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Targeted Online Liquid Chromatography Electron Capture Dissociation Mass Spectrometry for the Localization of Sites of in Vivo Phosphorylation in Human Sprouty2
Author(s) -
Steve M. M. Sweet,
Faraz K. Mardakheh,
Kevin J. P. Ryan,
Amy J. Langton,
John K. Heath,
Helen J. Cooper
Publication year - 2008
Publication title -
analytical chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.117
H-Index - 332
eISSN - 1520-6882
pISSN - 0003-2700
DOI - 10.1021/ac800963a
Subject(s) - chemistry , phosphopeptide , phosphorylation , mass spectrometry , dissociation (chemistry) , chromatography , isobaric labeling , in vivo , isobaric process , biophysics , tandem mass spectrometry , biochemistry , protein mass spectrometry , microbiology and biotechnology , biology , physics , thermodynamics
We demonstrate a strategy employing collision-induced dissociation for phosphopeptide discovery, followed by targeted electron capture dissociation (ECD) for site localization. The high mass accuracy and low background noise of the ECD mass spectra allow facile sequencing of coeluting isobaric phosphopeptides, with up to two isobaric phosphopeptides sequenced from a single mass spectrum. In contrast to the previously described neutral loss dependent ECD method, targeted ECD allows analysis of both phosphotyrosine peptides and lower abundance phosphopeptides. The approach was applied to phosphorylation analysis of human Sprouty2, a regulator of receptor tyrosine kinase signaling. Fifteen sites of phosphorylation were identified, 11 of which are novel.

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