Zhang Zhuojun, Jiang Lili
Affiliated Cancer Hospital & Institute of Guangzhou Medical University, Guangzhou, China.
Guangzhou Municipal and Guangdong Provincial Key Laboratory of Protein Modification and Degradation, School of Basic Medical Science, Guangzhou Medical University, Guangzhou, China.
Methods Mol Biol. 2023;2712:135-148. doi: 10.1007/978-1-0716-3433-2_12.
The ubiquitin-proteasome system (UPS) is a highly conserved cellular mechanism that degrades and recycles proteins in eukaryotic cells. It involves the tagging of specific target proteins with ubiquitin, a small regulatory protein, which marks them for degradation by the proteasome, a large protein complex that acts as a molecular shredder. Dysfunction of the UPS has been implicated in a wide range of diseases, including cancer, neurodegenerative disorders, and viral infections. Therefore, targeting the UPS has become an attractive therapeutic strategy for many diseases. Ferroptosis is an iron-dependent cell death process that is regulated by multiple levels, including protein degradation. In this chapter, we introduce the detection of UPS-mediated protein degradation in ferroptosis using several techniques such as western blotting, co-immunoprecipitation, in vitro ubiquitination assay, and proteasome assay.
泛素-蛋白酶体系统(UPS)是一种高度保守的细胞机制,负责真核细胞中蛋白质的降解和循环利用。它涉及用泛素(一种小的调节蛋白)标记特定的靶蛋白,泛素会将这些蛋白标记为蛋白酶体降解的对象,蛋白酶体是一种大型蛋白质复合体,起着分子切碎机的作用。UPS功能失调与多种疾病有关,包括癌症、神经退行性疾病和病毒感染。因此,针对UPS已成为许多疾病有吸引力的治疗策略。铁死亡是一种铁依赖性细胞死亡过程,受到包括蛋白质降解在内的多个层面的调节。在本章中,我们介绍了使用蛋白质印迹法、免疫共沉淀法、体外泛素化测定法和蛋白酶体测定法等几种技术检测铁死亡中UPS介导的蛋白质降解。