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

机译:通过虚拟筛选鉴定靶向聚合酶PB2帽结合域的流感聚合酶抑制剂

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摘要

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. (C) 2017 Elsevier B.V. All rights reserved.
机译:流感病毒是全世界流行病学和流行病的主要原因。 在该研究中,使用虚拟筛选来鉴定与流感的聚合酶PB2帽结合结构域(CBD)相互作用的化合物。 对于21,351个小分子的数据库,测试了28个候选化合物,并将一种化合物(225)鉴定为麦片化合物。 发现其化合物225和三种类似物(225d1,426和426br)通过表面等离子体共振(SPR)直接与PB2 CBD结合。 化合物426Br和225的评价表明它们可以在低微摩拉浓度下抑制流感病毒并抑制流感病毒。 预计它们通过分子建模结合蛋白质的盖子结合位点,并使用PB2 CBD突变体通过SPR测定证实。 这两种化合物具有新的支架,可以进一步开发成用于流感病毒抑制的铅化合物。 (c)2017 Elsevier B.v.保留所有权利。

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