Xu Li, Chen Xiang, Wu Jingheng, Wang Jinquan, Ji Liangnian, Chao Hui
MOE Key Laboratory of Bioinorganic and Synthetic Chemistry, School of Chemistry and Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275 (P.R. China); School of Chemistry and Chemical Engineering, Guangdong Pharmaceutical University, Zhongshan, 528458 (China).
Chemistry. 2015 Mar 2;21(10):4008-20. doi: 10.1002/chem.201405991. Epub 2015 Jan 23.
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 π-π 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.
合成了一系列双核钌(II)配合物,这些配合物被确定为与端粒G-四链体DNA结合的新型高选择性化合物。通过圆二色性(CD)光谱、荧光共振能量转移(FRET)熔解分析、等温滴定量热法(ITC)和分子模拟研究了这些配合物与端粒G-四链体DNA的相互作用。结果表明,配合物1、2和4在无盐或存在含100 mM K⁺缓冲液的情况下诱导并稳定了端粒DNA反平行G-四链体的形成。此外,配合物1和2与端粒G-四链体结构强烈结合并有效稳定,对G-四链体比对双链DNA具有显著的选择性。相比之下,配合物3对G-四链体的影响要小得多,这表明拥有一个大小合适的平面以与G-四联体进行良好的π-π堆积对于双核钌(II)配合物与G-四链体的相互作用至关重要。此外,研究了这四种配合物对端粒酶的抑制作用及其细胞效应,确定配合物1是端粒酶和HeLa细胞增殖最有前景的抑制剂。