一种新型ER膜蛋白调节与ER相关的内分体裂变
Melissa J Hoyer1, Patrick J Chitwood1, Christopher C Ebmeier1
1Department of Molecular, Cellular, and Developmental Biology, University of Colorado-Boulder, Boulder, CO 80309, USA.
Cell
|September 18, 2018
概括
细胞内 (ER) 膜接触点对于内分裂至关重要. 由冠状病毒1C招募的ER蛋白TMCC1调节了这个过程,以进行适当的货物分类.
科学领域:
- 细胞生物学
- 分子生物学
- 膜贩运活动
背景情况:
- 细胞膜接触点 (MCS) 是细胞关键结点.
- 这些部位参与了内分体分裂和货物分类的调节.
- 在这些事件中ER的确切作用仍然不完全理解.
研究的目的:
- 确定参与MCS内核分裂的ER蛋白质.
- 阐明ER如何影响内芽和货物分类的机制.
- 确定这些部位的ER蛋白和actin调节器之间的关系.
主要方法:
- 采用杂交的生物酶策略来识别内基因芽上相互作用的ER蛋白.
- 使用siRNA评估已识别的蛋白质功能的耗尽研究.
- 免疫光显微镜可视化蛋白质定位和内体形态.
- 研究了冠状素1C在ER招募和actin依赖裂变中的作用.
主要成果:
- 确定了在ER内体MCS中缩的ER膜蛋白TMCC1.
- TMCC1 枯竭会损害与 ER 相关的内分体芽裂变和货物分类到戈尔吉.
- 冠状素1C对于TMCC1在ER内体接触部位的招募至关重要.
- 需要冠状蛋白1C来分类依赖于actin的货物的与ER相关的裂变.
结论:
- TMCC1 是一个关键的ER居住蛋白调节MCS的内分体裂变.
- TMCC1在ER内体接触部位的招募取决于冠状素1C.
- 这种相互作用突出了内分体裂变过程中ER参与货物分类的规范机制.
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