Triphenylmethane dyes as fluorescent probes for G-quadruplex recognition

被引:49
作者
Guo, Jun-Hong [2 ]
Zhu, Li-Na [3 ]
Kong, De-Ming [1 ,2 ]
Shen, Han-Xi [2 ]
机构
[1] Nankai Univ, Key Lab Funct Polymer Mat, Minist Educ, Tianjin 300071, Peoples R China
[2] Nankai Univ, Dept Chem, Res Ctr Analyt Sci, Tianjin 300071, Peoples R China
[3] Tianjin Univ, Dept Chem, Tianjin 300072, Peoples R China
基金
中国国家自然科学基金;
关键词
Fluorescent probe; Triphenylmethane dye; G-quadruplex; Double-stranded DNA; Single-stranded DNA; C-MYC PROMOTER; DNA STRUCTURES; SMALL-MOLECULE; BINDING; TELOMERASE; INHIBITION; REGION;
D O I
10.1016/j.talanta.2009.07.034
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Triphenylmethane (TPM) dyes normally render rather weak fluorescence due to easy vibrational deexcitation. However, when they stack onto the two external G-quartets of a G-quadruplex (especially intramolecular G-quadruplex), such vibrations will be restricted, resulting in greatly enhanced fluorescence intensities. Thus, TPM dyes may be developed as sensitive G-quadruplex fluorescent probes. Here, fluorescence spectra and energy transfer spectra of five TPM dyes in the presence of G-quadruplexes, single- or double-stranded DNAs were compared. The results show that the fluorescence spectra of four TPM dyes can be used to discriminate intramolecular G-quadruplexes from intermolecular G-quadruplexes, single- and double-stranded DNAs. The energy transfer fluorescence spectra and energy transfer fluorescence titration can be used to distinguish G-quadruplexes (including intramolecular and intermolecular G-quadruplexes) from single- and double-stranded DNAs. Positive charges and substituent size in TPM dyes may be two important factors in influencing the binding stability of the dyes and G-quadruplexes. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:607 / 613
页数:7
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