计算结构生物学和人膜联蛋白A6与甲型流感病毒蛋白M2之间的相互作用模式:减少病毒感染的可能机制

Sujay Ray, A. Banerjee
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引用次数: 1

摘要

a型流感病毒是流感的主要致死致病因子。甲型流感病毒M2蛋白在病毒复制周期中起着重要作用。人类膜联蛋白A6蛋白瞄准并阻止甲型流感病毒的病毒萌芽。本文研究了膜联蛋白A6与甲型流感病毒M2蛋白在分子水平上的相互作用。执行分子建模技术,通过能量优化构建了这两种蛋白质的3D结构。通过分子对接研究分析了两种蛋白之间的相互作用。膜联蛋白A6和M2分别与Asp和Lys残基有强烈的相互作用。在与膜联蛋白A6相互作用后,M2蛋白的构象从螺旋和片状转变为螺旋状。因此,该探针有助于了解这两种蛋白的分子机制以及膜联蛋白A6对甲型流感病毒M2蛋白的负调节作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Computational structural biology and modes of interaction between human annexin A6 with influenza A virus protein M2: a possible mechanism for reducing viral infection
Influenza-A virus is a prime lethal causative factor for influenza. The M2 protein of influenza A virus plays an important responsibility in the cycle of viral replication. The human Annexin A6 protein targets and stops the viral budding for influenza A virus. Here, molecular level interactions between Annexin A6 and influenza A virus M2 protein were examined. Executing the techniques for molecular modelling, the 3D structures of the two proteins were built via energy optimisations. Interactions between the two proteins were analysed by molecular docking studies. Both Annexin A6 and M2 protein interacted strongly with a pivotal role of Asp and Lys residues, respectively. A conformational shift from helices and sheets to coils was observed in the M2 protein after its interaction with Annexin A6. This probe therefore helped to understand the molecular mechanism of the two proteins and the negative modulation of Annexin A6 on the M2 protein from influenza A virus.
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