SEQUENCE-DEPENDENT DISTORTIONS INDUCED IN DNA BY MONOFUNCTIONAL PLATINUM(II) BINDING

被引:141
作者
BRABEC, V [1 ]
REEDIJK, J [1 ]
LENG, M [1 ]
机构
[1] CNRS,CTR BIOPHYS MOLEC,1A AVE RECH SCI,F-45071 ORLEANS 2,FRANCE
关键词
D O I
10.1021/bi00164a014
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
The effects on thermal stability and conformation of DNA produced by the monofunctional adducts of chlorodiethylenetriamineplatinum(II) chloride {[Pt(dien)Cl]Cl} have been investigated. Oligodeoxyribonucleotide duplexes of varying lengths (9-20 base pairs) and of varying central trinucleotide sequences were prepared and characterized that contained site-specific and unique N(7)-guanine adducts. Included are adducts at the sequences of d(AGC), d(AGT), d(CGA), d(TGA), d(TGC), and d(TGT). All these monofunctional adducts decrease the melting temperature (T(m)) of the duplexes. This destabilization effect exhibits a sequence-dependent variability. The highest lowering of T(m) is observed for the modified duplexes containing the central sequence of pyrimidine-guanine-pyrimidine. The destabilization effect is reduced with decreasing concentrations of Na+. Polarography, circular dichroism, phenanthroline-copper, and chemical probes reveal conformational distortions spreading over several base pairs around the adduct. The effects of monofunctional platinum(II) adducts on conformational distortions in DNA exhibit a sequence-dependent variability similar to those on thermal stability of DNA. The influence of the monofunctional adduct formed by cis-diamminemonoaquamonochloroplatinum(II) on the stability of the oligonucleotide duplex has been also studied. This lesion decreases thermal stability of DNA in the same way as does the adduct of [Pt(dien)Cl]Cl.
引用
收藏
页码:12397 / 12402
页数:6
相关论文
共 36 条
[1]   PT-195 NMR KINETIC AND MECHANISTIC STUDIES OF CIS-DIAMMINEDICHLOROPLATINUM AND TRANS-DIAMMINEDICHLOROPLATINUM(II) BINDING TO DNA [J].
BANCROFT, DP ;
LEPRE, CA ;
LIPPARD, SJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1990, 112 (19) :6860-6871
[2]   BENDING STUDIES OF DNA SITE-SPECIFICALLY MODIFIED BY CISPLATIN, TRANS-DIAMMINEDICHLOROPLATINUM(II) AND CIS-[PT(NH3)2(N3-CYTOSINE)CL]+ [J].
BELLON, SF ;
LIPPARD, SJ .
BIOPHYSICAL CHEMISTRY, 1990, 35 (2-3) :179-188
[3]   DNA UNWINDING PRODUCED BY SITE-SPECIFIC INTRASTRAND CROSS-LINKS OF THE ANTITUMOR DRUG CIS-DIAMMINEDICHLOROPLATINUM(II) [J].
BELLON, SF ;
COLEMAN, JH ;
LIPPARD, SJ .
BIOCHEMISTRY, 1991, 30 (32) :8026-8035
[4]   BIOPHYSICAL STUDIES OF THE MODIFICATION OF DNA BY ANTITUMOR PLATINUM COORDINATION-COMPLEXES [J].
BRABEC, V ;
KLEINWACHTER, V ;
BUTOUR, JL ;
JOHNSON, NP .
BIOPHYSICAL CHEMISTRY, 1990, 35 (2-3) :129-141
[5]  
BRABEC V, 1983, COLLECT CZECH CHEM C, V48, P2903
[6]   REEVALUATION OF INTERACTION OF CIS-DICHLORO(ETHYLENEDIAMINE)PLATINUM(II) WITH DNA [J].
EASTMAN, A .
BIOCHEMISTRY, 1986, 25 (13) :3912-3915
[8]  
FICHTINGERSCHEP.AM, 1986, BIOCHEMISTRY-US, V28, P7975
[10]  
HOLLIS LS, 1991, CANCER RES, V51, P1866