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Incorporation of the Kaposi’s sarcoma-associated herpesvirus capsid vertex-specific component (CVSC) into self-assembled capsids

机译:将卡波西氏肉瘤相关疱疹病毒衣壳顶点特异性成分(CVSC)整合到自组装衣壳中

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摘要

Self-assembly of herpesvirus capsids can be accomplished in heterologous expression systems provided all six capsid proteins are present. We have demonstrated the assembly of icosahedral Kaposi’s sarcoma-associated herpesvirus (KSHV) capsids in insect cells using the baculovirus expression system. Using this self-assembly system we investigated whether we could add additional capsid associated proteins and determine their incorporation into the assembled capsid. We chose the capsid vertex-specific component (CVSC) proteins encoded by open reading frames (ORFs) 19 and 32 to test this. This complex sits on the capsid vertex and is important for capsid maturation in herpesvirus-infected cells. Co-immunoprecipitation assays were used to initially confirm a bi-molecular interaction between ORF19 and ORF32. Both proteins also precipitated the triplex proteins of the capsid shell (ORF26 and ORF62) as well as the major capsid protein (ORF25). Capsid immunoprecipitation assays revealed the incorporation of ORF19 as well as ORF32 into assembled capsids. Similar experiments also showed that the incorporation of each protein occurred independent of the other. These studies reveal biochemically how the KSHV CVSC interacts with the capsid shell.
机译:只要存在全部六个衣壳蛋白,疱疹病毒衣壳的自组装就可以在异源表达系统中完成。我们已经证明了使用杆状病毒表达系统在昆虫细胞中组装二十面体卡波西氏肉瘤相关疱疹病毒(KSHV)衣壳。使用这种自组装系统,我们研究了是否可以添加额外的衣壳相关蛋白,并确定它们是否结合到已组装的衣壳中。我们选择了由开放阅读框(ORF)19和32编码的衣壳顶点特定成分(CVSC)蛋白进行测试。该复合物位于衣壳顶上,对于疱疹病毒感染细胞的衣壳成熟至关重要。共免疫沉淀测定法最初用于确认ORF19和ORF32之间的双分子相互作用。两种蛋白质还沉淀了衣壳外壳的三链体蛋白质(ORF26和ORF62)以及主要衣壳蛋白质(ORF25)。衣壳免疫沉淀测定法揭示了将ORF19和ORF32掺入组装的衣壳中。相似的实验还表明,每种蛋白质的掺入均独立于另一种蛋白质。这些研究从化学上揭示了KSHV CVSC如何与衣壳相互作用。

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