翻译启动由RNA折叠动力学通过核糖体起草机制控制
Amin Espah Borujeni1, Howard M Salis1
1Department of Chemical Engineering and ‡Department of Biological Engineering, The Pennsylvania State University , University Park, Pennsylvania 16802, United States.
Journal of the American Chemical Society
|May 21, 2016
概括
核糖体起草是一种新的机制,在核糖体与mRNA快速结合之前,加速蛋白质合成. 这种不平衡的过程可以改变蛋白质的产生速度1000倍,
科学领域:
- 分子生物学
- 生物物理
- 系统生物学
背景情况:
- RNA折叠对于细胞过程至关重要,包括蛋白质合成.
- 目前的模型往往忽略了不平衡的RNA折叠对翻译的影响.
- 在平衡条件下主要研究翻译启动率.
研究的目的:
- 介绍并解释"核糖体起草"机制.
- 研究RNA折叠动力学和核糖体结合如何集体控制翻译.
- 探索非平衡RNA折叠对蛋白质合成速度的影响.
主要方法:
- 具有不同的核糖体结合率和折叠特性的mRNA的计算设计.
- 与时间相关的单光子计数以研究RNA折叠动态.
- 测量基因表达以量化蛋白质合成速率.
主要成果:
- 证明慢折叠与快折叠的RNA结构可以产生1000倍的蛋白质合成速率差异,即使具有相似的折叠能量.
- 通过表征mRNA属性,确定了核糖体起草所需的条件.
- 来自非平衡马尔科夫转换模型的验证预测.
结论:
- 核糖体起草是控制翻译启动的关键不平衡机制.
- 竞争性折叠和组装动力学显著影响基因表达序列-结构-功能关系.
- 这些发现对了解细胞基因表达机制具有广泛的意义.
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