TY - JOUR
T1 - Fragmentation of phosphopeptides by atmospheric pressure MALDI and ESI/ion trap mass spectrometry
AU - Moyer, Susanne C.
AU - Cotter, Robert J.
AU - Woods, Amina S.
N1 - Funding Information:
Funding for this work was provided by a contract (DABT63-99-1-0006) to RJC from the Defense Advanced Research Project Agency (DARPA) and from NIDA Intramural Research Program, NIDA, NIH. Support for SCM was provided by a NSF-GOALI grant (CHE 9634238). The authors wish to thank Andrew E. Taggi (Department of Chemistry, Johns Hopkins University) and Professor Douglas P. Ridge (Department of Chemistry and Biochemistry, University of Delaware) for their helpful discussions regarding this manuscript.
PY - 2002
Y1 - 2002
N2 - An investigation of phosphate loss from phosphopeptide ions was conducted, using both atmospheric pressure matrix-assisted laser desorption/ionization (AP MALDI) and electrospray ionization (ESI) coupled to an ion trap mass spectrometer (ITMS). These experiments were carried out on a number of phosphorylated peptides in order to investigate gas phase dephosphorylation patterns associated with phosphoserine, phosphothreonine, and phosphotyrosine residues. In particular, we explored the fragmentation patterns of phosphotyrosine containing peptides, which experience a loss of 98 Da under collision induced dissociation (CID) conditions in the ITMS. The loss of 98 Da is unexpected for phosphotyrosine, given the structure of its side chain. The fragmentation of phosphoserine and phosphothreonine containing peptides was also investigated. While phosphoserine and phosphothreonine residues undergo a loss of 98 Da under CID conditions regardless of peptide amino acid composition, phosphate loss from phosphotyrosine residues seems to be dependent on the presence of arginine or lysine residues in the peptide sequence.
AB - An investigation of phosphate loss from phosphopeptide ions was conducted, using both atmospheric pressure matrix-assisted laser desorption/ionization (AP MALDI) and electrospray ionization (ESI) coupled to an ion trap mass spectrometer (ITMS). These experiments were carried out on a number of phosphorylated peptides in order to investigate gas phase dephosphorylation patterns associated with phosphoserine, phosphothreonine, and phosphotyrosine residues. In particular, we explored the fragmentation patterns of phosphotyrosine containing peptides, which experience a loss of 98 Da under collision induced dissociation (CID) conditions in the ITMS. The loss of 98 Da is unexpected for phosphotyrosine, given the structure of its side chain. The fragmentation of phosphoserine and phosphothreonine containing peptides was also investigated. While phosphoserine and phosphothreonine residues undergo a loss of 98 Da under CID conditions regardless of peptide amino acid composition, phosphate loss from phosphotyrosine residues seems to be dependent on the presence of arginine or lysine residues in the peptide sequence.
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U2 - 10.1016/S1044-0305(01)00361-0
DO - 10.1016/S1044-0305(01)00361-0
M3 - Article
C2 - 11908807
AN - SCOPUS:0036112145
SN - 1044-0305
VL - 13
SP - 274
EP - 283
JO - Journal of the American Society for Mass Spectrometry
JF - Journal of the American Society for Mass Spectrometry
IS - 3
ER -