Department of Molecular Biology, Princeton University, Princeton, New Jersey;
Mol Cell Proteomics. 2013 Nov;12(11):3237-52. doi: 10.1074/mcp.M113.030866. Epub 2013 Aug 12.
Much like the host cells they infect, viruses must also regulate their life cycles. Herpes simples virus type 1 (HSV-1), a prominent human pathogen, uses a promoter-rich genome in conjunction with multiple viral trans-activating factors. Following entry into host cells, the virion-associated outer tegument proteins pUL46 and pUL47 act to increase expression of viral immediate-early (α) genes, thereby helping initiate the infection life cycle. Because pUL46 has gone largely unstudied, we employed a hybrid mass spectrometry-based approach to determine how pUL46 exerts its functions during early stages of infection. For a spatio-temporal characterization of pUL46, time-lapse microscopy was performed in live cells to define its dynamic localization from 2 to 24 h postinfection. Next, pUL46-containing protein complexes were immunoaffinity purified during infection of human fibroblasts and analyzed by mass spectrometry to investigate virus-virus and virus-host interactions, as well as post-translational modifications. We demonstrated that pUL46 is heavily phosphorylated in at least 23 sites. One phosphorylation site matched the consensus 14-3-3 phospho-binding motif, consistent with our identification of 14-3-3 proteins and host and viral kinases as specific pUL46 interactions. Moreover, we determined that pUL46 specifically interacts with the viral E3 ubiquitin ligase ICP0. We demonstrated that pUL46 is partially degraded in a proteasome-mediated manner during infection, and that the catalytic activity of ICP0 is responsible for this degradation. This is the first evidence of a viral protein being targeted for degradation by another viral protein during HSV-1 infection. Together, these data indicate that pUL46 levels are tightly controlled and important for the temporal regulation of viral gene expression throughout the virus life cycle. The concept of a structural virion protein, pUL46, performing nonstructural roles is likely to reflect a theme common to many viruses, and a better understanding of these functions will be important for developing therapeutics.
与它们感染的宿主细胞非常相似,病毒也必须调节它们的生命周期。单纯疱疹病毒 1 型(HSV-1)是一种重要的人类病原体,它使用富含启动子的基因组和多种病毒转录激活因子。病毒进入宿主细胞后,衣壳相关的外被蛋白 pUL46 和 pUL47 作用于提高病毒即刻早期(α)基因的表达,从而帮助启动感染生命周期。由于 pUL46 很大程度上尚未被研究,我们采用了一种基于混合质谱的方法来确定 pUL46 在感染早期阶段如何发挥其功能。为了对 pUL46 进行时空特征分析,我们在活细胞中进行了延时显微镜观察,以确定其在感染后 2 至 24 小时的动态定位。接下来,我们在人成纤维细胞感染过程中通过免疫亲和纯化含有 pUL46 的蛋白复合物,并通过质谱分析来研究病毒-病毒和病毒-宿主相互作用以及翻译后修饰。我们证明 pUL46 在至少 23 个位点上被高度磷酸化。一个磷酸化位点与 14-3-3 磷酸结合模体的共识序列匹配,这与我们鉴定到 14-3-3 蛋白以及宿主和病毒激酶作为 pUL46 的特定相互作用物的结果一致。此外,我们确定 pUL46 特异性地与病毒 E3 泛素连接酶 ICP0 相互作用。我们证明 pUL46 在感染过程中以蛋白酶体介导的方式被部分降解,而 ICP0 的催化活性负责这种降解。这是在 HSV-1 感染过程中首次发现一种病毒蛋白被另一种病毒蛋白靶向降解的证据。总之,这些数据表明 pUL46 水平受到严格控制,对于整个病毒生命周期中病毒基因表达的时间调节非常重要。结构衣壳蛋白 pUL46 执行非结构功能的概念可能反映了许多病毒的一个共同主题,更好地理解这些功能对于开发治疗方法将非常重要。