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铜(II)促进博来霉素介导的质粒DNA解旋。

Copper(II) facilitates bleomycin-mediated unwinding of plasmid DNA.

作者信息

Levy M J, Hecht S M

机构信息

Department of Chemistry, University of Virginia, Charlottesville 22901.

出版信息

Biochemistry. 1988 Apr 19;27(8):2647-50. doi: 10.1021/bi00408a002.

Abstract

The unwinding of plasmid DNA by bleomycin A2 (BLM A2) was investigated by use of two-dimensional gel electrophoresis. It was found that Cu2+ ions greatly facilitated the unwinding of topoisomers of plasmid DNA by BLM A2 at concentrations where cupric ions alone had no effect on DNA supercoiling. The concentration of BLM A2 required for observable unwinding was reduced at least 100-fold in the presence of equimolar Cu2+. A plot of [Cu2+] vs extent of DNA unwinding in the presence of 10(-4) M BLM A2 gave a curve consistent with the action of cupric ions on BLM in an allosteric fashion, possibly rearranging the drug into a conformation that facilitates DNA unwinding. The participation of the metal center in enhancing DNA unwinding via direct ionic interaction with one or more negatively charged groups on the DNA duplex also seems possible. Further analysis of the structural factors required for BLM-mediated DNA unwinding was carried out with Cu2+ + BLM demethyl A2, the latter of which differs from BLM A2 only in that it lacks a methyl group, and associated positive charge, at the C-terminus. Cu(II).BLM demethyl A2 was found to be much less effective than Cu(II).BLM A2 as a DNA unwinding agent, emphasizing the strong dependence of this process on the presence of positively charged groups within the BLM molecule. These findings constitute the first direct evidence that the metal center of BLM can participate in DNA interaction, as well as in the previously recognized role of oxygen binding and activation.

摘要

运用二维凝胶电泳技术研究了博来霉素A2(BLM A2)对质粒DNA的解旋作用。研究发现,在铜离子单独存在时对DNA超螺旋无影响的浓度下,Cu2+离子极大地促进了BLM A2对质粒DNA拓扑异构体的解旋。在等摩尔Cu2+存在的情况下,可观察到解旋所需的BLM A2浓度至少降低了100倍。在存在10^(-4) M BLM A2的情况下,绘制[Cu2+]与DNA解旋程度的关系图,得到的曲线与铜离子以别构方式作用于BLM一致,可能是将药物重排为有助于DNA解旋的构象。金属中心通过与DNA双链上一个或多个带负电荷的基团直接离子相互作用来增强DNA解旋的参与也似乎是可能的。用Cu2+ + BLM去甲基A2对BLM介导的DNA解旋所需的结构因素进行了进一步分析,后者与BLM A2的不同之处仅在于其C端缺少一个甲基及相关的正电荷。发现Cu(II).BLM去甲基A2作为DNA解旋剂的效果远不如Cu(II).BLM A2,强调了这一过程对BLM分子内带正电荷基团存在的强烈依赖性。这些发现构成了首个直接证据,表明BLM的金属中心可参与DNA相互作用,以及先前已认识到的氧结合和激活作用。

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