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Issue 13, 2013
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Targeting telomeric G-quadruplexes with the ruthenium(II) complexes [Ru(bpy)2(ptpn)]2+ and [Ru(phen)2(ptpn)]2+

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Abstract

Two ruthenium(II) polypyridyl complexes, [Ru(bpy)2(ptpn)]2+ (1) (bpy = 2,2′-bipyridine, ptpn = 3-(1,10-phenanthroline-2-yl)-as-triazino[5,6-f]1,10-phenanthroline) and [Ru(phen)2(ptpn)]2+ (2) (phen = 1,10-phenanthroline), were synthesized and characterized. Crystal structure analysis shows that complex 1 has a large planar aromatic area and possesses the potential to fit the geometric structure of G-quadruplex. The interaction of the G-quadruplex DNA with Ru(II) complexes was explored by means of circular dichroism (CD), fluorescence resonance energy transfer (FRET) melting assay, competitive FRET assay and polymerase chain reaction (PCR) stop assay. The results indicated that complexes 1 and 2 both have the ability to promote the formation and stabilization of the human telomeric d[(TTAGGG)n] (HTG22) quadruplex and exhibit high G-quadruplex DNA selectivity over duplex DNA. The telomere repeat amplification protocol (TRAP) assay and long-term proliferation experiments further demonstrate that the Ru(II) complexes are potent telomerase inhibitors and HeLa cell proliferation inhibitors.

Graphical abstract: Targeting telomeric G-quadruplexes with the ruthenium(ii) complexes [Ru(bpy)2(ptpn)]2+ and [Ru(phen)2(ptpn)]2+

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Publication details

The article was received on 05 Dec 2012, accepted on 09 Jan 2013 and first published on 10 Jan 2013


Article type: Paper
DOI: 10.1039/C3DT32921F
Citation: Dalton Trans., 2013,42, 4386-4397
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    Targeting telomeric G-quadruplexes with the ruthenium(II) complexes [Ru(bpy)2(ptpn)]2+ and [Ru(phen)2(ptpn)]2+

    X. Chen, J. Wu, Y. Lai, R. Zhao, H. Chao and L. Ji, Dalton Trans., 2013, 42, 4386
    DOI: 10.1039/C3DT32921F

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