Suppr超能文献

基于融合网格的CYP2C19模板系统的构建及其应用。

Construction of a fused grid-based CYP2C19-Template system and the application.

作者信息

Yamamura Yoshiya, Yoshinari Kouichi, Yamazoe Yasushi

机构信息

Laboratory of Molecular Toxicology, School of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Suruga-ku, Shizuoka, 422-8526, Japan; Non-Clinical Regulatory Science, Applied Research & Operations, Astellas Pharma Inc., 21, Miyukigaoka, Tsukuba, Ibaraki, 305-8585, Japan.

Laboratory of Molecular Toxicology, School of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Suruga-ku, Shizuoka, 422-8526, Japan.

出版信息

Drug Metab Pharmacokinet. 2023 Feb;48:100481. doi: 10.1016/j.dmpk.2022.100481. Epub 2022 Nov 9.

Abstract

A ligand-accessible space in the CYP2C19 active site was reconstituted as a fused grid-based Template with the use of structural data of the ligands. An evaluation system of CYP2C19-mediated metabolism has been developed on Template with the introduction of the idea of Trigger-residue initiated ligand-movement and fastening. Reciprocal comparison of the data of simulation on Template with experimental results suggested a unified way of the interaction of CYP2C19 and its ligands through the simultaneous plural-contact with Rear-wall of Template. CYP2C19 was expected to have a room for ligands between vertically standing parallel walls termed Facial-wall and Rear-wall, which were separated by a distance corresponding to 1.5-Ring (grid) diameter size. The ligand sittings were stabilized through contacts with Facial-wall and the left-side borders of Template including specific Position 29 or Left-end after Trigger-residue initiated ligand-movement. Trigger-residue movement is suggested to force ligands to stay firmly in the active site and then to initiate CYP2C19 reactions. Simulation experiments for over 450 reactions of CYP2C19 ligands supported the system established.

摘要

利用配体的结构数据,将CYP2C19活性位点中的一个配体可及空间重构为一个基于融合网格的模板。通过引入触发残基引发配体移动和固定的概念,在该模板上开发了一种CYP2C19介导代谢的评估系统。模板上的模拟数据与实验结果的相互比较表明,CYP2C19与其配体通过与模板后壁的同时多重接触存在一种统一的相互作用方式。预计CYP2C19在称为面壁和后壁的垂直平行壁之间有一个配体空间,这两个壁之间的距离对应于1.5环(网格)直径大小。在触发残基引发配体移动后,配体通过与面壁和模板左侧边界(包括特定位置29或左端)的接触而稳定。触发残基的移动被认为会迫使配体牢固地留在活性位点,然后引发CYP2C19反应。对CYP2C19配体的450多个反应进行的模拟实验支持了所建立的系统。

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