Asn-linked oligosaccharide chain of a crenarchaeon, Pyrobaculum calidifontis, is reminiscent of the eukaryotic high-mannose-type glycan
- PMID: 28510654
- DOI: 10.1093/glycob/cwx044
Asn-linked oligosaccharide chain of a crenarchaeon, Pyrobaculum calidifontis, is reminiscent of the eukaryotic high-mannose-type glycan
Abstract
Pyrobaculum calidifontis is a hyperthermophilic archaeon that belongs to the phylum Crenarchaeota. In contrast to the phylum Euryarchaeota, only the N-glycan structure of the genus Sulfolobus is known in Crenarchaeota. Here, we enriched glycoproteins from cultured P. calidifontis cells, by ConA lectin chromatography. The MASCOT search identified proteins with at least one potential N-glycosylation site. The tandem mass spectrometry (MS/MS) analysis of 12 small tryptic glycopeptides confirmed the canonical N-glycosylation consensus in P. calidifontis. We determined the N-linked oligosaccharide structure produced by an in vitro enzymatic oligosaccharyl transfer reaction. Pyrobaculum calidifontis cells were cultured in rich medium supplemented with 13C-glucose, for the metabolic labeling of N-oligosaccharide donors. An incubation with a synthetic peptide substrate produced glycopeptides with isotopically labeled oligosaccharide moieties. The MS and nuclear magnetic resonance analyses revealed that the P. calidifontisN-glycan has a biantennary, high-mannose-type structure consisting of up to 11 monosaccharide residues. The base portion of the P. calidifontisN-glycan strongly resembles the eukaryotic core structure, α-Man-(1-3)-(α-Man-(1-6)-)β-Man-(1-4)-β-GlcNAc-(1-4)-β-GlcNAc-Asn. Structural differences exist in the anomeric configuration between Man and GlcNAc, and the chitobiose structure is chemically modified: one GlcNAc residue is oxidized to glucoronate, and the GlcNAc residues are both modified with an additional acetamido group at the C-3 position. As a result, the core structure of the P. calidifontisN-glycan is α-Man-(1-3)-(α-Man-(1-6)-)α-Man-(1-4)-β-GlcANAc3NAc-(1-4)-β-GlcNAc3NAc-Asn, in which the unique features of the P. calidifontisN-glycan are underlined. In spite of these differences, the structure of the P. calidifontisN-glycan is the most similar to the eukaryotic counterparts, among all archaeal N-glycans reported to date.
Keywords: N-oligosaccharide structure; Pyrobaculum calidifontis; Creanarchaeota; glycoproteins; metabolic labeling of N-oligosaccharide donor.
© The Author 2017. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.
Similar articles
-
Comparative Analysis of Archaeal Lipid-linked Oligosaccharides That Serve as Oligosaccharide Donors for Asn Glycosylation.J Biol Chem. 2016 May 20;291(21):11042-54. doi: 10.1074/jbc.M115.713156. Epub 2016 Mar 25. J Biol Chem. 2016. PMID: 27015803 Free PMC article.
-
Site-specific glycosylation analysis of the bovine lysosomal alpha-mannosidase.Glycobiology. 2006 May;16(5):440-61. doi: 10.1093/glycob/cwj081. Epub 2006 Jan 31. Glycobiology. 2006. PMID: 16449350
-
Transglycosylation of intact sialo complex-type oligosaccharides to the N-acetylglucosamine moieties of glycopeptides by Mucor hiemalis endo-beta-N-acetylglucosaminidase.Carbohydr Res. 1996 Oct 4;292:61-70. doi: 10.1016/s0008-6215(96)91025-3. Carbohydr Res. 1996. PMID: 8870237
-
Methods in enzymology: O-glycosylation of proteins.Methods Enzymol. 2005;405:139-71. doi: 10.1016/S0076-6879(05)05007-X. Methods Enzymol. 2005. PMID: 16413314 Review.
-
Synthetic and semi-synthetic approaches to unprotected N-glycan oxazolines.Beilstein J Org Chem. 2018 Feb 15;14:416-429. doi: 10.3762/bjoc.14.30. eCollection 2018. Beilstein J Org Chem. 2018. PMID: 29520306 Free PMC article. Review.
Cited by
-
A Radioisotope-free Oligosaccharyltransferase Assay Method.Bio Protoc. 2019 Mar 5;9(5):e3186. doi: 10.21769/BioProtoc.3186. eCollection 2019 Mar 5. Bio Protoc. 2019. PMID: 33654988 Free PMC article.
-
N-glycosylation in Archaea - Expanding the process, components and roles of a universal post-translational modification.BBA Adv. 2024 Aug 29;6:100120. doi: 10.1016/j.bbadva.2024.100120. eCollection 2024. BBA Adv. 2024. PMID: 39296579 Free PMC article.
-
Agl24 is an ancient archaeal homolog of the eukaryotic N-glycan chitobiose synthesis enzymes.Elife. 2022 Apr 8;11:e67448. doi: 10.7554/eLife.67448. Elife. 2022. PMID: 35394422 Free PMC article.
-
Structural Insight into the Mechanism of N-Linked Glycosylation by Oligosaccharyltransferase.Biomolecules. 2020 Apr 17;10(4):624. doi: 10.3390/biom10040624. Biomolecules. 2020. PMID: 32316603 Free PMC article. Review.
-
Characterization of protein glycosylation in an Asgard archaeon.BBA Adv. 2024 Jul 11;6:100118. doi: 10.1016/j.bbadva.2024.100118. eCollection 2024. BBA Adv. 2024. PMID: 39081798 Free PMC article.
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials
Miscellaneous
