PNGaseF-Generated N-Glycans Adduct onto Peptides in the Gas Phase

Glycoproteomics has recently increased in popularity due to instrumental and methodological advances. That said, O-glycoproteomic analysis is still challenging for various reasons, including signal suppression, search algorithm limitations, and co-occupancy of N- and O-glycopeptides. To decrease sample complexity and simplify analysis, most O-glycoproteomic workflows include PNGaseF digestion, which is an endoglycosidase that removes most N-glycan structures. Here, we report that N-glycans released from PNGaseF digestion were identified during data acquisition and hampered detection of O-glycopeptides. Importantly, we noted instances where free glycans adducted to unmodified peptides in the gas phase and were misidentified by search algorithms as O-glycopeptides. We confirmed the presence of free glycans in other experiments performed in our laboratory, as well as from data generated by other groups. To overcome this limitation, we demonstrated that released N-glycans can be removed using a molecular weight cut off filter prior to (glyco)protease digestion, which improves O-glycoproteomic coverage.

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Publication Details

Journal
Journal of the American Society for Mass Spectrometry
Published
2025-02-12
DOI
https://doi.org/10.1021/jasms.4c00431
Primary Topic
Glycosylation and Glycoproteins Research
Type
article
Field-Weighted Citation Impact
0.00

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article

PNGaseF-Generated N-Glycans Adduct onto Peptides in the Gas Phase

Ryan Chen, Marie A. Hollenhorst, Valentina Rangel-Angarita, Stacy Alyse Malaker et al.
Journal of the American Society for Mass Spectrometry
Glycosylation and Glycoproteins Research
article

PNGaseF-Generated N-Glycans Adduct onto Peptides in the Gas Phase

Ryan Chen, Marie A. Hollenhorst, Valentina Rangel-Angarita, Stacy Alyse Malaker, Joann Chongsaritsinsuk, Alexandra D. Steigmeyer, Keira E. Mahoney, Akua A. Appah-Sampong, Isabella P. Tran, Lea M. Kim
article en

Abstract

Glycoproteomics has recently increased in popularity due to instrumental and methodological advances. That said, O-glycoproteomic analysis is still challenging for various reasons, including signal suppression, search algorithm limitations, and co-occupancy of N- and O-glycopeptides. To decrease sample complexity and simplify analysis, most O-glycoproteomic workflows include PNGaseF digestion, which is an endoglycosidase that removes most N-glycan structures. Here, we report that N-glycans released from PNGaseF digestion were identified during data acquisition and hampered detection of O-glycopeptides. Importantly, we noted instances where free glycans adducted to unmodified peptides in the gas phase and were misidentified by search algorithms as O-glycopeptides. We confirmed the presence of free glycans in other experiments performed in our laboratory, as well as from data generated by other groups. To overcome this limitation, we demonstrated that released N-glycans can be removed using a molecular weight cut off filter prior to (glyco)protease digestion, which improves O-glycoproteomic coverage.

Journal of the American Society for Mass SpectrometryVol. 36(3)
Brigham and Women's Hospital (US), Harvard University (US), Yale University (US)
Cancer Research Institute, Yale University, National Heart, Lung, and Blood Institute, National Institute of General Medical Sciences
Openalex Percentile: Top 98%
Glycosylation and Glycoproteins Research
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PNGaseF-Generated N-Glycans Adduct onto Peptides in the Gas Phase — Ryan Chen, Marie A. Hollenhorst, et al. · Journal of the American Society for Mass Spectrometry (2025) | TGRS Research Map | TGRS