This protocol describes the identification and quantification of phosphopeptides during the dynamic formation of an immunological synapse. Isotope-labeled immune and target cells are mixed, cell-to-cell conjugates are stabilized by cross-linking, and isolated by fluorescence-activated cell sorting (FACS). Phosphopeptides are isolated by phosphopeptide enrichment and measured by mass spectrometry. The resulting data are analyzed to separate cell-specific phosphopeptides using the isotope label and quantified by label-free quantification (LFQ).
[doi:10.25345/C5P26Q78C]
[dataset license: CC0 1.0 Universal (CC0 1.0)]
Keywords: Natural killer ; breast cancer ; phosphoproteomics ; SILAC ; Label free quantification
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Principal Investigators: (in alphabetical order) |
Daniel Perez Hernandez, Luxembourg Institute of Health, Luxembourg Gunnar Dittmar, Luxembourg Institute of Health, Luxembourg |
| Submitting User: | dperezh |
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Differential Proteins:
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Quantified Proteins:
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