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首页> 外文期刊>Chemical and Pharmaceutical Bulletin >DNA topology on an increase in positive writhing number of DNA: conformation changes in the time course of cis-diamminedichloroplatinum(II)-DNA adducts.
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DNA topology on an increase in positive writhing number of DNA: conformation changes in the time course of cis-diamminedichloroplatinum(II)-DNA adducts.

机译:DNA正向旋转数增加时的DNA拓扑结构:顺二氨二氯二氯铂(II)-DNA加合物的时间构象变化。

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We show that the topological significance of the gel mobility of cis-diamminedichloroplatinum(II) (DDP)-closed circular DNA (ccDNA) adducts decreases with reaction time, until a point at which it joins relaxed DNA, and that the mobility of the adducts increases again. There is no relationship between the relative length of the adducts and the gel mobility. Although the significance of the decrease of gel mobility is due to the unwinding of cis-DDP-DNA (or trans-DDP-DNA) adducts, the conformational significance of the subsequent increase in mobility is unclear. To elucidate the conformational significance for unwinding of the adducts, we measured the writhing number (Wk) of the adducts using electron microscopy and analyzed the topological states of cis-DDP (or trans-DDP) adducts based on the White rule, Lk=Wk+Tk. Where, Lk and Tk represent the linking and twisting number in the ring, respectively. From the data, we found that the Wk of cis-DDP-ccDNA adducts in comparison with trans-DDP-ccDNA adducts increases from a negative to a positive number with time. This suggests that cis-DDP plays a role in the change of the topological state of ccDNA. In the abstraction of platinum from the adducts with CN- ion, the differences in both topological states may explain why Pt in trans-DDP is abstracted more easily than in cis-DDP. To explain the abstraction of Pt ion, we also discuss the findings based on the thermodynamic cycle in a intermolecular crosslink model Pt(NH3)2(guanine)2(2+)-->Pt(CN)4(2-) using the Pt parametrized PM3 method.
机译:我们显示,顺式-二甲基二氯铂(II)(DDP)封闭的环状DNA(ccDNA)加合物的凝胶迁移率的拓扑意义随着反应时间的延长而降低,直到它加入松弛DNA为止,并且该加合物的迁移率再次增加。加合物的相对长度和凝胶迁移率之间没有关系。尽管降低凝胶迁移率的重要性是由于顺式-DDP-DNA(或反式-DDP-DNA)加合物的展开,但随后迁移率增加的构象意义尚不清楚。为了阐明加合物展开的构象意义,我们使用电子显微镜测量了加合物的扭转数(Wk),并基于怀特法则(Lk = Wk)分析了顺式-DDP(或反式-DDP)加合物的拓扑状态。 + Tk。其中,Lk和Tk分别表示环中的链接数和捻数。从数据中,我们发现顺式-DDP-ccDNA加合物与反式-DDP-ccDNA加合物的Wk随时间从负数增加到正数。这表明顺式-DDP在ccDNA的拓扑状态变化中起作用。从带有CN-离子的加合物中提取铂时,两种拓扑状态的差异可以解释为什么反式DDP中的Pt比顺式DDP中的Pt更容易被提取。为了解释Pt离子的抽象,我们还讨论了基于分子间交联模型Pt(NH3)2(鸟嘌呤)2(2 +)-> Pt(CN)4(2-)的热力学循环的发现。 Pt参数化PM3方法。

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