TY - JOUR
T1 - Comparison of Enrichment Methods for Intact N- and O-Linked Glycopeptides Using Strong Anion Exchange and Hydrophilic Interaction Liquid Chromatography
AU - Yang, Weiming
AU - Shah, Punit
AU - Hu, Yingwei
AU - Toghi Eshghi, Shadi
AU - Sun, Shisheng
AU - Liu, Yang
AU - Zhang, Hui
N1 - Funding Information:
We thank Drs. Sergei Snovida and Julian Saba for providing protocol and discussion regarding the SAX cartridges. This work was supported by the National Institutes of Health, the National Institute of Allergy and Infectious Diseases (Grant R21AI122382), National Cancer Institute, the Early Detection Research Network (EDRN, Grant U01CA152813), the Clinical Proteomic Tumor Analysis Consortium (CPTAC, Grant U24CA160036), National Heart Lung and Blood Institute, Programs of Excellence in Glycosciences (PEG, Grant P01HL107153), by amfAR, The Foundation for AIDS Research on Bringing Bioengineers to Cure HIV (Grant amfAR 109551-61-RGRL), by Maryland Innovation Initiative (MII), and by The Patrick C. Walsh Prostate Cancer Research Fund.
Publisher Copyright:
© 2017 American Chemical Society.
PY - 2017/11/7
Y1 - 2017/11/7
N2 - Heterogeneity of protein glycosylation poses great challenges for analysis that is key to understand structure and function of glycoproteins. Resolving this conundrum requires efficient and specific enrichment of intact glycopeptides for identification and quantitation. To this end, hydrophilic interaction chromatography (HILIC) has been commonly used to enrich intact N- and O-linked glycopeptides. However, its effectiveness to enrich isobarically labeled glycopeptides remains unclear. Here, we studied three different enrichment methods for enrichment of N- and O-linked glycopeptides. It was found that removal of N-glycans prior to enrichment of O-linked glycopeptides by HILIC improved identification of O-linked glycopeptides by mass spectrometry. We also compared the enrichment of intact N- and O-linked glycopeptides using other chromatography methods and found that using cartridges containing materials for strong anion exchange (SAX) chromatography increased yield and identification of N- and O-linked glycopeptides. The enrichment of O-linked glycopeptides was further improved when a Retain AX cartridge (RAX) was used. In particular, isobaric tag labeled glycopeptides after C18 desalting could be readily enriched by SAX and RAX cartridges but not by HILIC to enable quantitative glycoproteomics. It is anticipated that the use of SAX and RAX cartridges will facilitate broad applications of identifications and quantitation of glycoproteins.
AB - Heterogeneity of protein glycosylation poses great challenges for analysis that is key to understand structure and function of glycoproteins. Resolving this conundrum requires efficient and specific enrichment of intact glycopeptides for identification and quantitation. To this end, hydrophilic interaction chromatography (HILIC) has been commonly used to enrich intact N- and O-linked glycopeptides. However, its effectiveness to enrich isobarically labeled glycopeptides remains unclear. Here, we studied three different enrichment methods for enrichment of N- and O-linked glycopeptides. It was found that removal of N-glycans prior to enrichment of O-linked glycopeptides by HILIC improved identification of O-linked glycopeptides by mass spectrometry. We also compared the enrichment of intact N- and O-linked glycopeptides using other chromatography methods and found that using cartridges containing materials for strong anion exchange (SAX) chromatography increased yield and identification of N- and O-linked glycopeptides. The enrichment of O-linked glycopeptides was further improved when a Retain AX cartridge (RAX) was used. In particular, isobaric tag labeled glycopeptides after C18 desalting could be readily enriched by SAX and RAX cartridges but not by HILIC to enable quantitative glycoproteomics. It is anticipated that the use of SAX and RAX cartridges will facilitate broad applications of identifications and quantitation of glycoproteins.
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U2 - 10.1021/acs.analchem.7b03641
DO - 10.1021/acs.analchem.7b03641
M3 - Article
C2 - 29016103
AN - SCOPUS:85046727919
SN - 0003-2700
VL - 89
SP - 11193
EP - 11197
JO - Analytical Chemistry
JF - Analytical Chemistry
IS - 21
ER -