Huang Wenxuan, Qiu Yanping, Huynh Diana, Wang Ting-Yu, Chou Tsui-Fen
Biology and Biological Engineering, California Institute of Technology, Pasadena, California, United States.
Proteome Exploration Laboratory, Beckman Institute, California Institute of Technology, Pasadena, California, United States.
MicroPubl Biol. 2024 Nov 27;2024. doi: 10.17912/micropub.biology.001372. eCollection 2024.
Human p97/VCP is a vital AAA ATPase (ATPase associated with diverse cellular activity) that plays critical roles in protein homeostasis by regulating autophagy, endosomal trafficking, and the ubiquitin-proteasome system. Global proteomics analysis of p97/VCP inhibition with CB-5083 has been performed in HCT116 colon cells. Here, we examined the impact of CB-5083 treatment in another cancer model, the HL-60 acute myeloid leukemia cell line, employing subcellular fractionation combined with label-free proteomics to analyze changes in protein levels across cytoplasmic, nuclear, and insoluble membrane protein compartments. The results reveal distinct compartment-specific protein regulation, providing insight into p97/VCP's cellular mechanisms and its potential for targeted therapeutic applications.
人类p97/VCP是一种重要的AAA型ATP酶(与多种细胞活动相关的ATP酶),通过调节自噬、内体运输和泛素-蛋白酶体系统在蛋白质稳态中发挥关键作用。已在HCT116结肠细胞中对CB-5083抑制p97/VCP进行了全局蛋白质组学分析。在此,我们在另一种癌症模型HL-60急性髓系白血病细胞系中研究了CB-5083处理的影响,采用亚细胞分级分离结合无标记蛋白质组学来分析细胞质、细胞核和不溶性膜蛋白区室中蛋白质水平的变化。结果揭示了不同区室特异性的蛋白质调控,为了解p97/VCP的细胞机制及其在靶向治疗应用中的潜力提供了见解。