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Antitumor Drug Mitoxantrone Do Not Preclude Salt-driven B-Z Transition of Poly (dG- dC)

机译:抗肿瘤药物米托蒽醌不排除聚(dG- dC)的盐驱动B-Z转变

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Despite of the existence in literature of large number of reports the binding modes of mitoxantrone (MTX) with DNA must be subject to refinement. Moreover there is no any report yet on interaction of MTX with Z-DNA. Here we present results of circular dichroism (CD) studies on MTX binding to salt driven left-handed conformation of poly(dG- dC). It was shown, that in contrast with classical intercalating ligands (ethidium bromide, acridine orange etc.) that bind with B-form DNA and obstacle B-Z transition at high concentrations of NaCl MTX interferes B-Z transition, but does not prevent the transitions process, thus suggest the semi intercalating (partial stacking) mode of MTX interaction with Z-form of DNA.
机译:尽管文献中存在大量报道,但米托蒽醌(MTX)与DNA的结合方式必须加以改进。而且,还没有关于MTX与Z-DNA相互作用的任何报道。在这里,我们介绍了MTX与盐驱动的poly(dG- dC)左旋构象结合的圆二色性(CD)研究结果。结果表明,与经典的插层配体(溴化乙锭,a啶橙等)形成鲜明对比的是,在高浓度的NaCl MTX中与B型DNA结合并阻碍BZ过渡,但会干扰BZ过渡,但不会阻止过渡过程,因此建议MTX与DNA的Z型相互作用的半嵌入(部分堆叠)模式。

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