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钴配合物催化亚硫酸盐自氧化导致的DNA损伤

DNA damage by sulfite autoxidation catalyzed by cobalt complexes.

作者信息

Alipázaga María V, Moreno Ruben G M, Linares Edlaine, Medeiros Marisa H G, Coichev Nina

机构信息

Instituto de Química, Universidade de São Paulo, CP 26077, CEP 05513-970, São Paulo, SP, Brazil.

出版信息

Dalton Trans. 2008 Nov 7(41):5636-44. doi: 10.1039/b805222k. Epub 2008 Sep 8.

DOI:10.1039/b805222k
PMID:18854902
Abstract

DNA damage was investigated in the presence of sulfite, dissolved oxygen and cobalt(II) complexes with glycylglycylhistidine, glycylhistidyllysine, glycylglycyltyrosylarginine and tetraglycine. These studies indicated that only Co(II) complexed with glycylglycylhistidine (GGH) induced DNA strand breaks at low sulfite concentrations (1-80 microM) via strong oxidants formed in the reaction. In the presence of the other complexes, some damage occurred only in the presence of high sulfite concentrations (0.1-2.0 mM) after incubation for 4 h. In the presence of GGH, Co(II) and dissolved O2, DNA damage must involve a reactive high-valent cobalt complex. The damaging effect was increased by adding S(IV), due to the oxysulfur radicals formed as intermediates in S(IV) autoxidation catalyzed by the complex. SO3 -, HO and H radicals were detected by EPR-spin trapping experiments with DMPO (5,5-dimethyl-1-pyrroline N-oxide). The results indicate that Co(II) binds O2 in the presence of GGH, and leads to the formation of a DMPO-HO adduct without first forming free superoxide or hydroxyl radical, supporting the participation of a reactive high-valent cobalt complex.

摘要

在亚硫酸盐、溶解氧以及钴(II)与甘氨酰甘氨酰组氨酸、甘氨酰组氨酰赖氨酸、甘氨酰甘氨酰酪氨酰精氨酸和四甘氨酸形成的配合物存在的情况下,对DNA损伤进行了研究。这些研究表明,只有钴(II)与甘氨酰甘氨酰组氨酸(GGH)形成的配合物在低亚硫酸盐浓度(1 - 80 microM)下通过反应中形成的强氧化剂诱导DNA链断裂。在其他配合物存在的情况下,仅在高亚硫酸盐浓度(0.1 - 2.0 mM)下孵育4小时后才会发生一些损伤。在GGH、钴(II)和溶解氧存在的情况下,DNA损伤必定涉及一种具有反应活性的高价钴配合物。添加S(IV)会增强损伤效应,这是由于在配合物催化的S(IV)自氧化过程中形成的氧硫自由基作为中间体所致。通过使用DMPO(5,5 - 二甲基 - 1 - 吡咯啉N - 氧化物)的EPR自旋捕获实验检测到了SO3 - 、HO和H自由基。结果表明,钴(II)在GGH存在的情况下结合氧气,并导致形成DMPO - HO加合物,而无需首先形成游离的超氧化物或羟基自由基,这支持了一种具有反应活性的高价钴配合物的参与。

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