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9-双(吡啶-2-基甲基)氨基苯并[B]喹啉鎓的 Cu(II)配合物对 DNA 的切割。

DNA cleavage by the Cu(II) complex of the DNA-intercalating 9-bis(pyridin-2-ylmethyl)aminobenzo[b]quinolizinium.

机构信息

University of Siegen, Organic Chemistry II, Adolf-Reichwein-Str. 2, D-57068, Siegen, Germany.

出版信息

Dalton Trans. 2010 Sep 21;39(35):8195-202. doi: 10.1039/c0dt00238k. Epub 2010 Aug 4.

Abstract

The synthesis and the investigation of the Cu(II)-binding, the DNA-binding, and the DNA-damaging properties of a conjugate between the benzo[b]quinolizinium ion and the bis(pyridin-2-ylmethyl)amino receptor are presented. Photometric and fluorimetric titrations as well as CD spectroscopic analysis reveal that the 9-bis(pyridin-2-ylmethyl)aminobenzo[b]quinolizinium ligand intercalates into DNA (K(b) = 1.9 x 10(4) M(-1)) and exhibits a high selectivity towards complexation of Cu(2+) in water (K(b) = 4.3 x 10(4) M(-1)). This combination of functionalities allows to localize Cu(2+) in close proximity of DNA, where these metal ions induce efficient DNA damage, as shown by the single-strand cleavage of supercoiled plasmid DNA. Notably, the DNA cleavage does not require additional reagents nor light.

摘要

呈现了苯并[b]喹啉鎓离子与双(吡啶-2-基甲基)氨基受体之间的轭合物的 Cu(II)结合、DNA 结合和 DNA 损伤性质的合成与研究。光度和荧光滴定以及 CD 光谱分析表明,9-双(吡啶-2-基甲基)氨基苯并[b]喹啉鎓配体嵌入 DNA 中(K(b) = 1.9 x 10(4) M(-1)),并在水中对 Cu(2+)的络合表现出很高的选择性(K(b) = 4.3 x 10(4) M(-1))。这种功能的组合允许将 Cu(2+)定位在 DNA 的近距离,其中这些金属离子在不需要额外试剂和光的情况下诱导有效的 DNA 损伤,这可通过超螺旋质粒 DNA 的单链断裂来证明。值得注意的是,DNA 切割不需要额外的试剂或光。

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