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From the Cover: AAA ATPase p97/VCP is essential for TRIM21-mediated virus neutralization

机译:从封面开始:AAA ATPase p97 / VCP对于TRIM21介导的病毒中和至关重要

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摘要

Tripartite motif-containing 21 (TRIM21) is a cytosolic IgG receptor that mediates intracellular virus neutralization by antibody. TRIM21 targets virions for destruction in the proteasome, but it is unclear how a substrate as large as a viral capsid is degraded. Here, we identify the ATPase p97/valosin-containing protein (VCP), an enzyme with segregase and unfoldase activity, as a key player in this process. Depletion or catalytic inhibition of VCP prevents capsid degradation and reduces neutralization. VCP is required concurrently with the proteasome, as addition of inhibitor after proteasomal degradation has no effect. Moreover, our results suggest that it is the challenging nature of virus as a substrate that necessitates involvement of VCP, since intracellularly expressed IgG Fc is degraded in a VCP-independent manner. These results implicate VCP as an important host factor in antiviral immunity.
机译:包含三方基序的21(TRIM21)是一种介导抗体对细胞内病毒中和的胞浆IgG受体。 TRIM21靶向病毒粒子以在蛋白酶体中进行破坏,但尚不清楚如何降解与病毒衣壳一样大的底物。在这里,我们确定了具有segregase和unfoldase活性的酶ATPase p97 /含valosin的蛋白质(VCP)是此过程的关键参与者。 VCP的耗尽或催化抑制可防止衣壳降解并减少中和作用。蛋白酶体同时需要VCP,因为蛋白酶体降解后添加抑制剂无效。此外,我们的结果表明,病毒作为底物的挑战性性质要求VCP的参与,因为细胞内表达的IgG Fc以不依赖VCP的方式降解。这些结果表明,VCP是抗病毒免疫的重要宿主因子。

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