PREDICTED EFFECTS OF LOCAL CONFORMATIONAL COUPLING AND EXTERNAL RESTRAINTS ON THE TORSIONAL PROPERTIES OF SINGLE DNA MOLECULES.

IF 16.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Atsushi Matsumoto, Wilma K Olson
{"title":"PREDICTED EFFECTS OF LOCAL CONFORMATIONAL COUPLING AND EXTERNAL RESTRAINTS ON THE TORSIONAL PROPERTIES OF SINGLE DNA MOLECULES.","authors":"Atsushi Matsumoto,&nbsp;Wilma K Olson","doi":"10.1137/060663040","DOIUrl":null,"url":null,"abstract":"<p><p>A newly developed, coarse-grained treatment of the low-frequency normal modes of DNA has been adapted to study the torsional properties of fully extended, double-helical molecules. Each base pair is approximated in this scheme as a rigid body, and molecular structure is described in terms of the relative position and orientation of successive base pairs. The torsional modulus C is computed from the lowest-frequency normal twisting mode using expressions valid for a homogeneous, naturally straight elastic rod. Fluctuations of local dimeric structure, including the coupled variation of conformational parameters, are based on the observed arrangements of neighboring base pairs in high-resolution structures. Chain ends are restrained by an elastic energy term. The calculations show how the end-to-end constraints placed on a naturally straight DNA molecule, in combination with the natural conformational features of the double helix, can account for the substantially larger torsional moduli determined with state-of-the-art, single-molecule experiments compared to values extracted from solution measurements and/or incorporated into theories to account for the force-extension properties of single molecules. The computed normal-mode frequencies and torsional moduli increase substantially if base pairs are inclined with respect to the double-helical axis and the deformations of selected conformational variables follow known interdependent patterns. The changes are greatest if the fluctuations in dimeric twisting are coupled with parameters that directly alter the end-to-end displacement. Imposed restraints that mimic the end-to-end conditions of single-molecule experiments then impede the twisting of base pairs and increase the torsional modulus. The natural inclination of base pairs concomitantly softens the Young's modulus, i.e., ease of duplex stretching. The analysis of naturally curved DNA points to a drop in the torsional modulus upon imposed extension of the double-helical molecule.</p>","PeriodicalId":1,"journal":{"name":"Accounts of Chemical Research","volume":null,"pages":null},"PeriodicalIF":16.4000,"publicationDate":"2006-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1137/060663040","citationCount":"4","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Accounts of Chemical Research","FirstCategoryId":"100","ListUrlMain":"https://doi.org/10.1137/060663040","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 4

Abstract

A newly developed, coarse-grained treatment of the low-frequency normal modes of DNA has been adapted to study the torsional properties of fully extended, double-helical molecules. Each base pair is approximated in this scheme as a rigid body, and molecular structure is described in terms of the relative position and orientation of successive base pairs. The torsional modulus C is computed from the lowest-frequency normal twisting mode using expressions valid for a homogeneous, naturally straight elastic rod. Fluctuations of local dimeric structure, including the coupled variation of conformational parameters, are based on the observed arrangements of neighboring base pairs in high-resolution structures. Chain ends are restrained by an elastic energy term. The calculations show how the end-to-end constraints placed on a naturally straight DNA molecule, in combination with the natural conformational features of the double helix, can account for the substantially larger torsional moduli determined with state-of-the-art, single-molecule experiments compared to values extracted from solution measurements and/or incorporated into theories to account for the force-extension properties of single molecules. The computed normal-mode frequencies and torsional moduli increase substantially if base pairs are inclined with respect to the double-helical axis and the deformations of selected conformational variables follow known interdependent patterns. The changes are greatest if the fluctuations in dimeric twisting are coupled with parameters that directly alter the end-to-end displacement. Imposed restraints that mimic the end-to-end conditions of single-molecule experiments then impede the twisting of base pairs and increase the torsional modulus. The natural inclination of base pairs concomitantly softens the Young's modulus, i.e., ease of duplex stretching. The analysis of naturally curved DNA points to a drop in the torsional modulus upon imposed extension of the double-helical molecule.

预测局部构象耦合和外部约束对单个DNA分子扭转特性的影响。
一种新开发的,对DNA的低频正常模式的粗粒度处理已经适应于研究完全扩展的双螺旋分子的扭转特性。每个碱基对在该方案中近似为一个刚体,分子结构是根据连续碱基对的相对位置和取向来描述的。扭转模量C是从最低频率的正态扭转模式计算的,使用适用于均匀的自然直弹性杆的表达式。局部二聚体结构的波动,包括构象参数的耦合变化,是基于观察到的高分辨率结构中相邻碱基对的排列。链的末端受到弹性能项的约束。计算表明,与从溶液测量中提取的值相比,放置在自然直DNA分子上的端到端约束,结合双螺旋的自然构象特征,可以解释用最先进的单分子实验确定的更大的扭转模量,并且/或纳入理论来解释单分子的力扩展特性。如果碱基对相对于双螺旋轴倾斜,并且选定构象变量的变形遵循已知的相互依赖模式,则计算出的正模态频率和扭转模量将大幅增加。如果二聚体扭转的波动与直接改变端到端位移的参数相耦合,则变化最大。施加的约束模拟了单分子实验的端到端条件,然后阻碍了碱基对的扭曲并增加了扭转模量。碱基对的自然倾斜同时软化了杨氏模量,即易于双相拉伸。对自然弯曲的DNA的分析表明,双螺旋分子的拉伸会导致扭转模量的下降。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Accounts of Chemical Research
Accounts of Chemical Research 化学-化学综合
CiteScore
31.40
自引率
1.10%
发文量
312
审稿时长
2 months
期刊介绍: Accounts of Chemical Research presents short, concise and critical articles offering easy-to-read overviews of basic research and applications in all areas of chemistry and biochemistry. These short reviews focus on research from the author’s own laboratory and are designed to teach the reader about a research project. In addition, Accounts of Chemical Research publishes commentaries that give an informed opinion on a current research problem. Special Issues online are devoted to a single topic of unusual activity and significance. Accounts of Chemical Research replaces the traditional article abstract with an article "Conspectus." These entries synopsize the research affording the reader a closer look at the content and significance of an article. Through this provision of a more detailed description of the article contents, the Conspectus enhances the article's discoverability by search engines and the exposure for the research.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信