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首页> 外文期刊>Proteomics >Interactome analysis of the EV71 5 ' untranslated region in differentiated neuronal cells SH-SY5Y and regulatory role of FBP3 in viral replication
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Interactome analysis of the EV71 5 ' untranslated region in differentiated neuronal cells SH-SY5Y and regulatory role of FBP3 in viral replication

机译:分化的神经元细胞SH-SY5Y中EV71 5'非翻译区的相互作用研究以及FBP3在病毒复制中的调控作用

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摘要

Enterovirus 71 (EV71), a single-stranded RNA virus, is one of the most serious neurotropic pathogens in the Asia-Pacific region. Through interactions with host proteins, the 5' untranslated region (5'UTR) of EV71 is important for viral replication. To gain a protein profile that interact with the EV71 5'UTR in neuronal cells, we performed a biotinylated RNA-protein pull-down assay in conjunction with LC-MS/MS analysis. A total of 109 proteins were detected and subjected to Database for Annotation, Visualization and Integrated Discovery (DAVID) analyses. These proteins were found to be highly correlated with biological processes including RNA processing/splicing, epidermal cell differentiation, and protein folding. Aprotein-protein interaction network was constructed using the STRING online database to illustrate the interactions of those proteins that are mainly involved in RNA processing/splicing or protein folding. Moreover, we confirmed that the far-upstream element binding protein 3 (FBP3) was able to bind to the EV71 5'UTR. The redistribution of FBP3 in subcellular compartments was observed after EV71 infection, and the decreased expression of FBP3 in host neuronal cells markedly inhibited viral replication. Our results reveal various host proteins that potentially interact with the EV71 5'UTR in neuronal cells, and we found that FBP3 could serve as a positive regulator in host cells.
机译:肠病毒71(EV71)是一种单链RNA病毒,是亚太地区最严重的嗜神经性病原体之一。通过与宿主蛋白的相互作用,EV71的5'非翻译区(5'UTR)对于病毒复制很重要。为了获得与神经元细胞中的EV71 5'UTR相互作用的蛋白质谱,我们结合LC-MS / MS分析进行了生物素化的RNA蛋白质下拉测定。总共检测到109种蛋白质,并进行了数据库的注释,可视化和综合发现(DAVID)分析。发现这些蛋白质与生物学过程高度相关,包括RNA加工/剪接,表皮细胞分化和蛋白质折叠。使用STRING在线数据库构建了一个蛋白质-蛋白质相互作用网络,以说明那些主要参与RNA加工/剪接或蛋白质折叠的蛋白质之间的相互作用。此外,我们证实了远上游元件结合蛋白3(FBP3)能够与EV71 5'UTR结合。 EV71感染后,观察到FBP3在亚细胞区室中的重新分布,并且宿主神经元细胞中FBP3表达的降低明显抑制了病毒复制。我们的研究结果揭示了可能与神经元细胞中的EV71 5'UTR相互作用的各种宿主蛋白​​,并且我们发现FBP3可以充当宿主细胞中的正调节剂。

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