Farkas Domahidy, Beatrix Kovács, Dr. Levente Cseri, Dr. Gergely Katona, Dr. Balázs Rózsa, Dr. Zoltán Mucsi, Dr. Ervin Kovács
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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.
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。