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Cryo-Electron Microscopy Structure of Adenovirus Type 2 Temperature-Sensitive Mutant 1 Reveals Insight into the Cell Entry Defect

机译:2型腺病毒温度敏感突变体1的低温电子显微镜结构揭示了对细胞进入缺陷的了解。

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摘要

The structure of the adenovirus type 2 temperature-sensitive mutant 1 (Ad2ts1) was determined to a resolution of 10 Å by cryo-electron microscopy single-particle reconstruction. Ad2ts1 was prepared at a nonpermissive temperature and contains the precursor forms of the capsid proteins IIIa, VI, and VIII; the core proteins VII, X (mu), and terminal protein (TP); and the L1-52K protein. Cell entry studies have shown that although Ad2ts1 can bind the coxsackievirus and Ad receptor and undergo internalization via αv integrins, this mutant does not escape from the early endosome and is targeted for degradation. Comparison of the Ad2ts1 structure to that of mature Ad indicates that Ad2ts1 has a different core architecture. The Ad2ts1 core is closely associated with the icosahedral capsid, a connection which may be mediated by preproteins IIIa and VI. Density within hexon cavities is assigned to preprotein VI, and membrane disruption assays show that hexon shields the lytic activity of both the mature and precursor forms of protein VI. The internal surface of the penton base in Ad2ts1 appears to be anchored to the core by interactions with preprotein IIIa. Our structural analyses suggest that these connections to the core inhibit the release of the vertex proteins and lead to the cell entry defect of Ad2ts1.
机译:通过冷冻电子显微镜单颗粒重建将2型腺病毒温度敏感突变体1(Ad2ts1)的结构确定为10Å的分辨率。 Ad2ts1是在非许可温度下制备的,含有衣壳蛋白IIIa,VI和VIII的前体形式;核心蛋白VII,X(μ)和末端蛋白(TP);和L1-52K蛋白。细胞进入研究表明,尽管Ad2ts1可以结合柯萨奇病毒和Ad受体并通过αv整合素进行内在化,但该突变体不会从早期的内体中逃逸出来,并被靶向降解。 Ad2ts1结构与成熟Ad的结构比较表明,Ad2ts1具有不同的核心架构。 Ad2ts1核心与二十面体衣壳紧密相关,该连接可能由前蛋白IIIa和VI介导。六邻体腔内的密度分配给了前蛋白质VI,膜破坏分析表明六邻体同时屏蔽了蛋白质VI成熟形式和前体形式的裂解活性。 Ad2ts1中的戊烯碱基的内表面似乎通过与前蛋白IIIa的相互作用而锚定在核心上。我们的结构分析表明,这些与核心的连接会抑制顶点蛋白的释放,并导致Ad2ts1的细胞进入缺陷。

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