Effects of Mg2+ and ATP on YOYO-1 labeling of genomic DNA in single molecule experiments

IF 2.2 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Carl Möller , Dennis Winter , Radhika Nambannor Kunnath, Sriram KK, Fredrik Westerlund
{"title":"Effects of Mg2+ and ATP on YOYO-1 labeling of genomic DNA in single molecule experiments","authors":"Carl Möller ,&nbsp;Dennis Winter ,&nbsp;Radhika Nambannor Kunnath,&nbsp;Sriram KK,&nbsp;Fredrik Westerlund","doi":"10.1016/j.bbrep.2025.102248","DOIUrl":null,"url":null,"abstract":"<div><div>Nanofluidic channels have emerged as a suitable tool to study DNA-protein interactions. Many DNA-interacting proteins require ATP to fully function and use Mg<sup>2+</sup> as a cofactor. Mg<sup>2+</sup> and ATP are however also known to influence the binding of dyes, such as the commonly used YOYO-1, to DNA. This study investigates the effects of Mg<sup>2+</sup> ions and ATP on YOYO-1 labeled genomic DNA and shows, via single molecule experiments in nanochannels, that Mg<sup>2+</sup> reduces the fluorescence intensity of YOYO-1 labeled DNA, as well as the extension of the DNA, at both low and high dye loadings. When combined, ATP counteracts the loss of fluorescence caused by Mg<sup>2+</sup>, but only at comparable concentrations. Additionally, while increasing the photobleaching rate, Mg<sup>2+</sup> delays dye-mediated photolytic DNA damage, reducing DNA fragmentation in the nanofluidic channels. Determination of the apparent binding constant by bulk measurements corroborates the single molecule observations, suggesting that Mg<sup>2+</sup> causes dissociation of YOYO-1 from DNA. These findings demonstrate that the addition of Mg<sup>2+</sup> and ATP poses challenges in DNA-protein studies using nanofluidics, which can be mitigated by optimizing experimental conditions.</div></div>","PeriodicalId":8771,"journal":{"name":"Biochemistry and Biophysics Reports","volume":"44 ","pages":"Article 102248"},"PeriodicalIF":2.2000,"publicationDate":"2025-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biochemistry and Biophysics Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2405580825003358","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Nanofluidic channels have emerged as a suitable tool to study DNA-protein interactions. Many DNA-interacting proteins require ATP to fully function and use Mg2+ as a cofactor. Mg2+ and ATP are however also known to influence the binding of dyes, such as the commonly used YOYO-1, to DNA. This study investigates the effects of Mg2+ ions and ATP on YOYO-1 labeled genomic DNA and shows, via single molecule experiments in nanochannels, that Mg2+ reduces the fluorescence intensity of YOYO-1 labeled DNA, as well as the extension of the DNA, at both low and high dye loadings. When combined, ATP counteracts the loss of fluorescence caused by Mg2+, but only at comparable concentrations. Additionally, while increasing the photobleaching rate, Mg2+ delays dye-mediated photolytic DNA damage, reducing DNA fragmentation in the nanofluidic channels. Determination of the apparent binding constant by bulk measurements corroborates the single molecule observations, suggesting that Mg2+ causes dissociation of YOYO-1 from DNA. These findings demonstrate that the addition of Mg2+ and ATP poses challenges in DNA-protein studies using nanofluidics, which can be mitigated by optimizing experimental conditions.
Mg2+和ATP对基因组DNA YOYO-1标记的单分子实验影响
纳米流体通道已成为研究dna -蛋白质相互作用的合适工具。许多dna相互作用蛋白需要ATP才能充分发挥作用,并使用Mg2+作为辅助因子。然而,已知Mg2+和ATP也会影响染料(如常用的YOYO-1)与DNA的结合。本研究探讨了Mg2+离子和ATP对YOYO-1标记的基因组DNA的影响,并通过纳米通道的单分子实验表明,在低和高染料负载下,Mg2+降低了YOYO-1标记DNA的荧光强度,以及DNA的延伸。当结合时,ATP抵消了Mg2+引起的荧光损失,但仅在相当浓度下。此外,在增加光漂白速率的同时,Mg2+延缓了染料介导的光解DNA损伤,减少了纳米流体通道中DNA的断裂。通过体积测量测定表观结合常数证实了单分子观察结果,表明Mg2+导致YOYO-1与DNA分离。这些发现表明,Mg2+和ATP的加入对使用纳米流体进行dna -蛋白质研究提出了挑战,可以通过优化实验条件来缓解这一挑战。
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
Biochemistry and Biophysics Reports
Biochemistry and Biophysics Reports Biochemistry, Genetics and Molecular Biology-Biophysics
CiteScore
4.60
自引率
0.00%
发文量
191
审稿时长
59 days
期刊介绍: Open access, online only, peer-reviewed international journal in the Life Sciences, established in 2014 Biochemistry and Biophysics Reports (BB Reports) publishes original research in all aspects of Biochemistry, Biophysics and related areas like Molecular and Cell Biology. BB Reports welcomes solid though more preliminary, descriptive and small scale results if they have the potential to stimulate and/or contribute to future research, leading to new insights or hypothesis. Primary criteria for acceptance is that the work is original, scientifically and technically sound and provides valuable knowledge to life sciences research. We strongly believe all results deserve to be published and documented for the advancement of science. BB Reports specifically appreciates receiving reports on: Negative results, Replication studies, Reanalysis of previous datasets.
×
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