Comprehensive Profiling of N‑Linked Glycosylation Sites in HeLa Cells Using Hydrazide Enrichment
Abstract
The adenocarcinoma cell line HeLa serves as a model system for cancer research in general and cervical cancer in particular. In this study, hydrazide enrichment in combination with state-of-the art nanoLC−MS/MS analysis was used to profile N-linked glycosites in HeLa cells. N-Linked glycoproteins were selectively enriched in HeLa cells by the hydrazide capture method, which isolates all glycoproteins independent of their glycans. Nonglycosylated proteins were removed by extensive washing. N-Linked glycoproteins were identified with the specific NXT/S motif and deamidated asparagine (N). Deglycosylation was carried out in both H_2 (^16)O and H_2 ^(18)O to confirm the deamidation. NanoLC−MS/MS analysis indicated that the method selectively enriched at least 100 fold N-linked glycosites in HeLa cells. When both the membrane and cytosolic fractions were used, a total of 268 unique N-glycosylation sites were identified corresponding to 106 glycoproteins. Bioinformatic analysis revealed that most of the glycoproteins identified are known to have an impact on cancer and have been proposed as biomarkers.
Additional Information
© 2012 American Chemical Society. Published In Issue January 04, 2013; Article ASAP December 04, 2012; Just Accepted Manuscript November 23, 2012; Received: July 18, 2012. The Norwegian Research council (Project 197431/F20) (H.M.), the Faculty of Mathematics and Natural Sciences at the University of Oslo (H.M.), the Betty and Gordon Moore Foundation (R.L.J.G., M.S., S.H.), and the Beckman Institute (M.S., S.H.) are acknowledged for their financial support. We thank Ruth Huettenhain (ETHZ) for critical reading of the manuscript. The authors declare no competing financial interest.Attached Files
Published - pr300859k.pdf
Supplemental Material - Malerod_SupplementalData3_Spectra.pdf
Supplemental Material - Malerod_Supplementary_Data_1_Tables_S1-S8.xlsx
Supplemental Material - pr300859k_si_002.pdf
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Additional details
- Eprint ID
- 37250
- Resolver ID
- CaltechAUTHORS:20130301-124120701
- 197431/F20
- Norwegian Research Council
- University of Oslo
- Gordon and Betty Moore Foundation
- Caltech Beckman Institute
- Created
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2013-03-02Created from EPrint's datestamp field
- Updated
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2021-11-09Created from EPrint's last_modified field