在内质网膜中进行蛋白质折叠所需的基因的全面表征
Martin C Jonikas1, Sean R Collins, Vladimir Denic
1Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, CA 94143, USA.
概括
研究人员确定了参与蛋白质折叠的关键酵母基因,这些基因参与了内质网膜 (ER) 内的蛋白质折叠. 这项研究揭示了对ER功能和蛋白质加工至关重要的新蛋白质复合体,为疾病和衰老提供了洞察力.
科学领域:
- 细胞生物学 细胞生物学
- 分子生物学分子生物学
- 遗传学 是一个遗传学.
背景情况:
- 细胞内膜网 (ER) 中蛋白质错误折叠与衰老和各种疾病有关.
- 展开的蛋白质反应 (UPR) 是一种细胞应激途径,可以监测ER折叠状态.
研究的目的:
- 用UPR作为传感器识别参与ER蛋白折叠的基因.
- 通过遗传相互作用系统地绘制这些基因之间的功能关系.
主要方法:
- 使用定量报告器对酵母中展开的蛋白质反应 (UPR) 进行了全面的选.
- 对双重突变体中UPR水平的分析,以表征基因相互依赖.
主要成果:
- 确定了数百个酵母基因,这些基因对ER折叠至关重要.
- 发现对后来的分泌途径有很强的依赖.
- 发现了一种新的六蛋白跨膜复合体.
- 标志着一个参与尾部定蛋白质插入的协伴复合体.
结论:
- 这项研究揭示了ER蛋白折叠所必需的保存因素.
- 这种系统基因分析方法可用于剖析复杂的细胞过程.
- 这些发现为了解疾病和衰老中的ER功能障碍提供了基础.
相关概念视频
Protein Folding Quality Check in the RER
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...
Export of Misfolded Proteins out of the ER
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...
Regulation of the Unfolded Protein Response
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...
The Unfolded Protein Response
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...
Directing Proteins to the Rough Endoplasmic Reticulum
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...
Protein Modifications in the RER
Modification of secretory and transmembrane proteins entering the rough ER begins in the ER lumen. These modifications aid in protein folding and stabilize the acquired tertiary structure. Protein modifications in the rough ER co-occur at different stages of protein folding.
Broadly, these modifications can be categorized into four main categories — glycosylation, formation of disulfide bonds, assembly of protein subunits, and specific proteolytic cleavages like removal of signal sequences.
Broadly, these modifications can be categorized into four main categories — glycosylation, formation of disulfide bonds, assembly of protein subunits, and specific proteolytic cleavages like removal of signal sequences.


