协同转移的基化对黄病毒生物发生是必不可少的
Ranen Aviner1,2, Kathy H Li3, Judith Frydman4
1Department of Microbiology and Immunology, University of California, San Francisco, San Francisco, CA, USA.
Nature
|August 19, 2021
概括
像脊髓灰质炎,登革热和寨卡病毒这样的病毒通过改变蛋白质制造的复合体, 劫持宿主细胞机械. 针对这些病毒多体提供了一种新的抗病毒策略.
科学领域:
- 病毒学
- 分子生物学
- 生物化学
背景情况:
- 病毒病原体对全球公共健康构成重大威胁.
- 了解病毒与宿主之间的相互作用对于开发抗病毒疗法至关重要.
- 主体生物合成途径对于病毒复制至关重要.
研究的目的:
- 研究肠道病毒和病毒如何重塑宿主多体.
- 识别病毒用于蛋白质合成的宿主机械.
- 探索针对病毒多体作为一种抗病毒策略.
主要方法:
- 多种体的蛋白质组分析.
- 功能性基因组学
- 药物干预
- 病毒蛋白修饰的分析.
主要成果:
- 病毒感染 (脊髓灰质炎,登革热,寨卡病毒) 改变了多细胞组合,但并没有改变核糖体积.
- 病毒驱逐共同的转化因子并招募特定的宿主机器.
- 寨卡病毒和登革热病毒利用原蛋白氧化进行病毒多蛋白修饰.
- 抑制普罗林氧化会破坏病毒多蛋白折叠并减少病毒的产生.
结论:
- 病毒多体重塑是病毒与宿主界面上的一个模块化过程.
- 针对专门的病毒多体是一种有前途的抗病毒干预方法.
- 氧化是登革热和寨卡病毒利用的关键宿主因素.
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