Suppr超能文献

一种鸟嘌呤四链体配体复合物的结构表征。

Structural characterization of a guanine-quadruplex ligand complex.

作者信息

Read M A, Neidle S

机构信息

The CRC Biomolecular Structure Unit, Chester Beatty Laboratories, The Institute of Cancer Research, Fulham Road, London SW3 6JB, UK.

出版信息

Biochemistry. 2000 Nov 7;39(44):13422-32. doi: 10.1021/bi001584k.

Abstract

The inhibition of telomerase by molecules such as disubstituted amidoanthraquinones is believed to be due to their stabilization of guanine-quadruplex complexes. The characterization is reported of a complex with the intermolecular parallel quadruplex formed from the sequence TGGGGT and a 1,4-bis-piperidino amidoanthraquinone. Crystals obtained did not give single-crystal diffraction; the fiber-like pattern has been interpreted in terms of a repeating unit with four guanine-quartets and two stacked/intercalated ligand molecules. The two categories of possible structures for the complex consistent with this interpretation have been examined by molecular dynamics simulations, with fully solvated environments and 1000 ps simulation times. The two central guanine-quartets in the intercalation model rapidly became highly distorted, whereas the two types of models with ligand stacked externally on the ends of the quadruplex remained very stable. It was concluded that the externally bound ligand complexes best represent the structure of this quadruplex complex, in agreement with earlier NMR results on related systems.

摘要

诸如二取代氨基蒽醌等分子对端粒酶的抑制作用被认为是由于它们对鸟嘌呤-四链体复合物的稳定作用。本文报道了一种由序列TGGGGT形成的分子间平行四链体与1,4-双哌啶基氨基蒽醌形成的复合物的表征。所获得的晶体未给出单晶衍射结果;纤维状图案已根据具有四个鸟嘌呤四重体和两个堆叠/插入配体分子的重复单元进行了解释。通过分子动力学模拟,在完全溶剂化的环境和1000 ps的模拟时间下,研究了与该解释一致的复合物的两类可能结构。插入模型中的两个中央鸟嘌呤四重体迅速变得高度扭曲,而配体在四链体末端外部堆叠的两种模型则保持非常稳定。得出的结论是,外部结合的配体复合物最能代表这种四链体复合物的结构,这与早期关于相关系统的核磁共振结果一致。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验