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首页> 外文期刊>Bulletin of the Korean Chemical Society >DNA Mediated Energy Transfer from 4',6-Diamidino-2-phenylindole to Ru(II)[(l,10-phenanthroline)_2L]~(2+):Effect of Ligand Structure
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DNA Mediated Energy Transfer from 4',6-Diamidino-2-phenylindole to Ru(II)[(l,10-phenanthroline)_2L]~(2+):Effect of Ligand Structure

机译:DNA介导的4',6-二6-基-2-苯基吲哚向Ru(II)[(1,10-菲咯啉)_2L]〜(2+)的能量转移:配体结构的影响

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摘要

It was proposed that Ru(II)[(l,10-phenanthroline)_2dipyrido[3,2-a:2',3'-c]phenazine([Ru(phen)_2DPPZ]~(2+))complexes and 4',6-diamidino-2-phenylindole(DAPI)simultaneously bind to poly[d(A-T)_2](Biophysics.J.2003,85,3865).Forster type resonance energy transfer from excited DAPI to [Ru(phen)_2DPPZ]~(2+)complexes was observed.In this study,we synthesized A-and A-[Ru(phenanthroline)_2dipyrido[3,2-a:2',3'-c]6-azaphenazine]([Ru(phen)_2DPAPZ]~(2+))at which the DNA intercalating ligand DPPZ was replaced and we studied its binding properties to poly[d(A-T)_2] in the presence and absence of DAPI using polarized spectroscopy and fluorescence techniques.All the spectroscopic properties of the [Ru(phen)_2DPAPZ]~(2+)-poly[d(A-T)_2] complex were the same in the presence and absence of DAPI that blocks the minor groove of polynucleotide,suggesting both A-and A-[Ru(phen)_2DPAPZ]~(2+)complexes are located at the major groove of poly[d(A-T)_2].On the other hand,in contrast with [Ru(phen)_2DPPZ]~(2+),both A-and A-[Ru(phen)_2DPAPZ]~(2+)exhibited almost twice the efficiency in the fluorescence quenching of DAPI that binds at the minor groove of poly[d(A-T)_2].This observation indicates that the efficiency of the Forster type resonance energy transfer can be controlled by a small change in the chemical structure of the intercalated ligand.
机译:有人提出Ru(II)[(1,10-菲咯啉)_2双吡啶[3,2-a:2',3'-c]吩嗪([Ru(phen)_2DPPZ]〜(2+))络合物和4 ',6-二mid基-2-苯基吲哚(DAPI)同时与聚[d(AT)_2]结合(生物物理学.J.2003,85,3865)。Forster型共振能量从激发的DAPI转移到[Ru(phen)_2DPPZ观察到]〜(2+)络合物。在这项研究中,我们合成了A-和A- [Ru(菲咯啉)_2双吡啶[3,2-a:2',3'-c] 6-氮杂吩嗪]([Ru( phen)_2DPAPZ]〜(2+))取代了DNA嵌入配体DPPZ,并使用偏振光谱和荧光技术研究了在有无DAPI的情况下其与聚[d(AT)_2]的结合特性。 [Ru(phen)_2DPAPZ]〜(2 +)-poly [d(AT)_2]络合物的光谱性质在存在和不存在阻断多核苷酸小沟的DAPI的情况下是相同的,建议A和A -[Ru(phen)_2DPAPZ]〜(2+)配合物位于聚[d(AT)_2]的主沟处。另一方面,与[Ru(phen)_2DPPZ]〜(2+)形成对比,两者A-和A- [Ru(phen)_2DPAPZ]〜(2+)的荧光猝灭效率几乎是在聚[d(AT)_2]的小沟处结合的DAPI的两倍。这一观察表明,该效率插入式配体的化学结构的微小变化可以控制Forster型共振能量的传递。

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