克拉特林介导的内细胞分裂中的力量再分配,由卷轴式卷轴力传感器揭示出来
Yuan Ren1,2, Jie Yang3, Barbara Fujita1,2
1Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT, 06520, USA.
Science advances
|October 13, 2023
概括
研究人员开发了新的传感器,用于测量细胞内核细胞分裂期间的分子力. 他们发现End4p蛋白的作用力在内细胞机械上有所不同,揭示了力量再分配.
科学领域:
- 细胞生物学 细胞生物学
- 生物物理学的生物物理.
- 分子力学分子力学
背景情况:
- 在生物体内测量分子级别的力量是具有挑战性的.
- 细胞过程,如克拉特林介导的内细胞分裂,涉及细胞骨力量传递到等离子体膜.
- 精确的力量涉及到内细胞分裂仍然在很大程度上是未知的.
研究的目的:
- 开发用于分子尺度测量的新型体内力传感器.
- 在裂变酵母中通过克拉介导的内细胞分裂过程中量化作用于End4p蛋白的力量.
- 了解力量是如何在内细胞机械中传递和重新分配的.
主要方法:
- 开发新的基于蛋白质凝聚的体内力传感器.
- 应用传感器来测量End4p上的力量,End4p是一种将膜与actin细胞骨连接在一起的蛋白质.
- 力量测量是在内细胞机械的不同位置进行的.
主要成果:
- 在actin细胞骨附近,End4p经历了大约19个皮科纽顿的力.
- 在End4p上的力量大约在克拉特林网格附近为11皮科纽顿.
- 在等离子体膜附近,End4p在约9皮科纽顿的力下.
结论:
- 这项研究成功地量化了内细胞分裂期间的体内分子力量.
- 力量被收集并重新分配到内细胞蛋白质复合体中.
- 这些发现为推动细胞膜变形的机械力量提供了新的见解.
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