蛋白质组学分析揭示了p97抑制剂CB-5083对HL-60细胞系不同细胞区室蛋白水平的差异影响。

microPublication biology Pub Date : 2024-11-27 eCollection Date: 2024-01-01 DOI:10.17912/micropub.biology.001372
Wenxuan Huang, Yanping Qiu, Diana Huynh, Ting-Yu Wang, Tsui-Fen Chou
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引用次数: 0

摘要

人类 p97/VCP 是一种重要的 AAA ATP 酶(与多种细胞活性相关的 ATP 酶),它通过调节自噬、内体转运和泛素-蛋白酶体系统在蛋白质稳态中发挥关键作用。在 HCT116 结肠细胞中进行了 CB-5083 抑制 p97/VCP 的全蛋白质组学分析。在这里,我们研究了 CB-5083 治疗对另一种癌症模型--HL-60 急性髓性白血病细胞系--的影响,采用亚细胞分馏结合无标记蛋白质组学分析了细胞质、细胞核和不溶性膜蛋白区室蛋白质水平的变化。研究结果揭示了不同区室的特异性蛋白调控,从而深入了解了 p97/VCP 的细胞机制及其靶向治疗应用潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Proteomics analysis reveals the differential impact of the p97 inhibitor CB-5083 on protein levels in various cellular compartments of the HL-60 cell line.

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.

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