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黑色素瘤细胞中SUMO底物的广谱鉴定

Broad spectrum identification of SUMO substrates in melanoma cells.

作者信息

Ganesan Anand K, Kho Yoonjung, Kim Sung Chan, Chen Yue, Zhao Yingming, White Michael A

机构信息

Department of Dermatology, University of California, Irvine, CA 92697-2400, USA.

出版信息

Proteomics. 2007 Jun;7(13):2216-21. doi: 10.1002/pmic.200600971.

Abstract

Like phosphorylation, protein sumoylation likely represents a dynamic PTM to alter protein function in support of cell regulatory systems. The broad-spectrum impact of transient or chronic engagement of signal transduction cascades on protein sumoylation has not been explored. Here, we find that epidermal growth factor (EGF) stimulation evokes a rapid alteration in small ubiquitin modifier (SUMO) target selection, while oncogene expression alters steady-state SUMO-protein profiles. A proteomic SUMO target analysis in melanoma cells identified proteins involved in cellular signaling, growth control, and neural differentiation.

摘要

与磷酸化一样,蛋白质类泛素化修饰可能是一种动态的翻译后修饰,可改变蛋白质功能以支持细胞调节系统。信号转导级联反应的短暂或长期激活对蛋白质类泛素化修饰的广泛影响尚未得到研究。在此,我们发现表皮生长因子(EGF)刺激会引起小泛素样修饰物(SUMO)靶标选择的快速改变,而癌基因表达则会改变SUMO-蛋白质的稳态图谱。对黑色素瘤细胞进行的蛋白质组学SUMO靶标分析确定了参与细胞信号传导、生长控制和神经分化的蛋白质。

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