Fluorescence assay based on the thioflavin T-induced conformation switch of G-quadruplexes for TET1 detection

被引:9
作者
Chen, Xue [1 ,2 ,3 ]
Cheng, Ying [1 ,2 ]
Wang, Yafen [4 ]
Tang, Jing [1 ,2 ]
Wang, Fang [1 ,2 ,3 ]
Chen, Zilin [1 ,2 ,3 ]
机构
[1] Minist Educ, Key Lab Combinatorial Biosynth & Drug Discovery, Hubei Prov Engn & Technol Res Ctr Fluorinated Pha, Wuhan 430071, Peoples R China
[2] Wuhan Univ, Sch Pharmaceut Sci, Wuhan 430071, Peoples R China
[3] Chinese Acad Sci, State Key Lab Of1tansducer Technol, Beijing 100080, Peoples R China
[4] Wuhan Univ, Key Lab Biochem Polymers Minist Educ, Coll Chem & Mol Sci, Hubei Prov Key Lab Allergy & Immunol,Inst Adv Stu, Wuhan 430072, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
ALKALINE-PHOSPHATASE ACTIVITY; DNA; DNAZYMES; ENZYMES; SENSOR;
D O I
10.1039/d1an00109d
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Ten-eleven translocation (TET) dioxygenase is of great significance in cytosine demethylation and in the control of cell differentiation and transformation. Herein, a fluorescence method has been developed for the highly sensitive detection of TET1, a member of the TET dioxygenase family. Based on the ThT-induced specific conformation of the G-quadruplex structure, the fluorescence signal decreased linearly with increasing TET1 concentration. The method shows potential clinical applications in the screening of TET protein inhibitors for anticancer drug discovery.
引用
收藏
页码:2126 / 2130
页数:5
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