A small-sized benzothiazole-indolium fluorescent probe: the study of interaction specificity targeting c-MYC promoter G-quadruplex structures and live cell imaging

被引:23
作者
Zheng, Bo-Xin [1 ]
She, Meng-Ting [1 ]
Long, Wei [1 ]
Xu, Yong-Yu [1 ]
Zhang, Yi-Han [1 ]
Huang, Xuan-He [1 ]
Liu, Wenjie [3 ,4 ]
Hou, Jin-Qiang [3 ,4 ]
Wong, Wing-Leung [2 ,5 ]
Lu, Yu-Jing [1 ]
机构
[1] Guangdong Univ Technol, Sch Biomed & Pharmaceut Sci, Guangzhou 510006, Peoples R China
[2] Hong Kong Polytech Univ, Dept Appl Biol Chem Technol, State Key Lab Chem Biol & Drug Discovery, Hung Hom,Kowloon, Hong Kong, Peoples R China
[3] Lakehead Univ, Dept Chem, 980 Oliver Rd, Thunder Bay, ON P7B 6V4, Canada
[4] Thunder Bay Reg Hlth Res Inst, 980 Oliver Rd, Thunder Bay, ON P7B 6V4, Canada
[5] Wuyi Univ, Sch Biotechnol & Hlth Sci, Jiangmen 529020, Peoples R China
关键词
SMALL-MOLECULE; THIOFLAVIN T; DNA;
D O I
10.1039/d0cc06525k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A small-sized c-MYC promoter G-quadruplex selective fluorescent BZT-Indolium binding ligand was demonstrated for the first time as a highly target-specific and photostable probe for in vitro staining and live cell imaging and it was found to be able to inhibit the amplification of the c-MYC G-rich sequence (G-quadruplex) and down-regulate oncogene c-MYC expression in human cancer cells (HeLa).
引用
收藏
页码:15016 / 15019
页数:4
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