穿透蛋白在非外病毒上的功能重新折叠
Tobias Herrmann1,2, Raúl Torres3, Eric N Salgado3,4
1Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA, USA.
Nature
|January 14, 2021
概括
罗塔病毒使用VP4蛋白来创建细胞进入的膜损伤. 结构分析显示VP4的重组暴露了
科学领域:
- 病毒学
- 结构生物学
- 细胞生物学
背景情况:
- 没有外的病毒需要膜破坏才能进入细胞.
- 罗塔病毒通过病毒蛋白VP4进入宿主细胞.
研究的目的:
- 阐明罗塔病毒VP4蛋白透膜的分子机制.
- 在病毒进入过程中确定VP4的结构重组.
主要方法:
- 使用电子冷显微镜 (cryo-EM) 来确定轮状病毒表面上的VP4结构.
- 使用电子冷图,可视化病毒颗粒进入细胞.
- 使用VP4的二硫化物突变来稳定中间形状.
主要成果:
- 激活的VP4 (VP8*和VP5*) 经历了从"直立"到"倒置"状态的变化.
- "逆转"的VP4形状暴露了一个埋藏的"脚"域,它与宿主细胞膜相互作用.
- 低温图形数据支持VP4介导膜透的拟议机制.
结论:
- 这项研究定义了由VP4形状变化引发的轮状病毒透的分子机制.
- 这些发现表明VP4的作用机制可能与其他病毒进入途径有相似之处.
- 这项研究提供了关于轮状病毒感染早期的重要见解.
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