Faculty of Systems Engineering, Wakayama University, 930 Sakaedani, Wakayama, 640-8510, Japan.
Chembiochem. 2019 May 15;20(10):1242-1245. doi: 10.1002/cbic.201800738. Epub 2019 Mar 26.
A new label-free in situ monitoring system for the hybridization chain reaction (HCR) based on DNA minor-groove-binding fluorophores [Hoechst 33258 (Hoe) or quinone cyanine-dithiazole (QCy-DT)] has been developed. Use of two unmodified hairpin oligodeoxyribonucleotides containing incomplete double-stranded AATT sequences enabled target-dependent formation of probe binding sites-that is, AATT double strand-in the HCR product, together with fluorescence enhancement of minor-groove-binding fluorophores in situ. This system allows target DNA to be detected through the fluorescence enhancement of Hoe and QCy-DT in real time and in situ. Further development of a label-free, isothermal detection system might provide a cost-effective and user-friendly method for nucleic acid detection.
一种新的基于 DNA 小沟结合荧光染料(Hoechst 33258(Hoe)或醌氰基二噻唑(QCy-DT))的杂交链反应(HCR)的无标记原位监测系统已经开发出来。使用两个含有不完整双链 AATT 序列的未修饰发夹寡脱氧核苷酸,使得能够在 HCR 产物中形成依赖于靶标的探针结合位点,即 AATT 双链,同时原位增强小沟结合荧光染料的荧光。该系统允许通过实时和原位的 Hoe 和 QCy-DT 荧光增强来检测靶 DNA。进一步开发无标记、等温检测系统可能为核酸检测提供一种具有成本效益和用户友好的方法。