通过网膜和蛋白质分泌来控制ER质量
Cathena Meiling Li1, Yong-Keun Jung1
1School of Biological Sciences, Seoul National University, Seoul, Korea.
Autophagy
|November 27, 2024
概括
研究人员发现,蛋白质FKBPL调节了网膜,即清除内质网膜 (ER) 组成部分的过程. FKBPL-CKAP4相互作用是ER质量控制的关键,并影响蛋白质分泌.
科学领域:
- 细胞生物学 细胞生物学
- 分子生物学分子生物学
- 自自是一种自的过程.
背景情况:
- 细胞内膜网膜 (ER) 对于细胞功能和平衡至关重要.
- 保持ER质量控制对于细胞生存至关重要.
研究的目的:
- 为了确定网络的新型调节者,ER的选择性自.
- 阐明FKBPL控制网膜和蛋白质分泌的分子机制.
主要方法:
- 基于形态的功能获取屏幕被用来识别FKBPL.
- 用蛋白结合测试和细胞成像来研究FKBPL-CKAP4相互作用.
- 研究了FKBPL-CKAP4轴中断对网膜和蛋白质分泌的影响.
主要成果:
- 鉴定FKBPL是一种细胞系调节器的网膜.
- FKBPL 结合于 ER 居民的 CKAP4,将 ER 桥接到光体,以进行 lysosomal 降解.
- FKBPL-CKAP4轴对基底性和压力诱导的网膜变都至关重要.
- 破坏FKBPL-CKAP4相互作用会损害网膜和增加通过微粒细胞的蛋白质分泌.
结论:
- FKBPL-CKAP4轴在调节网球方面发挥着至关重要的作用.
- 这个轴也影响细胞蛋白质分泌通路.
- 在ER质量控制和蛋白质分泌方面,FKBPL-CKAP4具有双重功能.
相关概念视频
Protein Folding Quality Check in the RER
3.7K
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...
3.7K
Export of Misfolded Proteins out of the ER
3.5K
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...
3.5K
ER Retrieval Pathway
3.8K
In the secretory pathway, vesicles transport proteins from one cellular compartment to another in forward transport to deliver the protein to its correct location. Occasionally, misfolded proteins and incorrect proteins escape their original compartments, and a retrieval pathway is used to return the escaped proteins to their original compartment.
The ER uses many checkpoints to prevent the entry of incorrectly folded or a resident protein as cargo onto a transport vesicle. These mechanisms...
The ER uses many checkpoints to prevent the entry of incorrectly folded or a resident protein as cargo onto a transport vesicle. These mechanisms...
3.8K
Post-translational Translocation of Proteins to the RER
5.6K
A sizable fraction of proteins destined for ER are first synthesized in the cell cytosol and then transported across the ER membrane–a process called post-translational translocation. Similar to cotranslationally translocated proteins, these proteins also use the Sec translocon complex to enter the ER lumen.
Targeting proteins to the ER
Hsp40 and Hsp70 chaperone molecules bind the translated proteins in the cytosol to prevent their folding. The chaperone binding helps to keep the signal...
Targeting proteins to the ER
Hsp40 and Hsp70 chaperone molecules bind the translated proteins in the cytosol to prevent their folding. The chaperone binding helps to keep the signal...
5.6K
Cotranslational Protein Translocation
7.2K
Translocation of proteins across membranes is an ancient process that occurs even in bacteria and archaebacteria. In fact, the components of the translocation machinery are still conserved between prokaryotes and eukaryotes.
Sec61 channel partners for cotranslational translocation
During cotranslational translocation, the Sec61 channel partners with the signal recognition particle (SRP), the signal recognition particle receptor (SR), and the ribosomes to transport the nascent polypeptide chain...
Sec61 channel partners for cotranslational translocation
During cotranslational translocation, the Sec61 channel partners with the signal recognition particle (SRP), the signal recognition particle receptor (SR), and the ribosomes to transport the nascent polypeptide chain...
7.2K
Recycling Endosomes and Transcytosis
2.6K
The recycling endosome, also known as the endosomal recycling compartment (ERC), is a part of the slow-recycling process of the endocytic pathway. Molecules internalized through receptor-mediated endocytosis are either degraded in the lysosomes or are recycled to the plasma membrane through the fast- or slow-recycling route.
The recycling endosome is not a single organelle but an extensively tubulated network of recycling pathways. It functions in storing molecules or transporting them across...
The recycling endosome is not a single organelle but an extensively tubulated network of recycling pathways. It functions in storing molecules or transporting them across...
2.6K


