Ghosh Sushobhan, Mendoza Oscar, Cubo Leticia, Rosu Frédéric, Gabelica Valérie, White Andrew J P, Vilar Ramon
Department of Chemistry, Imperial College London, London SW7 2AZ (UK).
Chemistry. 2014 Apr 14;20(16):4772-9. doi: 10.1002/chem.201304905. Epub 2014 Mar 5.
Two novel [2+2] metallo-assemblies based on a guanosine-substituted terpyridine ligand (1) coordinated to palladium(II) (2 a) and platinum(II) (2 b) are reported. These supramolecular assemblies have been fully characterized by NMR spectroscopy, ESI mass spectrometry and elemental analyses. The palladium(II) complex (2 a) has also been characterized by single crystal X-ray diffraction studies confirming that the system is a [2+2] metallo-rectangle in the solid state. The stabilities of these [2+2] assemblies in solution have been confirmed by DOSY studies as well as by variable temperature (1)H NMR spectroscopy. The ability of these dinuclear complexes to interact with quadruplex and duplex DNA was investigated by fluorescent intercalator displacement (FID) assays, fluorescence resonance energy transfer (FRET) melting studies, and electrospray mass spectrometry (ESI-MS). These studies have shown that both these assemblies interact selectively with quadruplex DNA (human telomeric DNA and the G-rich promoter region of c-myc oncogene) over duplex DNA, and are able to induce dimerization of parallel G-quadruplex structures.
报道了两种基于与钯(II)(2 a)和铂(II)(2 b)配位的鸟苷取代三联吡啶配体(1)的新型[2+2]金属配合物。这些超分子组装体已通过核磁共振光谱、电喷雾质谱和元素分析进行了全面表征。钯(II)配合物(2 a)也通过单晶X射线衍射研究进行了表征,证实该体系在固态下是一个[2+2]金属矩形。这些[2+2]组装体在溶液中的稳定性已通过扩散排序谱研究以及变温(1)H核磁共振光谱得到证实。通过荧光嵌入剂置换(FID)分析、荧光共振能量转移(FRET)熔解研究和电喷雾质谱(ESI-MS)研究了这些双核配合物与四重链和双链DNA相互作用的能力。这些研究表明,这两种组装体都能选择性地与四重链DNA(人类端粒DNA和c-myc癌基因富含G的启动子区域)而非双链DNA相互作用,并且能够诱导平行G-四重链结构的二聚化。