Topological effect of an intramolecular split G-quadruplex on thioflavin T binding and fluorescence light-up

被引:4
作者
Lv, Mengmeng [1 ,2 ]
Ren, Jiangtao [2 ]
Wang, Erkang [1 ,2 ]
机构
[1] Jilin Univ, Coll Chem, Changchun 130012, Jilin, Peoples R China
[2] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Electroanalyt Chem, Changchun 130022, Jilin, Peoples R China
基金
中国国家自然科学基金;
关键词
HEPATITIS-B-VIRUS; LABEL-FREE; AMPLIFICATION; VERSATILE;
D O I
10.1039/d3sc06862e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this work, the topological effect on binding interaction between a G-quadruplex and thioflavin T (ThT) ligand was systematically investigated on a platform of an intramolecular split G-quadruplex (Intra-SG). Distinct fluorescence changes from ThT were presented in the presence of distinct split modes of Intra-SG structures and an intriguing phenomenon of target-induced fluorescence light-up occurred for split modes 2 : 10, 5 : 7 and 8 : 4. It was validated that hybridization between the Intra-SG spacer and target did not unfold the G-quadruplex, but facilitated the ThT binding. Moreover, the 3 ' guanine-rich fragment of Intra-SG was very susceptible to topology variation produced by the bound target strand. Additionally, a bioanalytical method was developed for ultrasensitive gene detection, confirming the utility of the ThT/Intra-SG complex as a universal signal transducer. It is believed that the results and disclosed rules will inspire researchers to develop many new DNA-based signal transducers in the future. Hybridization-facilitated thioflavin T (ThT) binding to a G-quadruplex and fluorescence light-up were disclosed on a platform of an intramolecular split G-quadruplex (Intra-SG) and the susceptibility of the 3 ' guanine-rich fragment of Intra-SG was validated.
引用
收藏
页码:4519 / 4528
页数:10
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