Abstract
Here we demonstrate quantitation of stimuli-induced proteome dynamics in primary cells by combining the power of bio-orthogonal noncanonical amino acid tagging (BONCAT) and stable-isotope labeling of amino acids in cell culture (SILAC). In conjunction with nanoscale liquid chromatography-tandem mass spectrometry (nanoLC-MS/MS), quantitative noncanonical amino acid tagging (QuaNCAT) allowed us to monitor the early expression changes of >600 proteins in primary resting T cells subjected to activation stimuli.
Original language | English |
---|---|
Pages (from-to) | 343-346 |
Number of pages | 4 |
Journal | Nature Methods |
Volume | 10 |
Issue number | 4 |
DOIs | |
Publication status | Published - 2013 |