DNA photocleavage activity of cobalt(III) polypyridyl complexes containing dpq ligand

被引:9
作者
Sun, Yi [1 ,2 ]
Zhou, Qian-Xiong [1 ]
Chen, Jing-Rong [1 ]
Hou, Yuan-Jun [1 ]
Lei, Wan-Hua [1 ]
Wang, Xue-Song [1 ]
Zhang, Bao-Wen [1 ]
机构
[1] Chinese Acad Sci, Key Lab Photochem Convers & Optoelect Mat, Tech Inst Phys & Chem, Beijing 100190, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100049, Peoples R China
关键词
Cobalt(III) complexes; dpq ligand; DNA binding; DNA photocleavage; SINGLET OXYGEN; RED-LIGHT; CLEAVAGE ACTIVITY; BINDING; DIPYRIDOPHENAZINE; RUTHENIUM(II); DERIVATIVES; NICKEL(II); GENERATION; H-1-NMR;
D O I
10.1016/j.jinorgbio.2009.09.008
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
Four cobalt(III) polypyridyl complexes, [Co(phen)(3-n)(dpq)(n)](3+) (phen = 1,10-phenanthroline, dpq = dipyrido[3,2-f:2',3'-h]-quinoxaline) (n = 0, 1, 2, and 3) were synthesized and the influences of the dpq ligand on the photophysical properties, electrochemical properties, DNA binding affinities, as well as photonuclease activities of the complexes, were examined in detail. The presence of dpq ligand increases the DNA binding affinities of the corresponding complexes remarkably with respect to [Co(phen)(3)](3+). With the sequential substitution of phen ligand by dpq ligand, the O-1(2) quantum yields of the corresponding complexes are enhanced greatly. As a result, the photonuclease activities follow the order of [Co(phen)(3)](3+) > [Co(phen)(dpq)(2)](3+) > [Co(phen)(2)(dpq)](3+) >> [Co(phen)(3)](3+). It was found all the examined complexes can generate (OH)-O-center dot upon UV irradiation, and (OH)-O-center dot is also involved in DNA photocleavage as reactive oxygen species. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:1658 / 1665
页数:8
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