Quadruplex DNA crystal structures and drug design

被引:132
作者
Neidle, Stephen [1 ]
Parkinson, Gary N. [1 ]
机构
[1] Univ London, Sch Pharm, Canc Res UK Biomol Struct Grp, London WC1N 1AX, England
关键词
quadruplex; crystallography; drugs;
D O I
10.1016/j.biochi.2008.03.003
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
Crystallographic studies of G-quadruplex nucleic acids have resulted in a small group of structures to date. Their morphological and detailed conformational features are described here, emphasizing the stability of the G-tetrad core and the flexibility of loops, especially upon ligand binding. Implications for drug design are discussed, in the context of the druggability of both telomeric and non-telomeric quadruplex DNAs. (C) 2008 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:1184 / 1196
页数:13
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