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Structural feature of calf thymus deoxyribonucleic acid-ruthenium(III) interaction in aqueous solution by difference Fourier transformed infrared spectroscopy

机译:差异傅里叶转化红外光谱差异傅里叶转化红外光谱法在水溶液中相互作用的CALF胸腺脱氧核糖核核酸 - 钌(III)的结构特征

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Here is the report on the interaction of ruthenium(III) species with DNA in aqueous solution at pH 7.42 by Fourier transformed infrared difference spectroscopy. Under the physiological pH and molar ratio [Ruthenium]/[DNA]=1/80-1/20 direct binding to guanine-N7, adenine-N7, and surprising binding to exocyclic thymine-O2 was found. At low metal concentration no significant shift of the absorption bands was observed, only nonspecific electrostatic binding of ruthenium(III) with negatively charged phosphate groups occurred. The increase of ruthenium(III) concentration caused DNA double helix destabilization and direct binding of the metal cation to guanine-N7 and thymine-O2. At higher ruthenium(III) concentrations denaturation of the DNA helix is evident with no apparent binding of ruthenium(III) to adenine and cytosine. Helix opening allows migration of ruthenium(III) ions from phosphate to available nucleobases (guanine and thymine). No alteration of the sugar phosphate geometry was observed thus confirming that DNA remains in B conformation.
机译:以下是通过傅里叶转化的红外差异光谱分析pH7.42在pH7.42的水溶液中具有DNA的钌(III)物种与DNA相互作用的报告。在生理pH和摩尔比[钌] / [DNA] = 1 / 80-1 / 20直接与鸟嘌呤-N7,腺嘌呤-N7和与官方胸腺嘧啶-O2令人惊讶的结合。在低金属浓度下,观察到吸收带的显着偏移,仅发生带负电荷的磷酸盐基团的钌(III)的非特异性静电结合。钌(III)浓度的增加导致DNA双螺旋稳定性和金属阳离子直接结合到鸟嘌呤-N7和胸腺嘧啶-O2。在较高的钌(III)浓度下,DNA螺旋的变性是明显的,无明显结合钌(III)至腺嘌呤和胞嘧啶。螺旋开口允许将钌(III)离子从磷酸盐迁移到可用的核碱基(鸟嘌呤和胸腺嘧啶)。因此,不观察到糖磷酸盐几何形状的改变,因此证实DNA保持在B构象中。

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