Glycobiology · 2001 · 49 citations · 26 references
Life SciencesBiochemistryMolecular BiologyEnzymologyGlycobiologyParasite ImmunologyGlycan AnalysisGlycan BiosynthesisGlycan StructureGlycoproteomicsGlycosylation PathwaysN-linked GlycosylationChemical DerivatizationDerivatizationDigestionEnzymatic DigestionExoglycosidase ActivityFucosylation PatternsN-glycan Core FucosylationOxidation
The glycobiology of Schistosoma mansoni is dominated by developmentally regulated expression of various fucosylated structures, most notably the Lewis X epitope and a multifucosylated sequence, Fuc alpha1-->2Fuc alpha1-->, in its various forms. For the infective cercarial stage, Lewis X has been structurally identified on glycosphingolipids and N-glycans of total glycoprotein extracts, and a population of multifucosylated glycoproteins were found to carry a unique terminal sequence, +/-Fuc alpha1-->2Fuc alpha1-->[3GalNAc beta1-->4(Fuc alpha1-->2Fuc alpha1--> 2Fuc alpha1-->3) GlcNAc beta1-->3Gal alpha1-->](n), on their O-glycans. Using a mass spectrometry approach coupled with chromatographic separation, sequential exoglycosidase digestion, periodate oxidation, and other chemical derivatization, we demonstrate that Lewis X could also be carried on the cercarial O-glycans, but the two distinctive sets of fucosylated epitopes were conjugated to two different core structures. Lewis X, lacNAc, or single GlcNAc was found to attach directly to the -->3Gal beta1-->3GalNAc core and indirectly via another beta-Gal residue branching off from C6 of the reducing end GalNAc to give a biantennary-like structure. The -->3(+/-Gal beta1-->6)Gal beta1-->3(-->3Gal beta1-->6)GalNAc core thus characterized represents a novel core type for O-glycans. In contrast, the previously characterized multifucosylated terminal sequences were carried on conventional type 1 and 2 cores. The smallest structures of the reductively released O-glycans were defined as GalNAc beta1-->4GlcNAc beta1-->3Gal beta1-->3GalNAcitol with a total of two to four fucoses attached to the terminal lacdiNAc. alpha-Galactosylation of the nonreducing terminal beta-GalNAc instead of fucose capping leads to further elongation with another lacdiNAc unit that could also extend directly from C6 of the reducing end GalNAc and similarly elongated or terminated.
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Alexandra van Remoortere, Cornelis H. Hokke, Govert J. van Dam et al. · Glycobiology · 2000 · 134 citations · Full text
Govert J. van Dam, Aldert A. Bergwerff, Jane Thomas‐Oates et al. · European Journal of Biochemistry · 1994 · 132 citations · Full text
Kay‐Hooi Khoo, Delphi Chatterjee, J P Caulfield et al. · Glycobiology · 1997 · 127 citations · Full text
Kay‐Hooi Khoo, Sunil Sarda, Xiaofei Xu et al. · Journal of Biological Chemistry · 1995 · 127 citations · Full text