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LigBuilder V3:一种多靶点药物设计方法。

LigBuilder V3: A Multi-Target Drug Design Approach.

作者信息

Yuan Yaxia, Pei Jianfeng, Lai Luhua

机构信息

Beijing National Laboratory for Molecular Sciences, State Key Laboratory for Structural Chemistry of Unstable and Stable Species, College of Chemistry and Molecular Engineering, Peking University, Beijing, China.

Center for Quantitative Biology, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing, China.

出版信息

Front Chem. 2020 Feb 28;8:142. doi: 10.3389/fchem.2020.00142. eCollection 2020.

Abstract

With the rapid development of systems-based pharmacology and poly-pharmacology, method development for rational design of multi-target drugs has becoming urgent. In this paper, we present the first multi-target drug design program LigBuilder V3, which can be used to design ligands to target multiple receptors, multiple binding sites of one receptor, or various conformations of one receptor. LigBuilder V3 is generally applicable in multi-target drug design and optimization, especially for the design of concise ligands for protein targets with large difference in binding sites. To demonstrate the utility of LigBuilder V3, we have used it to design dual-functional inhibitors targeting HIV protease and HIV reverse transcriptase with three different strategy, including multi-target design, multi-target growing, and multi-target linking. The designed compounds were computational validated by MM/GBSA binding free energy estimation as highly potential multi-target inhibitors for both HIV protease and HIV reverse transcriptase. The LigBuilder V3 program can be downloaded at "http://www.pkumdl.cn/ligbuilder3/".

摘要

随着基于系统的药理学和多药理学的快速发展,用于合理设计多靶点药物的方法开发变得迫在眉睫。在本文中,我们展示了首个多靶点药物设计程序LigBuilder V3,它可用于设计靶向多个受体、一个受体的多个结合位点或一个受体的各种构象的配体。LigBuilder V3普遍适用于多靶点药物设计和优化,尤其适用于为结合位点差异较大的蛋白质靶点设计简洁的配体。为了证明LigBuilder V3的实用性,我们使用它通过三种不同策略设计靶向HIV蛋白酶和HIV逆转录酶的双功能抑制剂,包括多靶点设计、多靶点生长和多靶点连接。通过MM/GBSA结合自由能估计对设计的化合物进行计算验证,结果表明它们是针对HIV蛋白酶和HIV逆转录酶的极具潜力的多靶点抑制剂。LigBuilder V3程序可从“http://www.pkumdl.cn/ligbuilder3/”下载。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24eb/7059350/bf9f093ffe8f/fchem-08-00142-g0001.jpg

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