Investigation of the interactions between methylene blue and intramolecular G-quadruplexes: an explicit distinction in electrochemical behavior

被引:11
作者
Cao, Ting [1 ]
Zhang, Fang-Ting [1 ]
Cai, Liang-Yuan [1 ]
Zhou, Ying-Lin [1 ]
Buurma, Niklaas J. [2 ]
Zhang, Xin-Xiang [1 ]
机构
[1] Peking Univ, Coll Chem, BNLMS, MOE Key Lab Bioorgan Chem & Mol Engn, 202 Chengfu Rd, Beijing 100871, Peoples R China
[2] Cardiff Univ, Sch Chem, Phys Organ Chem Ctr, Main Bldg,Pk Pl, Cardiff CF10 3AT, Wales
基金
中国国家自然科学基金;
关键词
STRUCTURAL BASIS; DNA; BINDING; PROBE; VISUALIZATION; OPTIMIZATION; COMPLEXES;
D O I
10.1039/c7an00083a
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
G-quadruplex sequences exist in eukaryotic organisms and prokaryotes, and the investigation of the interactions between G-quadruplexes and small molecule ligands is important for gene therapy, biosensor fabrication, fluorescence imaging and so on. Here, we investigated the behaviour of methylene blue (MB), an electroactive molecule, in the presence of different intramolecular G-quadruplexes by an electrochemical method using a miniaturized electrochemical device based on its intrinsic electrochemical properties. Although the effects of MB on different intramolecular G-quadruplex structures are not obvious by circular dichroism spectroscopy, distinct differences in the binding affinities of MB with different intramolecular G-quadruplexes were quickly and easily observed by an electrochemical technique. At the same time, for the human telomerase G-rich sequence (HT), the diffusion current of MB changed sensitively under different ionic conditions due to the formation of different conformations of HT, which indicated that our electrochemical method has the potential to study the influence of metal ions on the conformations of the G-quadruplexes with simplicity, rapid response and low cost. From all these, a new stacking mechanism and rule were obtained, which were also validated by docking studies and isothermal titration calorimetry (ITC).
引用
收藏
页码:987 / 993
页数:7
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