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Large Scale Localization of ProteinPhosphorylation by Use of Electron Capture Dissociation Mass Spectrometry Steve M. M. Sweet?§, Christopher M. Bailey?§, Debbie L. Cunningham?§,John K. Heath?§, and Helen J. Cooper§? From the ?Cancer Research UK Growth Factor Group, §School of Biosciences, College of Life and Environmental Sciences, University of Birmingham, Edgbaston, Birmingham B15 2TT, United Kingdom 2. Experiment procedures 3. Analysis of Results Summary of phosphopeptides identified from both DD-CID-ECD and NL-ECD experiments. The results indicate that phosphopeptides constituted 40–45% of the starting mixture. It should be noted that not every phosphopeptide identified by CID triggered an ECD event. FIG. 1. Overlap between DTAs leading to identifications by ECD and CID. All 4763 identifications IDs are from paired CID/ECD events .FIG. 2. Overlap between distinct phosphopeptides identified by ECD and CID. All 1220 identifications are from paired CID/ECDevents. FIG. 3. Binned distribution of SLoMo scores. The x axis has log scale. All identifications are from paired CID/ECD events. Identifications with only one possible site of localization are not included. FIG. 4. Overlap between distinct, well localized SLoMo 19 phosphopeptides identified by ECD and CID. All 725 identifications are from paired CID/ECD events. Identifications with only one possible localization are not included. FIG. 5. Example of isomeric phosphopeptide co-elution. a, ECD mass spectrum showing first and third serine phosphorylation SLoMo score, 21.5 . b, CID mass spectrum showing evidence for threonine phosphorylation SLoMo score, 24.3 . The site of phosphorylation indicated by SLoMo is shown uppermost inset in b. FIG. 6. Multiply phosphorylated peptides identified and localized from ECD and CID mass spectra and sorted by charge state. All identifications are from paired events. Identifications with only one possible localization are not included. 4. Conclusion In this study we anal
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