4.6 Article

Stabilization of G-quadruplex DNA and inhibition of telomerase activity studies of ruthenium(II) complexes

期刊

JOURNAL OF INORGANIC BIOCHEMISTRY
卷 130, 期 -, 页码 122-129

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jinorgbio.2013.10.006

关键词

Ruthenium(II) complexes; G-quadruplex DNA; Telomerase; Anticancer activity

资金

  1. National Natural Science Foundation of China [20871056, 21171070, 21371075]
  2. Planned Item of Science and Technology of Guangdong Province [c1011220800060]
  3. Fundamental Research Funds for the Central Universities

向作者/读者索取更多资源

Two ruthenium(II) complexes [Ru(IP)(2)(PIP)](ClO4)(2)center dot 2H(2)O (1) and [Ru(PIP)(2)(IP)](ClO4)(2 center dot)2H(2)O (2) (IP = imidazole [4, 5-f] [1,10] phenanthroline, PIP = 2-phenylimidazo-[4, 5-f][1,10] phenanthroline) have been synthesized and characterized. The quadruplex binding of the compounds was evaluated by emission spectrum, CD spectroscopy, Visual detection assay and FRET (fluorescence resonance energy transfer)-melting assay. The results show that both complexes can induce the stabilization of quadruplex DNA, while complex 1 is a better G-quadruplex binder than complex 2. Furthermore, polymerase chain reaction-stop assay, electrophoretic mobility shift assay, telomerase repeat amplification protocol and MTT (3-[4,5-Dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide) assay demonstrate that complex 1 not only can stabilize dimer forms of the G-quadruplex at low concentrations but also exhibit better inhibitory activity for telomerase and cancer cells. (C) 2013 Elsevier Inc. All rights reserved.

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