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相关概念视频

Protein Translocation Machinery on the ER Membrane01:28

Protein Translocation Machinery on the ER Membrane

4.7K
The translocon complex situated on the ER membrane is the main gateway for the protein secretory pathway. It facilitates the transport of nascent peptides into the ER lumen and their insertion into the ER membrane.
Sec61 protein conducting channel
In eukaryotes, the translocon complex comprises a core heterotrimeric translocator channel called the Sec61 complex. This channel includes three transmembrane proteins, Sec61α, Sec61β, and Sec61γ, and is the largest subunit of the...
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Directing Proteins to the Rough Endoplasmic Reticulum01:34

Directing Proteins to the Rough Endoplasmic Reticulum

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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...
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Export of Misfolded Proteins out of the ER01:32

Export of Misfolded Proteins out of the ER

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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...
3.7K
ER Retrieval Pathway01:45

ER Retrieval Pathway

3.9K
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...
3.9K
The Endoplasmic Reticulum01:43

The Endoplasmic Reticulum

15.0K
The endoplasmic reticulum or ER makes up for more than half of the membranes in a cell and accounts for 10% of total cell volume. It is also the primary protein and lipid synthesis factory for most cell organelles, such as the Golgi apparatus, lysosomes, secretory vesicles, and the plasma membrane. Despite being the most extensive and functionally complex subcellular organelle, ER was the last to be discovered. After years of deliberation, Keith Porter and George Palade in the year 1954,...
15.0K
Assembly of the Lipid Bilayer in the ER01:28

Assembly of the Lipid Bilayer in the ER

3.2K
Biological membranes are more than just a barrier separating cell cytoplasm from the outside environment. They are highly dynamic and help maintain the integrity and physiological stability of the cells as well as membrane-bound organelles. Membranes also play vital roles in cell-to-cell and intracellular communication.
A large chunk of any biological membrane is composed of phospholipids. These lipids have a heterogeneous distribution across different subcellular organelles and even between...
3.2K

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相关实验视频

Updated: Jul 23, 2025

Visualization of Endoplasmic Reticulum Subdomains in Cultured Cells
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Visualization of Endoplasmic Reticulum Subdomains in Cultured Cells

Published on: February 18, 2014

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追逐正确的尾巴:ER膜综合体如何识别其基质

Doron Rapaport1, Johannes M Herrmann2

  • 1Interfaculty Institute of Biochemistry, University of Tübingen, Tübingen, Germany.

The Journal of cell biology
|July 12, 2023
PubMed
概括
此摘要是机器生成的。

ER 膜综合体 (EMC) 专门将尾部定蛋白质插入到内质网膜中. 它使用电荷依赖过器来确保正确的蛋白质拓,并防止线粒体蛋白质的错误插入.

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Visualization and Quantification of Endogenous Intra-Organelle Protein Interactions at ER-Mitochondria Contact Sites by Proximity Ligation Assays
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Purification of the Membrane Compartment for Endoplasmic Reticulum-associated Degradation of Exogenous Antigens in Cross-presentation
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Purification of the Membrane Compartment for Endoplasmic Reticulum-associated Degradation of Exogenous Antigens in Cross-presentation

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相关实验视频

Last Updated: Jul 23, 2025

Visualization of Endoplasmic Reticulum Subdomains in Cultured Cells
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Visualization of Endoplasmic Reticulum Subdomains in Cultured Cells

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Visualization and Quantification of Endogenous Intra-Organelle Protein Interactions at ER-Mitochondria Contact Sites by Proximity Ligation Assays
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Visualization and Quantification of Endogenous Intra-Organelle Protein Interactions at ER-Mitochondria Contact Sites by Proximity Ligation Assays

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Purification of the Membrane Compartment for Endoplasmic Reticulum-associated Degradation of Exogenous Antigens in Cross-presentation
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Purification of the Membrane Compartment for Endoplasmic Reticulum-associated Degradation of Exogenous Antigens in Cross-presentation

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科学领域:

  • 细胞生物学 细胞生物学
  • 分子生物学分子生物学
  • 贩卖蛋白质 贩卖蛋白质 是一个问题.

背景情况:

  • 尾部定蛋白质对于各种细胞功能至关重要,它们可以插入诸如ER,线粒体和过氧体等有机体的膜.
  • 尾部定蛋白质的适当定位对于细胞平衡和功能至关重要.

研究的目的:

  • 研究ER膜复合体 (EMC) 介导尾蛋白质插入ER膜的机制.
  • 确定EMC如何区分ER向蛋白和其他尾部定蛋白,例如用于线粒体的蛋白.

主要方法:

  • 使用生物化学分析来研究蛋白质插入到ER膜.
  • 研究了基于电荷的相互作用在蛋白质向和插入中的作用.
  • 分析了EMC对具有不同拓信号的尾蛋白质的选择性.

主要成果:

  • 该ER膜复合体 (EMC) 具有内在的依赖电荷的选择性过器.
  • 这种过器特别促进了基于其拓信号的ER尾蛋白质的插入.
  • 该EMC有效地防止线粒体尾部定蛋白质错误地纳入ER膜.

结论:

  • 该EMC在确保尾部定蛋白质在细胞内的正确定位方面发挥着至关重要的作用.
  • 电磁中心的取决于电荷的选择性过器是维持有机细胞膜完整性和功能的关键.
  • 了解这种机制可以了解蛋白质贩运和有机体生物发生.