Visualization of G-quadruplexes in gel and in live cells by a near-infrared fluorescent probe

被引:25
|
作者
Wu, Fan [1 ]
Liu, Chaoxing [1 ]
Chen, Yuqi [1 ]
Yang, Shixi [1 ]
Xu, Jiahui [1 ]
Huang, Rong [3 ]
Wang, Xiang [1 ]
Li, Manjia [1 ]
Liu, Wenting [1 ]
Mao, Wuxiang [2 ]
Zhou, Xiang [1 ]
机构
[1] Wuhan Univ, Minist Educ, Key Lab Biomed Polymers, Coll Chem & Mol Sci, Wuhan 430072, Hubei, Peoples R China
[2] Hubei Univ, Coll Life Sci, Hubei Collaborat Innovat Ctr Green Transformat Bi, Wuhan 430062, Hubei, Peoples R China
[3] South Cent Univ Nationalities, Coll Pharm, Wuhan 430073, Hubei, Peoples R China
来源
基金
美国国家科学基金会;
关键词
Fluorescent probe; G-quadruplex; Direct visualization; Cell imaging; RNA G-QUADRUPLEXES; MESSENGER-RNA; C-MYC; DNA; TELOMERASE; RECOGNITION; SELECTIVITY; AFFINITY; BINDING;
D O I
10.1016/j.snb.2016.05.162
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
G-quadruplexes, one of the most significant secondary structure of nucleic acid, are formed by stacking G quartets, which received broad interests due to their involvement in telomere function, gene transcription and recombination. As for ligand, better selectivity for G-quadruplex against other DNA or RNA structures and higher ability to stabilize G-quadruplex are necessary. In addition, developing a new probe to recognize G-quadruplex is desired for utilizing G-quadruplex structure to relevant biological processes. In this study, we report a Cy5 labelled ligand (named PDP-Cy5) developed as a near-infrared fluorescent ligand for G-quadruplexes both in DNA and RNA. The results indicated that PDP-Cy5 selectively induced the formation of intramolecular G-quadruplexes with strong binding affinity. Furthermore, this Cy5 labelled ligand can effectively stabilize G-quadruplexes. Moreover, the direct visualization of G-quadruplexes in gel, even on cell level is realized by using PDP-Cy5. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:268 / 275
页数:8
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