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Ro15 - 1788的分子结构以及苯二氮䓬受体配体结合模型。拮抗剂共同特征的结构鉴定。

Molecular structure of Ro15-1788 and a model for the binding of benzodiazepine receptor ligands. Structural identification of common features in antagonists.

作者信息

Codding P W, Muir A K

出版信息

Mol Pharmacol. 1985 Aug;28(2):178-84.

PMID:2991738
Abstract

Ligands that bind to the benzodiazepine receptor have three possible effects. The ligand can be an agonist and reduce anxiety, an antagonist and have no biological effect, or an inverse agonist and promote convulsions. This receptor complex is unique in its spectrum of response to ligands, and conformational changes in the receptor are implicated. The x-ray crystal structure of an imidazobenzodiazepine antagonist ligand, Ro15-1788, was determined and compared to the structures of the 1,4-benzodiazepine agonists and to two other types of antagonists, beta-carbolines and a pyrazoloquinolinone, CGS-8216. The antagonists were found to have similar arrangements of binding features including an aromatic ring, a carbonyl oxygen atom, and a hydrophobic side chain. The structures of these antagonists could be superimposed in a model binding site with three common features for all of the antagonists and a fourth hydrogen-bonding site for the pure antagonists (or inverse agonists), the beta-carbolines, and CGS-8216. A comparison of the shapes of the antagonist benzodiazepine, Ro15-1788, and several agonists showed that RO15-1788 has a unique azepine ring conformation that distorts the usual arrangement of the aromatic A ring, carbonyl oxygen atom, and imine N atom of the agonists. A conformational adjustment in the receptor would be required to accommodate both of these types of ligands. A summary of the superpositions of typical agonists and the antagonists leads to a model with 7 conformationally mobile binding points. Inverse agonists are distinguished from antagonists by the length of the hydrophobic side chain. Antagonists are distinguished from agonists in part by the lack of a binding feature similar to the imine N atom of the diazepine ring. This model accounts for the key features found in ligands for the benzodiazepine receptor and provides an explanation for the spectrum of responses elicited by receptor binding.

摘要

与苯二氮䓬受体结合的配体有三种可能的效应。该配体可以是激动剂,能减轻焦虑;可以是拮抗剂,无生物学效应;或者是反向激动剂,会引发惊厥。这种受体复合物对配体的反应谱很独特,且受体的构象变化与之相关。确定了一种咪唑并苯二氮䓬拮抗剂配体Ro15 - 1788的X射线晶体结构,并将其与1,4 - 苯二氮䓬激动剂以及另外两种拮抗剂(β-咔啉和吡唑并喹啉酮CGS - 8216)的结构进行比较。发现这些拮抗剂具有相似的结合特征排列,包括一个芳香环、一个羰基氧原子和一个疏水侧链。这些拮抗剂的结构可以叠加在一个模型结合位点上,该位点对所有拮抗剂有三个共同特征,对纯拮抗剂(或反向激动剂)、β-咔啉和CGS - 8216还有第四个氢键结合位点。拮抗剂苯二氮䓬Ro15 - 1788与几种激动剂的形状比较表明,Ro15 - 1788具有独特的氮杂䓬环构象,这种构象扭曲了激动剂中芳香A环、羰基氧原子和亚胺N原子的通常排列。受体需要进行构象调整以容纳这两种类型的配体。典型激动剂和拮抗剂叠加的总结得出一个具有7个构象可变结合点的模型。反向激动剂与拮抗剂的区别在于疏水侧链的长度。拮抗剂与激动剂的部分区别在于缺乏与二氮䓬环亚胺N原子类似的结合特征。该模型解释了苯二氮䓬受体配体中发现的关键特征,并为受体结合引发的反应谱提供了一种解释。

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