货物上的启动枢纽的相隔是选择性自的触发开关
Mariya Licheva1,2, Jeremy Pflaum3, Riccardo Babic1,2,4
1Institute of Biochemistry and Molecular Biology, ZBMZ, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Nature cell biology
|January 8, 2025
概括
细胞自,对于质量控制至关重要,是通过调节阶段分离启动. 这个过程在货物表面形成了启动枢纽,驱动了发酵孔核化,用于酵母和人体细胞中的降解.
科学领域:
- 细胞生物学 细胞生物学
- 分子生物学分子生物学
背景情况:
- 自是一种维持恒常状态和降解受损组件的基本细胞过程.
- 虽然批量自是非选择性的,但选择性的自通过自受体准特定的货物.
- 阶段分离在调节选择性自启动中的作用尚不清楚.
研究的目的:
- 研究阶段分离在选择性自开始过程中的作用.
- 了解自受体和载荷相互作用如何影响相位分离和自进展.
- 为了设计一种新的货物,通过选择性自来降解.
主要方法:
- 利用酵母和人类细胞模型来研究自.
- 研究了自启动枢纽的形成和动态.
- 分析了受体-载荷相互作用亲和力对相位分离和自的影响.
- 设计了一种哺乳动物的reovirus蛋白作为一种可降解的货物.
主要成果:
- 关键的自生物发生因子在酵母体的货物表面形成相隔的启动枢纽.
- 这些枢纽依赖于自受体和货物之间的多价值,低亲和相互作用.
- 高亲和相互作用抑制了枢纽形成和自.
- 在人类细胞中的各种货物上也观察到启动枢纽,将它们连接到内质网膜以进行光体组装.
- 改造后的reovirus蛋白 μNS成为了选择性自的目标.
结论:
- 调节相位分离是一种保守的机制,是大量和选择性自的基础.
- 自启动枢纽动态调节货物识别和孔核形成.
- 阶段分离的原理可以用来设计新的选择性自基质.
相关概念视频
Autophagy
4.2K
Autophagy is a self-digesting process by which a cell protects itself from threats both within and outside the cell, ranging from abnormal proteins to invading bacteria. In this process, obsolete components of the cell and invading microbes are degraded by hydrolytic enzymes active in an acidic environment of the lysosomal lumen.
An autophagic pathway consists of a series of signaling events activated in response to diverse stress and physiological conditions such as food deprivation,...
An autophagic pathway consists of a series of signaling events activated in response to diverse stress and physiological conditions such as food deprivation,...
4.2K
Autophagic Cell Death
3.4K
Christian de Duve discovered “autophagy,” a process in which cellular components are engulfed by membrane-bound organelles called autophagosomes. The autophagosomes then fuse with lysosomes to digest the enclosed contents. Autophagy is generally activated in cells to prevent cell death. However, cell death is triggered when the damage is beyond repair.
Autophagy and Apoptosis
Autophagy can activate apoptosis. In normal conditions, the autophagy activating protein Beclin-1 and...
Autophagy and Apoptosis
Autophagy can activate apoptosis. In normal conditions, the autophagy activating protein Beclin-1 and...
3.4K
Separation of Sister Chromatids
3.6K
At the transition from prophase to metaphase, there is a reduction in cohesion along the chromosomal arms, resulting in the resolution of sister chromatids. However, residual cohesin connections remain to hold the sister chromatids together until the transition from metaphase to anaphase. The residual connection prevents any premature separation of sister chromatids, blocking the risks of aneuploidy within the daughter cells.
At the onset of anaphase, separase, a proteolytic enzyme, is...
At the onset of anaphase, separase, a proteolytic enzyme, is...
3.6K
Delivery Pathways to the Lysosome
6.1K
Eukaryotic cells use different mechanisms to eliminate toxic waste obsolete and worn-out substances. Lysosomes play a pivotal role in this, and hence, these substances are carried to the lysosome from other parts of the cell and extracellular space through different pathways. The most elaborately studied pathways to the lysosome are the endocytic pathways.
Endocytosis
In endocytosis, the cell membrane takes up macromolecules and particles from the surrounding medium. Clathrin-mediated...
Endocytosis
In endocytosis, the cell membrane takes up macromolecules and particles from the surrounding medium. Clathrin-mediated...
6.1K
Anaphase Promoting Complex
2.8K
The stepwise destruction of specific proteins is necessary for the progression and completion of the cell cycle. Such proteins are ubiquitinated by ubiquitin ligases and then subsequently destroyed by the proteasome. The SCF (Skp1/Cullin/F-box) and the anaphase-promoting complex (APC) are two important ubiquitin ligases involved in cell cycle progression. While SCF is active throughout the cell cycle, APC gets activated during metaphase to anaphase transition. Cdc20 or Cdh1 binds to APC and...
2.8K
Pinching-off of Coated Vesicles
3.1K
Vesicle budding is orchestrated by distinct cytosolic proteins such as adaptor proteins, coat proteins, and GTPases. To initiate vesicle budding, membrane-bending proteins containing crescent-shaped BAR domains bind to the lipid heads in the bilayer and distort the membrane to form a protein-coated vesicle bud. Adaptors proteins such as AP2 for clathrin-coated vesicles can nucleate on the deformed membrane. Finally, coat proteins such as clathrin or COPI and COPII assemble into a coat forming...
3.1K


