首页> 外文期刊>Journal of Inorganic Biochemistry: An Interdisciplinary Journal >Non-intercalative binding mode of bridged binuclear chiral Ru(II) complexes to native duplex DNA
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Non-intercalative binding mode of bridged binuclear chiral Ru(II) complexes to native duplex DNA

机译:桥接双核手性Ru(II)配合物与天然双链DNA的非插入结合模式

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A pair of chiral binuclear ruthenium(II) complexes were prepared and their binding affinities towards double stranded native DNA were assessed by observing isotropic absorption, polarized light spectra - circular and linear dichroism (CD and LD), fluorescence quenching and DNA thermal denaturation. Upon binding to DNA, the complexes produced LD signals consisting of positive and negative signals in the absorption region, although they exhibited red shift and hypochromism in the absorption spectrum. These contrasting observations indicated that the binding modes of the complexes are largely deviated from classical intercalative binding. Groove binding of the complexes to DNA was found to be more likely than intercalative binding. The small increase of DNA melting temperature in the presence of the complexes indicated a predominance of DNA groove binding. The absence of "molecular light switch effect" further supported non-intercalative binding. The groove binding propensity of complexes was also supported by comparison of the resulting data with the [Ru(phen) _2(dppz)] ~(2+).
机译:制备了一对手性双核钌(II)配合物,并通过观察各向同性吸收,偏振光谱-圆和线性二色性(CD和LD),荧光猝灭和DNA热变性来评估它们对双链天然DNA的结合亲和力。与DNA结合后,尽管它们在吸收光谱中表现出红移和色差现象,但它们在吸收区产生的LD信号由正信号和负信号组成。这些相反的观察结果表明,复合物的结合模式与经典的插层结合大相径庭。发现复合物与DNA的凹槽结合比插入结合更有可能。在存在复合物的情况下,DNA解链温度的小幅升高表明DNA凹槽结合占主导地位。缺少“分子光开关效应”进一步支持了非插入结合。通过将所得数据与[Ru(phen)_2(dppz)]〜(2+)进行比较,也支持了配合物的沟槽结合倾向。

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