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十二聚核苷酸双链体中链内顺式-[Pt(NH₃)₂(d(GpCpG))]加合物的结构:I. ¹H和³¹P核磁共振研究

Structure of the intrastrand cis-[Pt(NH3)2(d(GpCpG))] adduct in a dodecanucleotide duplex: I. A 1H and 31P n.m.r. study.

作者信息

Ptak M, Rahmouni A, Mazeau K, Thuong N T, Leng M

机构信息

Centre de Biophysique Moléculaire (CNRS), Université d'Orléans, France.

出版信息

Anticancer Drug Des. 1989 Jun;4(1):53-61.

PMID:2757752
Abstract

The structure of an intrastrand cis-[Pt(NH3)2(d(GpCpG))] adduct in a dodecanucleotide duplex has been investigated by using ultraviolet absorption, circular dichroism, 1H and 31P n.m.r. The binding of cis-DDP does not inhibit the formation of a duplex but it induces a lowering of congruent to 26 degrees C of its melting temperature. A broadening of the 1H spectrum prevents an accurate analysis of the platination site. Nevertheless, by considering its thermal behavior and the number of imino protons a model of structure of the platinated duplex is proposed in which the central C.G. pair is disrupted and a neighboring C.G pair is very accessible or distorted. The environment of two phosphate groups is disturbed by the cis-DDP binding.

摘要

通过紫外吸收、圆二色性、1H和31P核磁共振研究了十二核苷酸双链体中链内顺式-[Pt(NH3)2(d(GpCpG))]加合物的结构。顺铂的结合并不抑制双链体的形成,但会导致其熔解温度降低约26℃。1H谱的展宽妨碍了对铂化位点的精确分析。然而,通过考虑其热行为和亚氨基质子的数量,提出了一种铂化双链体的结构模型,其中中心C.G.对被破坏,相邻的C.G.对非常容易接近或发生扭曲。两个磷酸基团的环境因顺铂的结合而受到干扰。

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