在内质网膜中的UFM1:将ER应激,核糖体质量控制和ER-phagy联系起来
Masaaki Komatsu1,2, Gaoxin Mao1
1Department of Physiology, Juntendo University Graduate School of Medicine, Japan.
Essays in biochemistry
|October 9, 2025
概括
乌比奎丁折叠修饰剂1 (UFM1) 调节了内细胞网膜 (ER) 蛋白质质量控制. 这篇评论探讨了UFM1的情况.
科学领域:
- 细胞生物学 细胞生物学
- 分子生物学分子生物学
- 生物化学 生物化学
背景情况:
- 乌比奎丁折叠修饰剂1 (UFM1) 是一种类似于乌比奎丁的蛋白质.
- UFM1是蛋白质稳定的一个关键调节器,维持蛋白质稳定.
- 细胞内膜网膜 (ER) 是UFM1活动的中心部位.
研究的目的:
- 审查UFM1在ER质量控制中的作用.
- 探索细胞应激期间的UFM1调节.
- 讨论UFM1参与ER相关的降解和自.
主要方法:
- 关于UFM1研究的文献综述.
- 对UFM1参与ER应激反应的分析.
- 检查UFM1在核糖体相关质量控制和ER自中的作用.
主要成果:
- UFM1协调与核糖体相关的质量控制和ER选择性自.
- 在细胞应激期间,UFM1通路受到调节.
- 干扰UFM1功能与疾病有关,特别是在神经系统.
结论:
- UFM1对于保持ER健康和蛋白质质量至关重要.
- 了解UFM1的机制,可以了解疾病的发病性.
- 对UFM1调节和功能的进一步研究是有必要的.
相关概念视频
The Unfolded Protein Response
6.2K
The ER is the hub of protein synthesis in a cell. It has robust systems to quality control protein folding and also for degradation of terminally misfolded proteins. Under normal conditions, a small proportion of misfolded proteins that cannot be salvaged need to be transported to the cytoplasm by the ER-associated degradation or ERAD pathways. However, if the ERAD cannot handle the misfolded proteins, the cell activates the unfolded protein response or UPR to adjust the protein folding...
6.2K
Export of Misfolded Proteins out of the ER
5.0K
After folding, the ER assesses the quality of secretory and membrane proteins. The correctly folded proteins are cleared by the calnexin cycle for transport to their final destination, while misfolded proteins are held back in the ER lumen. The ER chaperones attempt to unfold and refold the misfolded proteins but sometimes fail to achieve the correct native conformation. Such terminally misfolded proteins are then exported to the cytosol by ER-associated degradation or ERAD pathway for...
5.0K
Regulation of the Unfolded Protein Response
2.9K
Inositol-requiring kinase one or IRE1 is the most conserved eukaryotic unfolded protein response (UPR) receptor. It is a type I transmembrane protein kinase receptor with a distinctive site-specific RNase activity. As the binding mechanics of the misfolded proteins with the N-terminal domain of IRE-1 are unclear, three binding models — direct, indirect, and allosteric -- are proposed for receptor activation. Nevertheless, it is known that once a misfolded protein associates with IRE1, it...
2.9K
Protein Folding Quality Check in the RER
5.0K
ER is the primary site for the maturation and folding of soluble and transmembrane secretory proteins. The calnexin cycle is a specific chaperone system that folds and assesses the confirmation of N-glycosylated proteins before they can exit the ER lumen. The primary players of this quality check pipeline are the lectins, ER-resident chaperones, and a glucosyl transferase enzyme. In case the calnexin system in the lumen fails to salvage a misfolded protein, it is transported to the cytoplasm...
5.0K
Role of ER in the Secretory Pathway
6.9K
Eukaryotic cells have a special pathway that enables communication between various intracellular membrane-bound compartments and also with the extracellular environment. This pathway is termed as the secretory pathway.
Components of the secretory pathway
About a third of proteins synthesized in the cell are sorted via the secretory route. They shuffle between different compartments in membrane-bound vesicles until they reach their final destination. The main intracellular compartments involved...
Components of the secretory pathway
About a third of proteins synthesized in the cell are sorted via the secretory route. They shuffle between different compartments in membrane-bound vesicles until they reach their final destination. The main intracellular compartments involved...
6.9K
Directing Proteins to the Rough Endoplasmic Reticulum
16.9K
The organelle-specific signaling sequences direct proteins synthesized in the cytosol to their final destination like ER, mitochondria, peroxisomes, etc. Some of the proteins directed to ER are then trafficked via vesicles to other organelles within the cell or the extracellular environment through the Golgi complex. For example, the rough ER synthesizes soluble proteins for transportation to the lysosomes or secretion out of the cell. It can also synthesize transmembrane proteins that can...
16.9K


