A D(GPG)-PLATINATED DECANUCLEOTIDE DUPLEX IS KINKED - AN EXTENDED NMR AND MOLECULAR MECHANICS STUDY

被引:104
作者
HERMAN, F
KOZELKA, J
STOVEN, V
GUITTET, E
GIRAULT, JP
HUYNHDINH, T
IGOLEN, J
LALLEMAND, JY
CHOTTARD, JC
机构
[1] UNIV PARIS 05,CNRS,URA 400,CHIM & BIOCHIM PHARMACOL & TOXICOL LAB,45 RUE ST PERES,F-75270 PARIS 06,FRANCE
[2] INST PASTEUR,CNRS,URA 487,CHIM ORGAN LAB,F-75724 PARIS 15,FRANCE
[3] CNRS,INST CHIM SUBST NAT,RESONANCE MAGNET NUCL LAB,F-91190 GIF SUR YVETTE,FRANCE
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 1990年 / 194卷 / 01期
关键词
D O I
10.1111/j.1432-1033.1990.tb19435.x
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
A conformational study of the double‐stranded decanucleotide d(GCCG*G*ATCGC) · d(GCGATCCGGC), with the G* guanines chelating a cis‐Pt(NH3)2 moiety, has been accomplished using 1H and 31P NMR, and molecular mechanics. Correlation of the NMR data with molecular models has disclosed an equilibrium between several kinked conformations and has ruled out an unkinked structure. The deformation is localized at the CG*G*· CCG trinucleotide where the helix is kinked by approximately 60° towards the major groove and unwound by 12–19°. The models revealed an unexpected mobility of the cytosine complementary to the 5′‐G*. This cytosine can stack on either branch of the kinked complementary strand. The energy barrier between the two positions has been calculated to be ≤ 12 kJ/mol. The NMR data are in support of rapid flip‐flopping of this cytosine. An explanation for the strong downfield shift observed in the 31P resonance of the G*pG* phosphate is given. Copyright © 1990, Wiley Blackwell. All rights reserved
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页码:119 / 133
页数:15
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