竞争性蛋白质-RNA相互作用网络控制多相细胞内组织
David W Sanders1, Nancy Kedersha2, Daniel S W Lee1
1Department of Chemical and Biological Engineering, Princeton University, Princeton, NJ 08544, USA.
Cell
|April 18, 2020
概括
液相分离 (LLPS) 形成细胞凝结物. 竞争的蛋白质网络,而不是RNA结合,控制凝结物组成和共存,为了解细胞组织提供了一个新的框架.
科学领域:
- 生物物理
- 细胞生物学
- 分子生物学
背景情况:
- 通过液相分离 (LLPS) 形成无膜凝聚物.
- 生物物理规则控制凝聚剂组装,基层结构和共存并未完全理解.
- 细胞质应力颗粒 (SG) 和P体是这种凝结物的关键例子.
研究的目的:
- 阐明细胞凝聚物的多相组织的生物物理机制.
- 调查控制SG和P体的组成和可混合性的因素.
- 为了解可调节的冷凝物形成制定一个一般框架.
主要方法:
- 人类细胞中SG和P体的定量溶解.
- 蛋白相互作用网络和RNA结合域 (RBD) 的分析.
- 应用不一致的合物理论原则.
主要成果:
- 连接节点的蛋白质网络竞争,而不是RNA结合特异性或无序段,决定了SG和P体的组成和可混合性.
- 不连接的蛋白质的竞争性结合阻止了LLPS.
- 一个基于竞争网络的框架解释了可调节的冷凝物形成.
结论:
- 多相凝聚物组织是由蛋白质网络之间的静态测量依赖的竞争决定的.
- 这种竞争提供了一种可调节的机制,用于产生特定组成的冷凝物.
- 提出的框架提供了关于细胞分离的基础原则.
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