Synthesis and copper-mediated nuclease activity of a tetracationic tris(2,2′-bipyridine) ligand

被引:11
作者
Arias, Maria-Selma [1 ]
Gonzalez-Alvarez, Marta [2 ]
Fernandez, Maria-Jose [1 ]
Lorente, Antonio [1 ]
Alzuet, Gloria [2 ]
Borras, Joaquin [2 ]
机构
[1] Univ Alcala de Henares, Dept Quim Organ, Madrid 28871, Spain
[2] Univ Valencia, Dept Quim Inorgan, E-46100 Valencia, Spain
关键词
Tetracationic tris(2,2'-bipyridine) ligand; Copper(II) complexes; DNA binding; Oxidative DNA damage; DOUBLE-STRAND DNA; COMPLEXES; CLEAVAGE; PHOTOCLEAVAGE; ACTIVATION; MECHANISMS; REACTIVITY; ACRIDINE; SCISSION; MODELS;
D O I
10.1016/j.jinorgbio.2009.05.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We report herein the synthesis of a novel tetracationic tris(2,2'-bipyridine) ligand 4. We show that this ligand metalated with copper (II), and in the presence of ascorbate as a reducing agent, strongly damages pUC18 plasmid DNA. Copper complex formation was demonstrated by ESI-MS (electrospray ionization-mass spectrum) at a 1:3 ligand to metal ratio. Binding of both 4 and its copper(II) complex to CT-DNA (calf thymus DNA) was characterized by viscosimetry, thermal denaturation and fluorescence-based competition assays. The viscosimetric data indicated that 4 and its copper(II) complex bind DNA through partial intercalation and thermal denaturation studies revealed a significant increase of duplex DNA stability in the presence of these species (Delta T-m = 16.4 and 18.3 degrees C, respectively). Moreover, 4 and its copper(II) complex were found to effectively compete with ethidium bromide for the intercalative binding sites of DNA. Overall, the copper(II)-4 complex constitutes a very efficient DNA cleaving agent in the presence of ascorbate. Experiments with scavengers further Suggest that the generation of Cu(I), hydrogen peroxide, Superoxide, hydroxyl radical and singlet oxygen-like species contributes to the DNA breakage induced by the Cu(II) complex of 4. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:1067 / 1073
页数:7
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