期刊
METALLOMICS
卷 5, 期 3, 页码 222-231出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c3mt20214c
关键词
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资金
- National Natural Science Foundation of China [20871056, 21171070]
- Planned Item of Science and Technology of Guangdong Province [c1011220800060, c1211220800571]
- Natural Science Foundation of Guangdong Province
- Fundamental Research Funds for the Central Universities
Two ruthenium(II) polypyridyl complexes [Ru(phen)(2)(4idip)](ClO4)(2) (1) and [Ru(bpy)(2)(4idip)](ClO4)(2) (2) (phen = 1,10-phenanthroline, bpy = 2,2'-bipyridine, 4idip = 4-indoleimidazo[4,5-f][1,10]phenanthroline) designed as telomeric G-quadruplex ligands have been synthesized and characterized. The interaction of human telomeric G-quadruplex DNA (HTG21) with the designed ligands was explored by fluorescence analysis, absorption spectroscopy, continuous variation, circular dichroism spectroscopy, fluorescence resonance energy transfer (FRET) melting assay, polymerase chain reaction (PCR) stop assay, telomerase repeat amplification protocol (TRAP), and visual studies. The results showed that both complexes could induce and stabilize different G-quadruplex structures by using a 1 : 1 [quadruplex]/[complex] binding mode ratio. Complex 1 exhibited higher interaction ability and better G-quadruplex selectivity than duplex DNA. Furthermore, both ruthenium complexes led to the inhibition of the enzyme telomerase, and complex 1 was the significantly better inhibitor.
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