蛋白质组
等压标记
等压法
串联质量标签
定量蛋白质组学
试剂
葡萄孢霉素
串联质谱法
计算生物学
化学
蛋白质组学
质谱法
生物
色谱法
生物信息学
生物化学
蛋白质质谱法
激酶
基因
物理化学
物理
蛋白激酶C
热力学
作者
Jiaming Li,Jonathan G. Van Vranken,Laura Pontano Vaites,Devin K. Schweppe,Edward L. Huttlin,Chris Etienne,Premchendar Nandhikonda,Rosa Viner,Aaron M. Robitaille,Andrew Thompson,Karsten Kuhn,Ian Pike,Ryan Bomgarden,John C. Rogers,Steven P. Gygi,João A. Paulo
出处
期刊:Nature Methods
[Nature Portfolio]
日期:2020-03-16
卷期号:17 (4): 399-404
被引量:469
标识
DOI:10.1038/s41592-020-0781-4
摘要
Isobaric labeling empowers proteome-wide expression measurements simultaneously across multiple samples. Here an expanded set of 16 isobaric reagents based on an isobutyl-proline immonium ion reporter structure (TMTpro) is presented. These reagents have similar characteristics to existing tandem mass tag reagents but with increased fragmentation efficiency and signal. In a proteome-scale example dataset, we compared eight common cell lines with and without Torin1 treatment with three replicates, quantifying more than 8,800 proteins (mean of 7.5 peptides per protein) per replicate with an analysis time of only 1.1 h per proteome. Finally, we modified the thermal stability assay to examine proteome-wide melting shifts after treatment with DMSO, 1 or 20 µM staurosporine with five replicates. This assay identified and dose-stratified staurosporine binding to 228 cellular kinases in just one, 18-h experiment. TMTpro reagents allow complex experimental designs—all with essentially no missing values across the 16 samples and no loss in quantitative integrity. A set of isobaric labeling reagents called TMTpro enables deep quantitative comparisons of proteome measurements across 16 samples.
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