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受 Norharmane 铼(I)多吡啶配合物诱导的 DNA 氧化:双齿 N,N'-配体对损伤分布的影响。

DNA Oxidation Photoinduced by Norharmane Rhenium(I) Polypyridyl Complexes: Effect of the Bidentate N,N'-Ligands on the Damage Profile.

机构信息

Instituto de Investigaciones Biotecnologicas, Instituto de Tecnologia Chascomus (IIB-INTECH), Universidad Nacional de San Martin (UNSAM), I. Marino, Km 8.2, CC 164 (7130), Chascomus, Argentina.

Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas (INIFTA), Universidad Nacional de la Plata (UNLP), CCT La Plata-CONICET, Diag. 113y64, Suc. 4, C.C., 16 (B1906ZAA), La Plata, Argentina.

出版信息

Chemistry. 2018 Sep 3;24(49):12902-12911. doi: 10.1002/chem.201801272. Epub 2018 Jul 27.

DOI:10.1002/chem.201801272
PMID:29675830
Abstract

Re -polypyridyl complexes have interesting and distinctive photochemical and photosensitizing properties. This work describes the capability to induce (or photoinduce) DNA damage of three Re -complexes with a naturally occurring alkaloid called norharmane (nHo) as ligand: [Re(CO) (nHo)(L)]CF SO where L=2,2'-bipyridine (ReBpy), phenanthroline (RePhen) or dipyrido[3,2-a:2',3'-c]phenazine (ReDppz). The interaction of the complexes with DNA was investigated by steady-state and time-resolved spectroscopy. Data show that the mode and strength of interaction depend on the chemical structure of the bidentate ligand. The complexes show a major static contribution to the overall interaction, giving rise to the formation of noncovalent adducts with DNA, and the particular trend observed was RePhen>ReDppz>ReBpy. Photo-oxidation at the purine bases represents the major DNA damaging mechanism. RePhen also induces single-strand breaks in a yield similar to that of base damage, suggesting an additional photosensitizing pathway. We also performed the Ames test to evaluate the cytotoxic and mutagenic properties of both non-irradiated and photoexcited complexes. RePhen, but not the other complexes, turned out to be both toxic and phototoxic for the bacteria.

摘要

重氮吡啶配合物具有有趣且独特的光化学和光敏性质。这项工作描述了三种以天然生物碱 norharmane(nHo)为配体的 Re 配合物诱导(或光诱导)DNA 损伤的能力:[Re(CO)(nHo)(L)]CF SO,其中 L=2,2'-联吡啶(ReBpy)、菲咯啉(RePhen)或二吡啶并[3,2-a:2',3'-c]吩嗪(ReDppz)。通过稳态和时间分辨光谱研究了配合物与 DNA 的相互作用。数据表明,相互作用的方式和强度取决于双齿配体的化学结构。这些配合物对整体相互作用具有主要的静态贡献,导致与 DNA 形成非共价加合物,观察到的特定趋势为 RePhen>ReDppz>ReBpy。嘌呤碱基的光氧化代表了主要的 DNA 损伤机制。RePhen 还以类似于碱基损伤的产率诱导单链断裂,表明存在额外的光敏途径。我们还进行了 Ames 测试,以评估未辐照和光激发配合物的细胞毒性和致突变性。结果表明,RePhen 不仅对细菌有毒性,而且对光也有毒性,但其他配合物则没有。

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