Williams Dominique E, Fischer Christina M, Kassai Miki, Gude Lourdes, Fernández María-José, Lorente Antonio, Grant Kathryn B
Department of Chemistry, Georgia State University, P.O. Box 3965, Atlanta, GA 30302-3965, United States.
Departamento de Química Orgánica y Química Inorgánica, Universidad de Alcalá, 28871-Alcalá de Henares, Madrid, Spain.
J Inorg Biochem. 2017 Mar;168:55-66. doi: 10.1016/j.jinorgbio.2016.12.007. Epub 2016 Dec 15.
This paper describes the synthesis of a trinuclear Cu(II) complex (4) containing a central 1,4,5,8,9,12-hexaazatriphenylene-hexacarboxylate (hat) core (3). Low, micromolar concentrations of the negatively charged parent ligand 3 and the neutral trinuclear complex 4 were found to photocleave negatively charged pUC19 plasmid DNA with high efficiency at neutral pH (350nm, 50min, 22°C). The interactions of complex 4 with double-helical DNA were studied in detail. Scavenger and colorimetric assays pointed to the formation of Cu(I), superoxide anion radicals, hydrogen peroxide, and hydroxyl radicals during photocleavage reactions. UV-visible absorption, circular dichroism, DNA thermal denaturation, and fluorescence data suggested that the Cu(II) complex contacts double-stranded DNA in an external fashion. The persistent association of ligand 3 and complex 4 with Na(I) and/or other cations in aqueous solution might facilitate electrostatic DNA interactions.
本文描述了一种含有中心1,4,5,8,9,12-六氮杂三亚苯六羧酸盐(hat)核心(3)的三核铜(II)配合物(4)的合成。发现在中性pH值(350nm,50分钟,22°C)下,低至微摩尔浓度的带负电荷的母体配体3和中性三核配合物4能高效光裂解带负电荷的pUC19质粒DNA。详细研究了配合物4与双链DNA的相互作用。清除剂和比色测定表明,光裂解反应过程中会形成Cu(I)、超氧阴离子自由基、过氧化氢和羟基自由基。紫外可见吸收、圆二色性、DNA热变性和荧光数据表明,铜(II)配合物以外部方式与双链DNA接触。配体3和配合物4在水溶液中与Na(I)和/或其他阳离子的持续缔合可能有助于静电DNA相互作用。