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一种d(GpG) - 铂化的十聚体双链体呈扭结状。一项扩展的核磁共振和分子力学研究。

A d(GpG)-platinated decanucleotide duplex is kinked. An extended NMR and molecular mechanics study.

作者信息

Herman F, Kozelka J, Stoven V, Guittet E, Girault J P, Huynh-Dinh T, Igolen J, Lallemand J Y, Chottard J C

机构信息

Laboratoire de Chimie et Biochimie Pharmacologiques et Toxicologiques, Université René Descartes, Paris, France.

出版信息

Eur J Biochem. 1990 Nov 26;194(1):119-33. doi: 10.1111/j.1432-1033.1990.tb19435.x.

Abstract

A conformational study of the double-stranded decanucleotide d(GCCGGATCGC).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 CGG.CCG trinucleotide where the helix is kinked by approximately 60 degrees towards the major groove and unwound by 12-19 degrees. 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 less than or equal to 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 GpG phosphate is given.

摘要

对双链十聚核苷酸d(GCCGGATCGC).d(GCGATCCGGC)进行了构象研究,其中G鸟嘌呤螯合一个顺式Pt(NH3)2部分,采用了1H和31P NMR以及分子力学方法。NMR数据与分子模型的相关性揭示了几种扭结构象之间的平衡,并排除了无扭结结构。变形集中在CGG*.CCG三核苷酸处,此处螺旋向大沟方向扭结约60度,解旋12 - 19度。模型显示与5'-G互补的胞嘧啶具有意想不到的流动性。该胞嘧啶可以堆积在扭结互补链的任何一个分支上。已计算出两个位置之间的能垒小于或等于12 kJ/mol。NMR数据支持该胞嘧啶的快速翻转。给出了在GpG*磷酸的31P共振中观察到的强烈向低场位移的解释。

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