Protein structure based rational design of ecdysone agonists

被引:46
作者
Holmwood, Graham [1 ]
Schindler, Michael [1 ]
机构
[1] Bayer CropSci AG, D-40789 Monheim, Germany
关键词
Ecdysteroids; Nuclear receptors; Protein X-ray structures; Insecticides; Dibenzoylhydrazide; Rational design; LIGAND-BINDING DOMAIN; QUANTITATIVE STRUCTURE; RECEPTOR; 20-HYDROXYECDYSONE; LEPIDOPTERAN; QSAR; DOCKING; ANALOGS; MODE; USP;
D O I
10.1016/j.bmc.2009.01.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
We review the impact of protein X-ray crystallography on the rational design of insecticides that act as agonists of the ligand-binding domain of the Ecdysone receptor (EcR). As the EcR is a target specific to insects, these compounds potentially constitute new chemical classes of safe insecticides. The increased insight relative to that from ligand-only based (Quantitative) Structure-Activity Relations (QSARs), classical 2D-Hansch type or 3D-CoMFA/CoMSIA (Comparative Molecular Field/Similarity Analysis), is discussed. The importance of protein X-ray structure determination in support of the discovery process is stressed as the simplistic lock-and-key picture fails due to the remarkable flexibility of the EcR ligand binding site. Several new non-steroidal chemical classes of ecdysone agonists, designed by guidance from protein X-ray studies, are described. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4064 / 4070
页数:7
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