TMTpro reagents: a set of isobaric labeling mass tags enables simultaneous proteome-wide measurements across 16 samples

被引:306
作者
Li, Jiaming [1 ]
Van Vranken, Jonathan G. [1 ]
Vaites, Laura Pontano [1 ]
Schweppe, Devin K. [1 ]
Huttlin, Edward L. [1 ]
Etienne, Chris [2 ]
Nandhikonda, Premchendar [2 ]
Viner, Rosa [3 ]
Robitaille, Aaron M. [3 ]
Thompson, Andrew H. [4 ]
Kuhn, Karsten [4 ]
Pike, Ian [4 ]
Bomgarden, Ryan D. [2 ]
Rogers, John C. [2 ]
Gygi, Steven P. [1 ]
Paulo, Joao A. [1 ]
机构
[1] Harvard Med Sch, Dept Cell Biol, Boston, MA 02115 USA
[2] Thermo Fisher Sci, Rockford, IL USA
[3] Thermo Fisher Sci, San Jose, CA USA
[4] Proteome Sci, London, England
关键词
RELATIVE QUANTIFICATION; QUANTITATIVE PROTEOMICS; STRATEGY; PHOSPHORYLATION; REVEALS; TARGET; MTOR;
D O I
10.1038/s41592-020-0781-4
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A set of isobaric labeling reagents called TMTpro enables deep quantitative comparisons of proteome measurements across 16 samples. 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 mu M 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.
引用
收藏
页码:399 / +
页数:12
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