氧化是一种低估的翻译后修改,与酸化变化相关的免疫反应调节
Isabel Karkossa1, Sabine Fürst1, Henning Großkopf1
1Department of Molecular Systems Biology, Helmholtz-Centre for Environmental Research - UFZ, Leipzig, Germany.
Frontiers in immunology
|October 9, 2023
概括
氧化是一种关键的翻译后修饰,影响巨细胞激活和炎症反应. 这项研究在全球范围内绘制了氧化位点的地图,揭示了它们与酸化的共同调节以及在类似收费类受体4信号传导等途径中的重要作用.
科学领域:
- 免疫学 免疫学 免疫学
- 蛋白质组学是指蛋白质组学.
- 后翻译修改 后翻译修改
背景情况:
- 巨细胞是重要的免疫细胞,受到氧化还原状态的影响.
- 作为免疫细胞的翻译后修饰 (PTM) 的氧化还未得到充分的认识.
- 巨细胞的全球氧化数据仍然很少.
研究的目的:
- 全球评估氧化对巨细胞激活的影响.
- 研究氧化,酸化和蛋白质表达之间的相互作用.
- 为了确定免疫反应中氧化驱动的调节机制.
主要方法:
- 使用非向蛋白质组学和PTM-omics.
- 在用脂多糖 (LPS) 刺激的THP-1巨细胞上应用了序列性iodoTMT标签.
- 综合了来自10,452个氧化位点,5,057个蛋白质和7,148个酸化位点的数据.
主要成果:
- 确定了10,452个氧化位点,揭示了免疫相关途径的显著变化,例如收费类受体4 (TLR4) 信号传递.
- 在炎症途径中观察到氧化和酸化之间的共同调节.
- 与蛋白质和酸化部位相比,检测到氧化部位的时间依赖动态.
结论:
- 氧化在调节炎症过程和巨细胞激活方面发挥着重要作用.
- 这项研究提供了一个强大的方法,用于全球还原组分析.
- 强调考虑与其他PTM一起氧化的重要性,以全面了解免疫细胞功能的重要性.
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