Schmidt Alexander, Kochanowski Karl, Vedelaar Silke, Ahrné Erik, Volkmer Benjamin, Callipo Luciano, Knoops Kèvin, Bauer Manuel, Aebersold Ruedi, Heinemann Matthias
Biozentrum, University of Basel, Basel, Switzerland.
Institute of Molecular Systems Biology, ETH Zurich, Zurich, Switzerland.
Nat Biotechnol. 2016 Jan;34(1):104-10. doi: 10.1038/nbt.3418. Epub 2015 Dec 7.
Measuring precise concentrations of proteins can provide insights into biological processes. Here we use efficient protein extraction and sample fractionation, as well as state-of-the-art quantitative mass spectrometry techniques to generate a comprehensive, condition-dependent protein-abundance map for Escherichia coli. We measure cellular protein concentrations for 55% of predicted E. coli genes (>2,300 proteins) under 22 different experimental conditions and identify methylation and N-terminal protein acetylations previously not known to be prevalent in bacteria. We uncover system-wide proteome allocation, expression regulation and post-translational adaptations. These data provide a valuable resource for the systems biology and broader E. coli research communities.
测量蛋白质的精确浓度有助于深入了解生物过程。在此,我们采用高效的蛋白质提取和样品分级分离方法,以及最先进的定量质谱技术,为大肠杆菌生成了一张全面的、依赖于条件的蛋白质丰度图谱。我们在22种不同的实验条件下,对55%的预测大肠杆菌基因(超过2300种蛋白质)的细胞蛋白质浓度进行了测量,并鉴定出了此前未知在细菌中普遍存在的甲基化和N端蛋白质乙酰化修饰。我们揭示了全系统的蛋白质组分配、表达调控和翻译后适应性变化。这些数据为系统生物学和更广泛的大肠杆菌研究群体提供了宝贵的资源。