Localisation of O-glycans in MUC1 glycoproteins using electron-capture dissociation fragmentation mass spectrometry

Sihlbom C, van Dijk Härd I, Lidell M, Noll T, Hansson G, Bäckström M (2009)
Glycobiology 19(4): 375-381.

Zeitschriftenaufsatz | Veröffentlicht | Englisch
 
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DOI
Autor*in
Sihlbom, C; van Dijk Härd, I; Lidell, M; Noll, ThomasUniBi ; Hansson, G; Bäckström, M
Einrichtung
Technische Fakultät > AG Zellkulturtechnik
Centrum für Biotechnologie > Arbeitsgruppe T. Noll
Centrum für Biotechnologie > Institut für Biochemie und Biotechnik
Abstract / Bemerkung
MUC1 is a mucin glycoprotein containing multiple tandem repeats of 20 amino acids, with five serines and threonines that can be O-glycosylated. Here, we investigated the O-glycosylation site occupancy in MUC1 glycoproteins produced in two mutant CHO cell lines, Lec3.2.8.1 and ldlD. We found that the average site occupancy was higher in MUC1 from Lec3.2.8.1 than from ldlD and that the occupancy increased with the number of tandem repeats in the protein and also depended on the culture conditions used for production. Moreover, we describe the successful use of electron-capture dissociation (ECD) fragmentation, coupled to online liquid chromatography mass spectrometry, to determine the glycosylation of individual sites in recombinant MUC1 proteins with 16 tandem repeats. We analyzed MUC1 tandem repeat peptides with 1-5 GalNAc residues by ECD fragmentation and found that the first site to be glycosylated was either Ser-5 or Thr-6, with the addition of a second GalNAc at Thr-14. For peptides with three GalNAc residues, several different variants of glycopeptides were found, indicating a heterogeneous order of glycosylation at this stage. In contrast, only one variant was found for peptides with four GalNAc residues, where Thr-19 in the PDTR motif was left unglycosylated, indicating that this site is glycosylated last. The results gave novel insight into the order of GalNAc substitution in MUC1 in vivo.
Erscheinungsjahr
2009
Zeitschriftentitel
Glycobiology
Band
19
Ausgabe
4
Seite(n)
375-381
ISSN
0959-6658
eISSN
1460-2423
Page URI
https://pub.uni-bielefeld.de/record/2395445

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Sihlbom C, van Dijk Härd I, Lidell M, Noll T, Hansson G, Bäckström M. Localisation of O-glycans in MUC1 glycoproteins using electron-capture dissociation fragmentation mass spectrometry. Glycobiology. 2009;19(4):375-381.
Sihlbom, C., van Dijk Härd, I., Lidell, M., Noll, T., Hansson, G., & Bäckström, M. (2009). Localisation of O-glycans in MUC1 glycoproteins using electron-capture dissociation fragmentation mass spectrometry. Glycobiology, 19(4), 375-381. https://doi.org/10.1093/glycob/cwn144
Sihlbom, C, van Dijk Härd, I, Lidell, M, Noll, Thomas, Hansson, G, and Bäckström, M. 2009. “Localisation of O-glycans in MUC1 glycoproteins using electron-capture dissociation fragmentation mass spectrometry”. Glycobiology 19 (4): 375-381.
Sihlbom, C., van Dijk Härd, I., Lidell, M., Noll, T., Hansson, G., and Bäckström, M. (2009). Localisation of O-glycans in MUC1 glycoproteins using electron-capture dissociation fragmentation mass spectrometry. Glycobiology 19, 375-381.
Sihlbom, C., et al., 2009. Localisation of O-glycans in MUC1 glycoproteins using electron-capture dissociation fragmentation mass spectrometry. Glycobiology, 19(4), p 375-381.
C. Sihlbom, et al., “Localisation of O-glycans in MUC1 glycoproteins using electron-capture dissociation fragmentation mass spectrometry”, Glycobiology, vol. 19, 2009, pp. 375-381.
Sihlbom, C., van Dijk Härd, I., Lidell, M., Noll, T., Hansson, G., Bäckström, M.: Localisation of O-glycans in MUC1 glycoproteins using electron-capture dissociation fragmentation mass spectrometry. Glycobiology. 19, 375-381 (2009).
Sihlbom, C, van Dijk Härd, I, Lidell, M, Noll, Thomas, Hansson, G, and Bäckström, M. “Localisation of O-glycans in MUC1 glycoproteins using electron-capture dissociation fragmentation mass spectrometry”. Glycobiology 19.4 (2009): 375-381.

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