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高盐浓度介质中 Drew-Dickerson DNA 的变性:分子动力学模拟。

Denaturation of Drew-Dickerson DNA in a high salt concentration medium: molecular dynamics simulations.

机构信息

Department of Chemistry, Sharif University of Technology, Tehran, Iran.

出版信息

J Comput Chem. 2011 Dec;32(16):3354-61. doi: 10.1002/jcc.21908. Epub 2011 Sep 20.

Abstract

We have performed molecular dynamics simulation on B-DNA duplex (CGCGAATTGCGC) at different temperatures. The DNA was immerged in a salt-water medium with 1 M NaCl concentration to investigate salt effect on the denaturation process. At each temperature, configurational entropy is estimated using the covariance matrix of atom-positional fluctuations, from which the melting temperature (T(m)) was found to be 349 K. The calculated configuration entropy for different bases shows that the melting process involves more peeling (including fraying from the ends) conformations, and therefore the untwisting of the duplex and peeling states form the transition state of the denaturation process. There is a narrow minor groove in the AATT sequence that becomes wider by increasing temperature which disappears at high temperatures, especially above the melting temperature. We have also calculated the fraction of denatured base pairs, f-curve, from which T(m) was found to be 340 K, close to experimental value of 341 K. We found that DNA at high salt concentrations has few hydrogen bonds even at temperatures higher than the T(m). Our calculations show the fact that adding salt leads to increase of T(m) and stabilization of DNA.

摘要

我们在不同温度下对 B-DNA 双链(CGCGAATTGCGC)进行了分子动力学模拟。将 DNA 浸入含有 1 M NaCl 浓度的盐水中,以研究盐对变性过程的影响。在每个温度下,使用原子位置波动的协方差矩阵估计构象熵,由此发现熔点(Tm)为 349 K。对不同碱基的计算构象熵表明,熔化过程涉及更多的剥离(包括从末端开始的剥落)构象,因此双链体的解旋和剥落状态形成了变性过程的过渡态。在 AATT 序列中有一个狭窄的小沟,随着温度的升高而变宽,在高温下消失,尤其是在熔点以上。我们还计算了变性碱基对的分数,f-曲线,由此发现 Tm 为 340 K,接近实验值 341 K。我们发现,即使在高于 Tm 的温度下,高盐浓度的 DNA 也很少有氢键。我们的计算表明,加盐会导致 Tm 升高和 DNA 稳定。

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