Dinuclear Ruthenium(II) Complexes That Induce and Stabilise G-Quadruplex DNA

被引:62
|
作者
Xu, Li [1 ,2 ]
Chen, Xiang [1 ]
Wu, Jingheng [1 ]
Wang, Jinquan [1 ]
Ji, Liangnian [1 ]
Chao, Hui [1 ]
机构
[1] Sun Yat Sen Univ, Sch Chem & Chem Engn, MOE Key Lab Bioinorgan & Synthet Chem, Guangzhou 510275, Guangdong, Peoples R China
[2] Guangdong Pharmaceut Univ, Sch Chem & Chem Engn, Zhongshan 528458, Peoples R China
基金
美国国家科学基金会;
关键词
conformation analysis; DNA; G-quadruplexes; ruthenium; telomeres; TELOMERIC G-QUADRUPLEX; MOLECULAR LIGHT SWITCH; CIRCULAR-DICHROISM; DRUG-RECOGNITION; METAL-COMPLEXES; K+ SOLUTION; C-MYC; LIGANDS; BINDING; INHIBITION;
D O I
10.1002/chem.201405991
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A series of dinuclear ruthenium(II) complexes were synthesised, and the complexes were determined to be new highly selective compounds for binding to telomeric G-quadruplex DNA. The interactions of these complexes with telomeric G-quadruplex DNA were studied by using circular dichroism (CD) spectroscopy, fluorescence resonance energy transfer (FRET) melting assays, isothermal titration calorimetry (ITC) and molecular modelling. The results showed that the complexes 1, 2 and 4 induced and stabilised the formation of antiparallel G-quadruplexes of telomeric DNA in the absence of salt or in the presence of 100 mm K+-containing buffer. Furthermore, complexes 1 and 2 strongly bind to and effectively stabilise the telomeric G-quadruplex structure and have significant selectivity for G-quadruplex over duplex DNA. In comparison, complex 3 had a much lesser effect on the G-quadruplex, suggesting that possession of a suitably sized plane for good pi-pi stacking with the G-quadruplets is essential for the interaction of the dinuclear ruthenium(II) complexes with the G-quadruplex. Moreover, telomerase inhibition by the four complexes and their cellular effects were studied, and complex 1 was determined to be the most promising inhibitor of both telomerase and HeLa cell proliferation.
引用
收藏
页码:4008 / 4020
页数:13
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