Comprehensive Study of Thiazole-Orange-Based DNA Dyes

IF 3 4区 化学 Q3 CHEMISTRY, PHYSICAL
Farkas Domahidy, Beatrix Kovács, Dr. Levente Cseri, Dr. Gergely Katona, Dr. Balázs Rózsa, Dr. Zoltán Mucsi, Dr. Ervin Kovács
{"title":"Comprehensive Study of Thiazole-Orange-Based DNA Dyes","authors":"Farkas Domahidy,&nbsp;Beatrix Kovács,&nbsp;Dr. Levente Cseri,&nbsp;Dr. Gergely Katona,&nbsp;Dr. Balázs Rózsa,&nbsp;Dr. Zoltán Mucsi,&nbsp;Dr. Ervin Kovács","doi":"10.1002/cptc.202400080","DOIUrl":null,"url":null,"abstract":"<p>The rapid advancement of biotechnology over the recent decades has amplified the importance of DNA detection and quantification assays. Many of these assays, such as gel electrophoresis, microscopy, flow cytometry, and the detection of amplification in quantitative polymerase chain reaction (qPCR), rely on the use of DNA-binding fluorescent dyes. This article presents a comprehensive study of six Thiazole-Orange-based fluorescent DNA-binding dyes: SYBR Safe, SYBR Green, Pico Green, SYTO-16, SYTO-9, and the benzothiazole-based analogue (TOPhBu) of the latter. The selected DNA markers were synthesized at a 10-milligram scale and characterised spectroscopically to quantify their fluorescence enhancement upon binding to double-stranded DNA. The ability of the dyes to detect DNA at low concentrations was evaluated using two new metrics, absolute fluorescence enhancement (AFE) and relative fluorescence enhancement (RFE). Quantum chemical calculations shed new light on the mechanism of their fluorogenicity through modelling the excited state behaviour and DNA binding of the dyes. Their analytical performance was further tested in qPCR experiments. The experimental results of this work highlight some important differences in the sensitivity and qPCR efficiency of the studied DNA-binding dyes which will facilitate the DNA marker selection for analytical purposes and the future development of novel DNA sensors.</p>","PeriodicalId":10108,"journal":{"name":"ChemPhotoChem","volume":"8 10","pages":""},"PeriodicalIF":3.0000,"publicationDate":"2024-05-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cptc.202400080","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemPhotoChem","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cptc.202400080","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

Abstract

The rapid advancement of biotechnology over the recent decades has amplified the importance of DNA detection and quantification assays. Many of these assays, such as gel electrophoresis, microscopy, flow cytometry, and the detection of amplification in quantitative polymerase chain reaction (qPCR), rely on the use of DNA-binding fluorescent dyes. This article presents a comprehensive study of six Thiazole-Orange-based fluorescent DNA-binding dyes: SYBR Safe, SYBR Green, Pico Green, SYTO-16, SYTO-9, and the benzothiazole-based analogue (TOPhBu) of the latter. The selected DNA markers were synthesized at a 10-milligram scale and characterised spectroscopically to quantify their fluorescence enhancement upon binding to double-stranded DNA. The ability of the dyes to detect DNA at low concentrations was evaluated using two new metrics, absolute fluorescence enhancement (AFE) and relative fluorescence enhancement (RFE). Quantum chemical calculations shed new light on the mechanism of their fluorogenicity through modelling the excited state behaviour and DNA binding of the dyes. Their analytical performance was further tested in qPCR experiments. The experimental results of this work highlight some important differences in the sensitivity and qPCR efficiency of the studied DNA-binding dyes which will facilitate the DNA marker selection for analytical purposes and the future development of novel DNA sensors.

Abstract Image

噻唑-橙基 DNA 染料的综合研究
过去几十年来,生物技术突飞猛进,使 DNA 检测和定量测定变得更加重要。其中许多检测方法,如凝胶电泳、显微镜、流式细胞术和定量聚合酶链式反应(qPCR)中的扩增检测,都依赖于 DNA 结合荧光染料的使用。本文全面研究了六种基于噻唑-橙的 DNA 结合荧光染料:SYBR Safe、SYBR Green、Pico Green、SYTO-16、SYTO-9 以及后者的苯并噻唑基类似物(TOPhBu)。所选 DNA 标记的合成量为 10 毫克级,并通过光谱分析确定其与双链 DNA 结合后荧光增强的程度。利用绝对荧光增强(AFE)和相对荧光增强(RFE)这两个新指标评估了染料在低浓度下检测 DNA 的能力。量子化学计算通过模拟染料的激发态行为和 DNA 结合情况,对染料的致氟机理有了新的认识。它们的分析性能在 qPCR 实验中得到了进一步检验。这项工作的实验结果凸显了所研究的 DNA 结合染料在灵敏度和 qPCR 效率方面的一些重要差异,这将有助于选择用于分析目的的 DNA 标记和未来新型 DNA 传感器的开发。
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
ChemPhotoChem
ChemPhotoChem Chemistry-Physical and Theoretical Chemistry
CiteScore
5.80
自引率
5.40%
发文量
165
×
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