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DNA binding studies of ruthenium(II) complexes containing asymmetric tridentate ligands
被引:230
|作者:
Chao, H
[1
]
Mei, WJ
Huang, QW
Ji, LN
机构:
[1] Zhongshan Univ, Dept Chem, Guangzhou 510275, Peoples R China
[2] Zhongshan Univ, State Key Lab Optoelect Mat & Technol, Guangzhou 510275, Peoples R China
[3] Shanghai Inst Organ Chem, State Key Lab Bioorgan & Nat Prod Chem, Shanghai 200032, Peoples R China
[4] Nanjing Univ, State Key Lab Coordinat Chem, Nanjing 210093, Peoples R China
基金:
中国国家自然科学基金;
美国国家科学基金会;
关键词:
ruthenium complexes;
polypyridine ligands;
DNA binding;
D O I:
10.1016/S0162-0134(02)00543-3
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:
Absorption spectroscopy, fluorescence spectroscopy and viscosity measurements have been used to characterize the DNA binding of [Ru(tpy)(dppt)](2+) (tpy=2,2':6',2"-terpyridine, dppt=3-(1,10-phenanthrolin-2-yl)-5,6-diphenyl-as-triazine), [Ru(tpy)(pta)](2+) (pta=3(1,10-phenanthrolin-2-yl)-as-triazino[5,6-f]acenaphthylene) and [Ru(tpy)(Ptp)](2+) (ptp=3-(1,10-phenanthrolin-2-yl)-as-triazino[5,6-f]phenanthrene). The results indicate that [Ru(tpy)(pta)](2+) and [Ru(tpy)(ptp)](2+) bindwith CT-DNA in an intercalative mode, while [Ru(tpy)(dppt)](2+) binds with DNA by partial intercalation. The ligand planarity of the complex has a significant effect on DNA binding affinity increases in the order [Ru(tpy)(dppt)](2+) <[Ru(tpy)(pta)](2+) <[Ru( tpy)(Ptp)](2+). (C) 2002 Elsevier Science Inc. All rights reserved.
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页码:165 / 170
页数:6
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