A G-triplex-Based Label-Free Fluorescence Switching Platform for the Specific Recognition of Chromium Species

荧光 折叠(DSP实现) 生物传感器 化学 DNA 合理设计 纳米技术 材料科学 拓扑(电路) 物理 生物化学 量子力学 组合数学 电气工程 工程类 数学 有机化学
作者
Qiusha Li,Shuzhen Peng,Yun Chang,Mujing Yang,Dandan Wang,Xiaoshun Zhou,Yong Shao
出处
期刊:Journal of Photochemistry and Photobiology A-chemistry [Elsevier]
卷期号:: 114071-114071
标识
DOI:10.1016/j.jphotochem.2022.114071
摘要

A HtG3 fluorescent switching sensing platform for Cr 3+ qualitative identification based on binding-induced G3 structural breaking and COR fluorescence recovery. • A G-triplex (HtG3) fluorescence switch-on sensor was constructed for metal-ion (Cr 3+ ) qualitative identification. • A fluorescence label-free method based on the competitive binding of COR and Cr 3+ with HtG3. • The structural flexibility and tunability of HtG3 contributed to its better performance on Cr 3+ responsing. • This report extended the practical application of G3 in the sensing fields. G-triplex (G3), as an intermediate of G-quardruplex (G4), is a typical non-classical DNA topology with three G-tracts, formed by folding guanine-riched DNA sequences. The flexibility and tunability of G3-folding structures can provide a versatile platform for analytes sensing. However, current researches about G3s on sensing applications, especially on metal ion sensing, are relatively rare. Herein, we first develop a label-free fluorescence switch-on sensing platform based on the G-triplex topology (HtG3) for the specific qualitative identification of chromium species. Coralyne (COR), a molecule probe whose fluorescence can be inhibited by HtG3, is employed to monitor the Cr 3+ binding events with the principle that Cr 3+ could break the parallel HtG3-folding structure to result in COR releasing from HtG3 and its fluorescence recovery. Furthermore, this HtG3 sensing platform we constructed also can be used to indirectly identify CrO 4 2- through reducing it to Cr 3+ with ascorbic acid (AA). Our work will extend the practical application of G3 as a biosensor and inspire wide interests in exploring more non-classical DNA structures.
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