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Absolute Quantitation of Glycosylation Site Occupancy Using Isotopically Labeled Standards and LC-MS

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Journal of The American Society for Mass Spectrometry

Abstract

N-linked glycans are required to maintain appropriate biological functions on proteins. Underglycosylation leads to many diseases in plants and animals; therefore, characterizing the extent of glycosylation on proteins is an important step in understanding, diagnosing, and treating diseases. To determine the glycosylation site occupancy, protein N-glycosidase F (PNGase F) is typically used to detach the glycan from the protein, during which the formerly glycosylated asparagine undergoes deamidation to become an aspartic acid. By comparing the abundance of the resulting peptide containing aspartic acid against the one containing non-glycosylated asparagine, the glycosylation site occupancy can be evaluated. However, this approach can give inaccurate results when spontaneous chemical deamidation of the non-glycosylated asparagine occurs. To overcome this limitation, we developed a new method to measure the glycosylation site occupancy that does not rely on converting glycosylated peptides to their deglycosylated forms. Specifically, the overall protein concentration and the non-glycosylated portion of the protein are quantified simultaneously by using heavy isotope-labeled internal standards coupled with LC-MS analysis, and the extent of site occupancy is accurately determined. The efficacy of the method was demonstrated by quantifying the occupancy of a glycosylation site on bovine fetuin. The developed method is the first work that measures the glycosylation site occupancy without using PNGase F, and it can be done in parallel with glycopeptide analysis because the glycan remains intact throughout the workflow.

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References

  1. Zhou, T., Xu, L., Dey, B., Hessell, A.J., Van Ryk, D., Xiang, S.-H., Yang, X., Zhang, M.-Y., Zwick, M.B., Arthos, J., Burton, D.R., Dimitrov, D.S., Sodroski, J., Wyatt, R., Nabel, G.J., Kwong, P.D.: Structural definition of a conserved neutralization epitope on HIV-1 gp120. Nature 445, 732–737 (2007)

    Article  CAS  Google Scholar 

  2. Drake, P.M., Cho, W., Li, B.S., Prakobphol, A., Johansen, E., Anderson, N.L., Regnier, F.E., Gibson, B.W., Fisher, S.J.: Sweetening the pot: adding glycosylation to the biomarker discovery equation. Clin. Chem. 56, 223–236 (2010)

    Article  CAS  Google Scholar 

  3. Jones, J., Krag, S.S., Betenbaugh, M.J.: Controlling N-linked glycan site occupancy. Biochim. Biophys. Acta 1726, 121–137 (2005)

    Article  CAS  Google Scholar 

  4. Petrescu, A.J., Milac, A.L., Petrescu, S.M., Dwek, R.A., Wormald, M.R.: Statistical analysis of the protein environment of N-glycosylation sites: implications for occupancy, structure, and folding. Glycobiology 14, 103–114 (2004)

    Article  CAS  Google Scholar 

  5. Hulsmeier, A.J., Paesold-Burda, P., Hennet, T.: N-glycosylation site occupancy in serum glycoproteins using multiple reaction monitoring liquid chromatography-mass spectrometry. Mol. Cell. Proteom. 6, 2132–2138 (2007)

    Article  CAS  Google Scholar 

  6. Ivancic, M.M., Gadgil, H.S., Halsall, H.B., Treuheit, M.J.: LC/MS analysis of complex multiglycosylated human alpha(1)-acid glycoprotein as a model for developing identification and quantitation methods for intact glycopeptide analysis. Anal. Biochem. 400, 25–32 (2010)

    Article  CAS  Google Scholar 

  7. Kuster, B., Mann, M.: O-18-labeling of N-glycosylation sites to improve the identification of gel-separated glycoproteins using peptide mass mapping and database searching. Anal. Chem. 71, 1431–1440 (1999)

    Article  CAS  Google Scholar 

  8. Segu, Z.M., Hussein, A., Novotny, M.V., Mechref, Y.: Assigning N-glycosylation sites of glycoproteins using LC/MSMS in conjunction with endo-M/exoglycosidase mixture. J. Proteome Res. 9, 3598–3607 (2010)

    Article  CAS  Google Scholar 

  9. Liu, Z., Cao, L., He, Y.F., Qiao, L., Xu, C.J., Lu, H.J., Yang, P.Y.: Tandem O-18 stable isotope labeling for quantification of N-glycoproteome. J. Proteome Res. 9, 227–236 (2010)

    Article  CAS  Google Scholar 

  10. Zielinska, D.F., Gnad, F., Wisniewski, J.R., Mann, M.: Precision mapping of an in vivo N-glycoproteome reveals rigid topological and sequence constraints. Cell 141, 897–907 (2010)

    Article  CAS  Google Scholar 

  11. Wright, H.T.: Nonenzymatic deamidation of asparaginyl and glutaminyl residues in proteins. Crit. Rev. Biochem. Mol. Biol. 26, 1–52 (1991)

    Article  CAS  Google Scholar 

  12. Palmisano, G., Melo-Braga, M.N., Engholm-Keller, K., Parker, B.L., Larsen, M.R.: Chemical deamidation: a common pitfall in large-scale N-linked glycoproteomic mass spectrometry-based analyses. J. Proteome Res. 11, 1949–1957 (2012)

    Article  CAS  Google Scholar 

  13. Stavenhagen, K., Hinneburg, H., Thaysen-Andersen, M., Hartmann, L., Silva, D.V., Fuchser, J., Kaspar, S., Rapp, E., Seeberger, P.H., Kolarich, D.: Quantitative mapping of glycoprotein micro-heterogeneity and macro-heterogeneity: an evaluation of mass spectrometry signal strengths using synthetic peptides and glycopeptides. J. Mass Spectrom. 48, 627–639 (2013)

    Article  CAS  Google Scholar 

  14. Zhu, Z., Hua, D., Clark, D.F., Go, E.P., Desaire, H.: GlycoPep detector: a tool for assigning mass spectrometry data of N-linked glycopeptides on the basis of their electron transfer dissociation spectra. Anal. Chem. 85, 5023–5032 (2013)

    Article  CAS  Google Scholar 

  15. Zhu, Z., Su, X., Clark, D.F., Go, E.P., Desaire, H.: Characterizing O-linked glycopeptides by electron transfer dissociation: fragmentation rules and applications in data analysis. Anal. Chem. 85, 8403–8411 (2013)

    Article  CAS  Google Scholar 

  16. Carr, S.A., Huddleston, M.J., Bean, M.F.: Selective identification and differentiation of N-linked and O-linked oligosaccharides in glycoproteins by liquid chromatography-mass spectrometry. Protein Sci. 2, 183–196 (1993)

    Article  CAS  Google Scholar 

  17. Zhou, H., Froehlich, J.W., Briscoe, A.C., Lee, R.S.: The glycofilter: a simple and comprehensive sample preparation platform for proteomics, N-glycomics, and glycosylation site assignment. Mol. Cell. Proteom. 12, 2981–2991 (2013)

    Article  CAS  Google Scholar 

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Acknowledgments

The authors acknowledge funding from the National Institute of Health grant 1R01AI094797.

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Correspondence to Heather Desaire.

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Zhu, Z., Go, E.P. & Desaire, H. Absolute Quantitation of Glycosylation Site Occupancy Using Isotopically Labeled Standards and LC-MS. J. Am. Soc. Mass Spectrom. 25, 1012–1017 (2014). https://doi.org/10.1007/s13361-014-0859-2

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  • DOI: https://doi.org/10.1007/s13361-014-0859-2

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