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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Interactions of Ru(II) polypyridyl complexes with DNA mismatches and abasic sites
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Interactions of Ru(II) polypyridyl complexes with DNA mismatches and abasic sites

机译:Ru(II)聚吡啶配合物与DNA错配和无碱基位点的相互作用

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Polypyridyl based ruthenium(II) complexes, [Ru(bpy)(2)(furphen)](PF6)(2) (1) and [Ru(bpy)(2)(imiphen)](PF6)(2) (2) {furphen: 2-(furan-2-yl)-1H-imidazo[4,5-f][1,10]phenanthroline and imiphen: 2-(1H-imidazol-2-yl)-1H-imidazo[4,5-f][1,10]phenanthroline} were synthesized and characterized by ESI-MS, NMR, UV-Visible and fluorescence spectroscopic techniques. The interaction of Ru(II) complexes with calf-thymus DNA (CT DNA) as well as oligonucleotides containing mismatches and abasic sites was studied along with unmodified control DNA. Based on absorption titration studies, binding constants (K-b) for the interaction of complexes 1 and 2 with DNA were found to be 6.7 +/- 0.2 x 10(3) and 4.9 +/- 0.2 x 10(4) M-1, respectively. Hydrodynamic studies revealed weak interactions between the two complexes and CT-DNA. Luminescence studies revealed that both the complexes exhibit a five-fold increase in emission upon addition of CT-DNA. The integrated emission intensity of complexes 1 and 2 with CC mismatch oligonucleotides was 1.5 and 1.2 fold higher than that of control GC match oligonucleotides, respectively. Both the complexes did not show any specificity towards abasic or other mismatch sites except for CC mismatch. The results from this study provide an insight into the requirements of ligand shape in recognising DNA mutations such as mismatch and selectivity between DNA mismatches.
机译:聚吡啶基钌(II)络合物,[Ru(bpy)(2)(呋喃酚)] [PF6)(2)(1)和[Ru(bpy)(2)(咪芬)](PF6)(2)(2 ){呋喃酚:2-(呋喃-2-基)-1H-咪唑并[4,5-f] [1,10]菲咯啉和亚咪芬:2-(1H-咪唑-2-基)-1H-咪唑并[4合成了5-5- [1,10]菲咯啉},并通过ESI-MS,NMR,UV-Visible和荧光光谱技术对其进行了表征。研究了Ru(II)复合物与小牛胸腺DNA(CT DNA)以及含有错配和无碱基位点的寡核苷酸以及未修饰的对照DNA的相互作用。根据吸收滴定研究,发现配合物1和2与DNA相互作用的结合常数(Kb)为6.7 +/- 0.2 x 10(3)和4.9 +/- 0.2 x 10(4)M-1,分别。流体动力学研究表明两种复合物与CT-DNA之间的相互作用较弱。发光研究表明,添加CT-DNA后,两种复合物的发射量均增加了5倍。具有CC不匹配寡核苷酸的复合物1和2的积分发射强度分别比对照GC匹配寡核苷酸高1.5和1.2倍。除CC错配外,两种复合物均对无碱基或其他错配位点未显示任何特异性。这项研究的结果为认识配体形状在识别DNA突变(例如错配和DNA错配之间的选择性)方面的要求提供了见识。

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