Assessment of dynamic disorder in DNA oligonucleotides using low-frequency Raman spectroscopy

A.Y. Sosorev, O. D. Parashchuk, A. A. Trubitsyn, N.O. Dubinets, I.V. Chicherin, D. Paraschuk
{"title":"Assessment of dynamic disorder in DNA oligonucleotides using low-frequency Raman spectroscopy","authors":"A.Y. Sosorev, O. D. Parashchuk, A. A. Trubitsyn, N.O. Dubinets, I.V. Chicherin, D. Paraschuk","doi":"10.55959/msu0579-9392.79.2420402","DOIUrl":null,"url":null,"abstract":"The degree of DNA compaction in various regions of the cell nucleus determines whether the corresponding\ngenes should be expressed, and whether other important cellular processes, such as DNA replication and repair,\nshould take place. However, approaches to the experimental assessment of the compactness of DNA in cell\nnuclei, as well as its indicator, dynamic disorder — thermal fluctuations in the position and mutual orientation\nof molecular fragments — are practically not developed. In this paper, using single-stranded oligonucleotides\nguanine and cytosine, as well as their double-stranded combination as an example, we show that dynamic\ndisorder in DNA can be estimated using low-frequency Raman spectroscopy. For the first time, the Raman\nspectra of oligonucleotides were measured in a wide range including the low-frequency and high-frequency\nregions. It was found that the low-frequency Raman intensity is maximal for single-stranded oligocytosine\nand minimal in double-stranded oligonucleotide, in full agreement with the magnitude of dynamic disorder\nestimated from the molecular dynamics simulations. The results obtained indicate the prospects of using\nlow-frequency Raman spectroscopy to assess the dynamic disorder and compactness of DNA. It is expected\nthat the use of such a technique should contribute to the understanding of key cellular processes and their\nunderlying physical mechanisms, which is necessary for the development of advanced methods of molecular\nbiophysics and cell biology.","PeriodicalId":399279,"journal":{"name":"Seriya 3: Fizika, Astronomiya","volume":"12 19","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-05-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Seriya 3: Fizika, Astronomiya","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.55959/msu0579-9392.79.2420402","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

The degree of DNA compaction in various regions of the cell nucleus determines whether the corresponding genes should be expressed, and whether other important cellular processes, such as DNA replication and repair, should take place. However, approaches to the experimental assessment of the compactness of DNA in cell nuclei, as well as its indicator, dynamic disorder — thermal fluctuations in the position and mutual orientation of molecular fragments — are practically not developed. In this paper, using single-stranded oligonucleotides guanine and cytosine, as well as their double-stranded combination as an example, we show that dynamic disorder in DNA can be estimated using low-frequency Raman spectroscopy. For the first time, the Raman spectra of oligonucleotides were measured in a wide range including the low-frequency and high-frequency regions. It was found that the low-frequency Raman intensity is maximal for single-stranded oligocytosine and minimal in double-stranded oligonucleotide, in full agreement with the magnitude of dynamic disorder estimated from the molecular dynamics simulations. The results obtained indicate the prospects of using low-frequency Raman spectroscopy to assess the dynamic disorder and compactness of DNA. It is expected that the use of such a technique should contribute to the understanding of key cellular processes and their underlying physical mechanisms, which is necessary for the development of advanced methods of molecular biophysics and cell biology.
利用低频拉曼光谱评估 DNA 寡核苷酸的动态无序性
细胞核各区域 DNA 的致密程度决定了相应基因是否应该表达,以及其他重要的细胞过程(如 DNA 复制和修复)是否应该进行。然而,对细胞核中 DNA 的致密性及其指标--动态无序(分子片段位置和相互取向的热波动)--进行实验评估的方法实际上并不成熟。本文以单链寡核苷酸鸟嘌呤和胞嘧啶以及它们的双链组合为例,展示了利用低频拉曼光谱可以估算 DNA 的动态无序性。我们首次在包括低频和高频区域在内的宽范围内测量了寡核苷酸的拉曼光谱。研究发现,单链寡核苷酸的低频拉曼光谱强度最大,而双链寡核苷酸的拉曼光谱强度最小,这与分子动力学模拟估计的动态失调幅度完全一致。研究结果表明,利用低频拉曼光谱评估 DNA 的动态无序度和紧密度具有广阔的前景。预计这种技术的使用将有助于理解关键的细胞过程及其基本物理机制,这对于开发先进的分子生物物理学和细胞生物学方法是必要的。
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
自引率
0.00%
发文量
0
×
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:604180095
Book学术官方微信