Journal
JOURNAL OF CHROMATOGRAPHY A
Volume 1172, Issue 1, Pages 9-18Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.chroma.2007.09.032
Keywords
phosphopeptide; phosphorylation; elation time; reversed-phase liquid chromatography; normalization; GRAVY; prediction capability
Funding
- NCRR NIH HHS [RR018522, P41 RR018522, P41 RR018522-03] Funding Source: Medline
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Elution time shifts between 33 different peptides and their corresponding phosphopeptides ranging from 4 amino acid residues to 35 amino acids in length were systematically investigated using high-resolution reversed-phase liquid chromatography (RPLC)-tandem mass spectrometry (MS/MS) analysis with trifluoroacetic acid as the ion pairing agent. Observed peptide elution time shifts for a single phosphorylation ranged from -5.28 min (for pYVPML) to +0.59 min (for HRDpSGLLDSLGR). Peptides containing a phosphotyrosine residue displayed a significant decrease in elution time following phosphorylation compared to their similar-sized peptides with phosphoserine or phosphothreonine residues. While peptide phosphorylation generally led to a decrease in the observed elution time, five peptides displayed increased elution times as a result of phosphorylation. For large peptides (>= 18 amino acids), the elution time shifts due to single phosphorylation were limited (ranging between -0.48 and +0.03 min), while the elution time shifts for small peptides (< 18 amino acids) were characterized by a larger deviation (ranging between -5.28 and +0.59 min). The predictive capability for the observed RPLC elution time change due to phosphorylation has been suggested, which will aid in assigning confident phosphopeptide identifications and their subsequent confirmation. (c) 2007 Elsevier B.V. All rights reserved.
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