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通过虚拟筛选鉴定针对聚合酶 PB2 帽结合结构域的流感聚合酶抑制剂。

Identification of influenza polymerase inhibitors targeting polymerase PB2 cap-binding domain through virtual screening.

机构信息

Centre for Protein Science and Crystallography, School of Life Sciences, The Chinese University of Hong Kong, Shatin, N.T., Hong Kong, China.

Research Center of Plasmonic and Near-Infrared Science, Research Institute of Tsinghua University in Shenzhen, Shenzhen, China.

出版信息

Antiviral Res. 2017 Aug;144:186-195. doi: 10.1016/j.antiviral.2017.06.009. Epub 2017 Jun 16.

Abstract

Influenza A virus is the major cause of epidemics and pandemics worldwide. In this study, virtual screening was used to identify compounds interacting with influenza A polymerase PB2 cap-binding domain (CBD). With a database of 21,351 small molecules, 28 candidate compounds were tested and one compound (225) was identified as hit compound. Compound 225 and three of its analogs (225D1, 426 and 426Br) were found to bind directly to PB2 CBD by surface plasmon resonance (SPR). The evaluation of compounds 426Br and 225 indicated that they could bind to PB2 CBD and inhibit influenza virus at low micromolar concentration. They were predicted to bind the cap binding site of the protein by molecular modeling and were confirmed by SPR assay using PB2 CBD mutants. These two compounds have novel scaffolds and could be further developed into lead compound for influenza virus inhibition.

摘要

甲型流感病毒是全球范围内引发流行和大流行的主要原因。在这项研究中,我们使用虚拟筛选的方法来鉴定与甲型流感聚合酶 PB2 帽结合域(CBD)相互作用的化合物。在一个包含 21351 个小分子的数据库中,我们测试了 28 种候选化合物,其中一种化合物(225)被鉴定为命中化合物。通过表面等离子体共振(SPR)实验,我们发现化合物 225 及其三个类似物(225D1、426 和 426Br)能够直接与 PB2 CBD 结合。对化合物 426Br 和 225 的评估表明,它们能够以低微摩尔浓度结合 PB2 CBD 并抑制流感病毒。通过分子建模预测它们能够结合该蛋白的帽结合位点,并通过 PB2 CBD 突变体的 SPR 实验得到了证实。这两种化合物具有新颖的骨架,可进一步开发为抑制流感病毒的先导化合物。

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