TY - JOUR
T1 - Large-Scale Measurement of Absolute Protein Glycosylation Stoichiometry
AU - Sun, Shisheng
AU - Zhang, Hui
N1 - Publisher Copyright:
© 2015 American Chemical Society.
PY - 2015/7/7
Y1 - 2015/7/7
N2 - Protein glycosylation is one of the most important protein modifications. Glycosylation site occupancy alteration has been implicated in human diseases and cancers. However, current glycoproteomic methods focus on the identification and quantification of glycosylated peptides and glycosylation sites but not glycosylation occupancy or glycoform stoichiometry. Here we describe a method for large-scale determination of the absolute glycosylation stoichiometry using three independent relative ratios. Using this method, we determined 117 absolute N-glycosylation occupancies in OVCAR-3 cells. Finally, we investigated the possible functions and the determinants for partial glycosylation. (Graph Presented).
AB - Protein glycosylation is one of the most important protein modifications. Glycosylation site occupancy alteration has been implicated in human diseases and cancers. However, current glycoproteomic methods focus on the identification and quantification of glycosylated peptides and glycosylation sites but not glycosylation occupancy or glycoform stoichiometry. Here we describe a method for large-scale determination of the absolute glycosylation stoichiometry using three independent relative ratios. Using this method, we determined 117 absolute N-glycosylation occupancies in OVCAR-3 cells. Finally, we investigated the possible functions and the determinants for partial glycosylation. (Graph Presented).
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U2 - 10.1021/acs.analchem.5b01679
DO - 10.1021/acs.analchem.5b01679
M3 - Article
C2 - 26066578
AN - SCOPUS:84936797513
SN - 0003-2700
VL - 87
SP - 6479
EP - 6482
JO - Analytical Chemistry
JF - Analytical Chemistry
IS - 13
ER -