IκB激酶阻碍聚合:化TDP-43进行降解
Cha Yang1, Yanru Liu1, Fenghua Hu1
1Department of Molecular Biology and Genetics, Weill Institute for Cell and Molecular Biology, Cornell University, Ithaca, NY, USA.
The Journal of cell biology
|January 22, 2024
概括
炎症媒介IκB激酶 (IKK) 在细胞质中酸化TDP-43,促进其降解. 这一发现揭示了炎症途径与神经退行症中TDP-43蛋白水平调节之间的新鲜联系.
科学领域:
- 神经生物学 神经生物学 神经生物学
- 分子生物学分子生物学
- 细胞生物学 细胞生物学
背景情况:
- TDP-43聚合是各种神经退行性疾病的关键病理特征.
- 调节TDP-43蛋白水平并防止其聚合的精确机制尚未完全理解.
研究的目的:
- 研究炎症信号在TDP-43调节中的作用.
- 确定控制TDP-43酸化和降解的上游监管机构.
主要方法:
- 神经退行症的细胞模型
- 免疫阻塞是指免疫阻塞.
- 酸化部位的映射绘制
- 蛋白质体降解试验.
主要成果:
- IκB激酶 (IKK) 在特定的细胞质部位直接化TDP-43.
- 通过IKK的酸化向TDP-43进行蛋白质体降解.
- 这一过程将炎症信号与TDP-43平衡联系起来.
结论:
- 通过IKK介导的酸化代表了TDP-43清除的新途径.
- 针对IKK可以为与TDP-43病理相关的神经退行性疾病提供治疗策略.
相关概念视频
Regulation of the Unfolded Protein Response
2.4K
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...
2.4K
Regulated Protein Degradation
7.3K
It is vital to regulate the activity of enzymatic as well as non-enzymatic proteins inside the cell. This can be achieved either through creating a balance between their rate of synthesis and degradation or regulating the intrinsic activity of the protein. Both these regulation mechanisms play an essential role in the normal functioning of cells.
Protein degradation plays two important roles in the cells. It helps to protect cells from misfolded or damaged proteins before they lead to a...
Protein degradation plays two important roles in the cells. It helps to protect cells from misfolded or damaged proteins before they lead to a...
7.3K
The Unfolded Protein Response
4.6K
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...
4.6K
PI3K/mTOR/AKT Signaling Pathway
3.6K
The mammalian target of rapamycin (mTOR) is a serine/threonine kinase that regulates growth, proliferation, and cell survival in response to hormones, growth factors, or nutrient availability. This kinase exists in two structurally and functionally distinct forms: mTOR complex 1 (mTORC1) and mTOR complex 2 (mTORC2). The first form (mTORC1) is composed of a rapamycin-sensitive Raptor and proline-rich Akt substrate, PRAS40. In contrast, mTORC2 consists of a...
3.6K
Destabilization of Microtubules
2.7K
The destabilization of microtubules can occur during different stages of the microtubule lifecycle, such as nucleation or elongation. It can take place at either end of the microtubule or in the microtubule lattices as a whole. The lifespan of individual microtubules within a cell varies according to the cell type and stage of the cell cycle. During interphase, the lifespan of the microtubule is about 30 minutes, while during cell division, it is about 15 minutes. In axonal microtubules of...
2.7K
The Proteasome
845
Eukaryotic cells can degrade proteins through several pathways. One of the most important among these is the ubiquitin-proteasome pathway. It helps the cell eliminate the misfolded, damaged, or unwarranted cytoplasmic proteins in a highly specific manner.
In this pathway, the target proteins are first tagged with small proteins called ubiquitin. This involves participation of a series of enzymes including— E1 (ubiquitin-activating enzyme), E2 (ubiquitin-conjugating enzyme), and E3...
In this pathway, the target proteins are first tagged with small proteins called ubiquitin. This involves participation of a series of enzymes including— E1 (ubiquitin-activating enzyme), E2 (ubiquitin-conjugating enzyme), and E3...
845


