Spectroscopic study one thiosemicarbazone derivative with ctDNA using ethidium bromide as a fluorescence probe

被引:31
作者
Geng, Shaoguang [1 ]
Wu, Qing [2 ]
Shi, Lei [1 ]
Cui, Fengling [1 ]
机构
[1] Henan Normal Univ, Sch Chem & Chem Engn, Xinxiang 453007, Peoples R China
[2] Henan Normal Univ, Sch Environm, Xinxiang 453007, Peoples R China
基金
中国国家自然科学基金;
关键词
(E)-2-((1,4-dihydroxy-9,10-anthraquinone-2-yl) methylene)-N-(4-fluorophenyl); hydrazinecarbothioamide (DAFPT); Calf thymus DNA (ctDNA); Ethidium bromide (EB); Fluorescence spectroscopy; Molecular docking; NEUTRAL RED-DYE; ACRIDINE-ORANGE; DNA INTERACTION; SYNCHRONOUS FLUORESCENCE; INTERACTION MECHANISM; COMPLEX; BINDING; FLAVONOIDS; BLUE;
D O I
10.1016/j.ijbiomac.2013.06.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In this study, a thiosemicarbazone derivative (E)-2-((1,4-dihydroxy-9,10-anthraquinone-2yl)methylene)-N-(4-fluorophenyl)hydrazinecarbothioamide (DAFPT) was synthesized, and the interaction of DAFPT with calf thymus DNA (ctDNA) was explored using ethidium bromide (EB) as a fluorescence probe. The binding mode between DAFPT and ctDNA was investigated by UV absorption spectroscopy, fluorescence spectroscopy and molecular docking. The fluorescence quenching mechanism of EB-ctDNA by DAFPT might be a combined quenching type. Thermodynamic parameters showed that the reaction was spontaneous. According to ionic strength, fluorescence polarization and melting temperature (Tm) curve results, DAFPT-ctDNA interaction was groove binding. The molecular modeling results indicated that DAFPT could slide into the A-T rich region of ctDNA. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:288 / 294
页数:7
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