Authors
Harald Marx, Simone Lemeer, Jan Erik Schliep, Lucrece Matheron, Shabaz Mohammed, Jürgen Cox, Matthias Mann, Albert JR Heck, Bernhard Kuster
Publication date
2013/6
Journal
Nature biotechnology
Volume
31
Issue
6
Pages
557-564
Publisher
Nature Publishing Group US
Description
We present a peptide library and data resource of >100,000 synthetic, unmodified peptides and their phosphorylated counterparts with known sequences and phosphorylation sites. Analysis of the library by mass spectrometry yielded a data set that we used to evaluate the merits of different search engines (Mascot and Andromeda) and fragmentation methods (beam-type collision-induced dissociation (HCD) and electron transfer dissociation (ETD)) for peptide identification. We also compared the sensitivities and accuracies of phosphorylation-site localization tools (Mascot Delta Score, PTM score and phosphoRS), and we characterized the chromatographic behavior of peptides in the library. We found that HCD identified more peptides and phosphopeptides than did ETD, that phosphopeptides generally eluted later from reversed-phase columns and were easier to identify than unmodified peptides and that current …
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