。该模型足够详细,可以纳入序列效应。同时,它又足够简单,能够进行长时间的分子动力学模拟。模拟结果表明,在均匀序列中会发生大规模的滑动。在包含许多小的固有曲线的异质序列中,曲线的中心优先位于环的末端。由于曲线比环末端多(在无分支的超螺旋DNA中有两个),异质序列质粒会短距离滑动,将其他曲线重新定位到环末端。然而,DNA大部分时间是固定的,环末端位于几个有利的曲线中心上方。分支或成环在异质序列中也作为重新定位环末端的一种新方法出现。理论研究预测,与随着连接差增加而逐渐增加的扭曲不同,在连接差为1到2之间时,未扭曲和扭曲的DNA之间存在一个阈值。这一点此前在静态结构模拟中已经观察到,此处则在动态均匀封闭DNA中得到了证明。在静态和动态情况下,异质序列中均未发现这种突然转变。

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Molecular dynamics simulations of small DNA plasmids: effects of sequence and supercoiling on intramolecular motions.小型DNA质粒的分子动力学模拟:序列和超螺旋对分子内运动的影响
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