结构切换动态控制双重伪结的罗斯肉瘤病毒编程的核糖体框架转移元件
Christopher P Jones1, Adrian R Ferré-D'Amaré1
1Laboratory of Nucleic Acids, Biochemistry and Biophysics Center, National Heart, Lung and Blood Institute, Bethesda, MD 20892-8012.
概括
逆转录病毒中编程的移,对于病毒蛋白平衡至关重要,由RNA结构控制. 研究人员解决了关键移元件的3D结构,揭示了这个过程中至关重要的动态双伪点.
科学领域:
- 结构生物学是结构生物学.
- 病毒学 病毒学
- 分子生物学分子生物学
背景情况:
- 编程的-1转移对于逆转录病毒复制至关重要,控制病毒蛋白质静态度.
- 来自罗斯肉瘤病毒的第一个发现的移刺激元素的3D结构在40年内仍然难以捉摸.
研究的目的:
- 为了确定罗斯肉瘤病毒的3D结构,转移的刺激元素.
- 阐明这个元素在调节编程移的结构-功能关系.
主要方法:
- 低温电子显微镜 (cryo-electron microscopy) (低温电子显微镜) 是一种电子显微镜.
- 在X射线晶体学.
- 结构-功能分析分析.
主要成果:
- RNA元素采用类似蝶的双重伪结折叠.
- 一个关键的氨酸残留物 (A2546) 起到切换作用,切换形状并影响移效率高达50倍.
- 结构揭示了形状异质性和动态交叉点.
结论:
- 动态的双伪结结构通过利用形状异质性来刺激框架转移.
- 支持一个多态模型,其中高的香农增强了移,是支持的.
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