mTORC1通过调节拥挤控制细胞质的相分离和生物物理性质
M Delarue1, G P Brittingham1, S Pfeffer2
1Institute for Systems Genetics, New York University Langone Health, New York, NY 10016, USA.
Cell
|June 26, 2018
概括
遗传编码的多重纳米粒子揭示了mTORC1通路如何通过调节核糖体度来控制细胞拥挤. 这会影响细胞内的物理性质和相分离.
科学领域:
- 细胞生物物理学
- 分子生物学
- 系统生物学
背景情况:
- 大分子拥挤显著影响细胞反应速率和物理性质.
- 控制细胞拥挤的精确机制在很大程度上是未知的.
研究的目的:
- 研究细胞内的宏分子拥挤的调节机制.
- 了解mTORC1途径在细胞质特性调节中的作用.
主要方法:
- 开发用于跟踪的基因编码多重纳米粒子 (GEM).
- 使用GEM与遗传和药理方法相结合.
- 测量粒子和分子运动的有效扩散系数.
主要成果:
- 通过核糖体度变化,mTORC1途径对≥20nm颗粒的扩散进行了超过2倍的调节.
- 没有观察到对≤5nm分子运动的显著影响.
- 改变的核糖体度在体外和体内都影响了相分离.
结论:
- mTORC1途径在控制细胞质中介尺度生物物理性质方面发挥着关键作用.
- 核糖体度是mTORC1调节的关键因素,影响细胞质特性和生物分子凝聚.
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