Fast Global Phosphoproteome Profiling of Jurkat T cells by HIFU-TiO2-SCX-LC-MS/MS
2017
Carrera, Mónica | Cañas, Benito | López-Ferrer, Daniel
10 pages, 6 figures, 1 table
显示更多 [+] 显示较少 [-]We propose a new workflow for fast phosphoproteome profiling. The workflow is based on the use of accelerated in-solution trypsin digestion under an ultrasonic field provided by high-intensity focused ultrasound (HIFU) combined with an inverse strategy based on TiO2 selective phosphopeptide enrichment, fractionation by strong cation exchange chromatography (SCX) and analysis by liquid chromatography tandem mass spectrometry (LC-MS/MS) using a high-resolution mass spectrometer. The performance of the method was established for the global phosphoproteome analysis of un-stimulated human Jurkat leukemia T cells (E6.1). Using this accelerated workflow, 15,367 phosphorylation sites from 13,029 different phosphopeptides belonging to 3,163 different phosphoproteins were efficiently identified with high-throughput and reproducibility in less than 15 h. The functional analysis revealed significant phosphorylation-based networks that are implicated in immune function and tumor development pathways. The present strategy, HIFU-TiO2-SCX-LC-MS/MS, is the fastest analytical method reported to date for generating large-scale phosphoproteomics datasets (<15 h)
显示更多 [+] 显示较少 [-]This work was supported by the EU Marie Curie actions (FP7-PEOPLE-2012-IEF, ref. 332274) and by the Ramón Areces Foundation (XVII National grant)
显示更多 [+] 显示较少 [-]Peer reviewed
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