Comprehensive Study of Thiazole‐Orange‐Based DNA Dyes

Author:

Domahidy Farkas12ORCID,Kovács Beatrix34,Cseri Levente15ORCID,Katona Gergely6ORCID,Rózsa Balázs167ORCID,Mucsi Zoltán18ORCID,Kovács Ervin59ORCID

Affiliation:

1. BrainVisionCenter Liliom utca 43–45 H-1094 Budapest Hungary

2. Hevesy György PhD School of Chemistry Eötvös Loránd University Pázmány Péter sétány 1/A H-1117 Budapest Hungary

3. Visual Systems Neuroscience Research Group HUN-REN Research Centre for Natural Sciences Magyar tudósok körútja 2 H-1117 Budapest Hungary

4. Semmelweis University Doctoral School Üllői út 26 H-1085 Budapest Hungary

5. Department of Organic Chemistry & Technology Budapest University of Technology & Economics Muegyetem rakpart 3 H-1111 Budapest Hungary

6. Two-Photon Measurement Technology Research Group Pázmány Péter Catholic University Práter utca 50/a H-1083 Budapest Hungary

7. Laboratory of 3D functional network and dendritic imaging HUN-REN Institute of Experimental Medicine Szigony utca 43 H-1083 Budapest Hungary

8. Faculty of Materials and Chemical Sciences University of Miskolc H-3515 Miskolc Hungary

9. Polymer Chemistry and Physics Research Group HUN-REN Research Centre for Natural Sciences Magyar tudósok körútja 2 H-1117 Budapest Hungary

Abstract

AbstractThe 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.

Funder

Nemzeti Kutatási Fejlesztési és Innovációs Hivatal

Nemzeti Kutatási és Technológiai Hivatal

Magyar Tudományos Akadémia

Publisher

Wiley

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