尼迪西斯特罗病毒IRES驱动,启动因子独立的翻译的结构研究揭示了真核生物翻译延长的关键步骤
Swastik De1, Clara G Altomare1,2, Irina S Abaeva3
1Department of Biochemistry and Molecular Biophysics, Columbia University, New York, NY 10032, USA.
bioRxiv : the preprint server for biology
|November 19, 2025
概括
这项研究揭示了使用NediV IRES启动病毒翻译的结构机制. 它详细介绍了IRES从启动到延伸的过渡过程,包括核糖体校对.
科学领域:
- 结构生物学 结构生物学
- 病毒学 病毒学
- 分子生物学分子生物学
背景情况:
- 内部核糖体进入点 (IRES) 能够在病毒中启动独立于cap的翻译.
- 了解IRES的功能对于病毒复制和宿主-病原体相互作用至关重要.
研究的目的:
- 确定80S核糖体的高分辨率结构与NediV IRES复合在各种功能状态下.
- 阐明IRES介导的翻译启动及其过渡到正规延长的机制细节.
主要方法:
- 高分辨率冷电子显微镜 (cryo-EM) 用于可视化核糖体复合体.
- 对二进制复合体,氨基酸-tRNA结合复合体和具有延长因子的复合体进行结构分析.
主要成果:
- 在二进制复合体中,NediV IRES主要占据了核糖体P位,显示出形状灵活性.
- 结构重组,包括PKI领域的不稳定,促进过渡到延长.
- 可视化了eEF2结合和eEF1A结合的复合体,包括一个对校对后复合体与不匹配的tRNA,没有捕获剂.
结论:
- 提供了IGR IRES介导的翻译启动和延长的全面结构概述.
- 揭示了对病毒翻译和核糖体校对过程的关键机制性见解.
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