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The Assembly of Ebola Virus Nucleocapsid Requires Virion-Associated Proteins 35 and 24 and Posttranslational Modification of Nucleoprotein

机译:埃博拉病毒核衣壳的大会需要与病毒颗粒相关的蛋白35和24和核蛋白的翻译后修饰。

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Ebola virus encodes seven viral structural and regulatory proteins that support its high rates of replication, but little is known about nucleocapsid assembly of this virus in infected cells. We reports here that three viral proteins are necessary and sufficient for formation of Ebola virus particles and that intracellular posttranslational modification regulates this process. Expression of the nucleoprotein (NP) and virion-associated proteins VP35 and VP24 led to spontaneous assembly of nucleocapsids in transfected 293T cells by transmission electron microscopy. A specific biochemical interaction of these three proteins was demonstrated, and, interestingly, O-glycosylation and sialation of NP were demonstrated and necessary for their association. This distinct mechanism of regulation for filovirus assembly suggests new approaches for viral therapies and vaccines for Ebola and related viruses.
机译:埃博拉病毒编码了七个支持其高复制率的病毒结构和调节蛋白,但对该病毒在感染细胞中的核衣壳组装了解甚少。我们在这里报告说,三种病毒蛋白对于埃博拉病毒颗粒的形成是必要和充分的,并且细胞内翻译后修饰调节了这一过程。核蛋白(NP)和病毒体相关蛋白VP35和VP24的表达导致通过透射电子显微镜在转染的293T细胞中自发组装核衣壳。证明了这三种蛋白质的特异性生化相互作用,有趣的是,证明了NP的O-糖基化和唾液酸化并且对于它们的结合是必需的。丝状病毒装配的这种独特的调节机制为埃博拉病毒和相关病毒的病毒疗法和疫苗提供了新的方法。

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