Experimental studies on photocleavage of DNA by ruthenium(II) polypyridyl complexes

被引:0
作者
Xu, H [1 ]
Li, H
Liu, Y
Mo, CY
Liang, Y
Liu, JH
Zhang, QL
Ji, LN
机构
[1] Shenzhen Univ, Normal Coll, Dept Biol & Chem, Shenzhen 518060, Peoples R China
[2] Shenzhen Univ, Coll Life Sci, Shenzhen Key Lab Microbial Genet Engn, Shenzhen 518060, Peoples R China
[3] Wuhan Univ, Coll Life Sci, Key Lab Minist Educ Virol, Wuhan 430072, Peoples R China
[4] Nanjing Univ, State Key Lab Coordinat Chem, Nanjing 210093, Peoples R China
关键词
ruthenium(II) polypyridyl complex; DNA; photocleavage; chemical nuclease;
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Photoactivated cleavage of pBR 322 DNA by a series of ruthenium(II) polypyridyl complexes has been studied. The experimental results were compared with our previous observations using spectroscopic methods and viscosity measurements. The experimental results suggest that the capacity of ruthenium(II) polypyridyl complex to photocleavage DNA depends on not only the mode and strength of the complex binding to DNA, but also the electron structure of the complex, and that ruthenium(II) polypyridyl complex can photocleavage DNA enantioselectively. The mechanism of DNA cleavage of these complexes was also discussed and proposed as follows: the excited state of Ru(II) polypyridyl. complex transfers its energy to the oxygen in solution, producing singlet molecular oxygen as the active oxygen species in the scission reactions, which oxidizes guanine of DNA and leads to cleavage of DNA. These studies are very important to the design of chemical nucleases and DNA-targeting drugs.
引用
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页码:497 / 502
页数:6
相关论文
共 30 条
[1]   METALS AND DNA - MOLECULAR LEFT-HANDED COMPLEMENTS [J].
BARTON, JK .
SCIENCE, 1986, 233 (4765) :727-734
[2]   NICKEL(III)-PROMOTED DNA CLEAVAGE WITH AMBIENT DIOXYGEN [J].
CHENG, CC ;
ROKITA, SE ;
BURROWS, CJ .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1993, 32 (02) :277-278
[3]   Picosecond time-resolved resonance Raman probing of the light-switch states of [Ru(Phen)2dppz]2+ [J].
Coates, CG ;
Olofsson, J ;
Coletti, M ;
McGarvey, JJ ;
Önfelt, B ;
Lincoln, P ;
Norden, B ;
Tuite, E ;
Matousek, P ;
Parker, AW .
JOURNAL OF PHYSICAL CHEMISTRY B, 2001, 105 (50) :12653-12664
[4]   Synthesis, characterization, DNA-binding and cleavage studies of [Ru(bpy)2(actatp)]2+ and [Ru(phen)2(actatp)]2+ (actatp=acenaphthereno[1,2-b]-1,4,8,9-tetraazariphenylence) [J].
Deng, H ;
Xu, H ;
Yang, Y ;
Li, H ;
Zou, H ;
Qu, LH ;
Ji, LN .
JOURNAL OF INORGANIC BIOCHEMISTRY, 2003, 97 (02) :207-214
[5]  
Deng H, 2002, ACTA CHIM SINICA, V60, P2159
[6]   Ternary copper complexes for photocleavage of DNA by red light: Direct evidence for sulfur-to-copper charge transfer and D-D band involvement [J].
Dhar, S ;
Senapati, D ;
Das, PK ;
Chattopadhyay, P ;
Nethaji, M ;
Chakravarty, AR .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (40) :12118-12124
[7]   Structural studies of Lambda- and Delta-[Ru(phen)(2)dppz](2+) bound to d(GTCGAC)(2): Characterization of enantioselective intercalation [J].
Dupureur, CM ;
Barton, JK .
INORGANIC CHEMISTRY, 1997, 36 (01) :33-43
[8]   Interactions of tris(phenanthroline)ruthenium(II) enantiomers with DNA:: Effects on helix flexibility studied by the electrophoretic behavior of reptating DNA in agarose gel [J].
Gisselfält, K ;
Lincoln, P ;
Nordén, B ;
Jonsson, M .
JOURNAL OF PHYSICAL CHEMISTRY B, 2000, 104 (15) :3651-3659
[9]   A H-1 NMR study of the binding of Delta-[Ru(phen)(2)DPQ](2+) to the hexanucleotide d(GTCGAC)(2). Evidence for intercalation from the minor groove [J].
Greguric, I ;
AldrichWright, JR ;
Collins, JG .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1997, 119 (15) :3621-3622
[10]   Singlet oxygen-mediated DNA photocleavage with Ru(II) polypyridyl complexes [J].
Hergueta-Bravo, A ;
Jiménez-Hernández, ME ;
Montero, F ;
Oliveros, E ;
Orellana, G .
JOURNAL OF PHYSICAL CHEMISTRY B, 2002, 106 (15) :4010-4017