Bioscience Biotechnology and Biochemistry · 2000 · 23 citations · 15 references
Life SciencesBiochemistryBiotechnologyCarbohydrate ChemistryGlycobiologyPlant Molecular BiologyCarbohydrate StructureDevelopmental GlycobiologyGlycan AnalysisGlycan StructureN-linked GlycosylationPlant GlycobiologyDevelopmental Stage StructureGlycan Structural AnalysisGlycan Structure AnalysisHigh-mannose GlycansHigh-mannose N-glycansN-glycan AnalysisN-linked Glycan BiosynthesisSeed Oligosaccharides
Structural changes in N-linked oligosaccharides of glycoproteins during seed development of Ginkgo biloba have been explored to discover possible endogenous substrate(s) for the Ginko endo-beta-N-acetylglucosaminidase (endo-GB; Kimura, Y., et al. (1998) Biosci. Biotechnol. Biochem., 62, 253-261), which should be involved in the production of high-mannose type free N-glycans. The structural analysis of the pyridylaminated oligosaccharides with a 2D sugar chain map, by ESI-MS/MS spectroscopy, showed that all N-glycans expressed on glycoproteins through the developmental stage of the Ginkgo seeds have the xylose-containing type (GlcNAc2 approximately 0Man3Xyl1Fuc1 approximately 0GlcNAc2) but no high-mannose type structure. Man3Xyl1Fuc1GlcNAc2, a typical plant complex type structure especially found in vacuolar glycoproteins, was a dominant structure through the seed development, while the amount of expression of GlcNAc2Man3Xyl1Fuc1GlcNAc2 and GlcNAc1Man3Xyl1Fuc1GlcNAc2 decreased as the seeds developed. The dominantly occurrence of xylose-containing type structures and the absence of the high-mannose type structures on Ginkgo glycoproteins were also shown by lectin-blotting and immunoblotting of SDS-soluble glycoproteins extracted from the developing seeds at various developmental stages. Concerning the endogenous substrates for plant endo-beta-N-acetylglucosaminidase, these results suggested that the endogenous substrates might be the dolicol-oligosaccharide intermediates or some glycopeptides with the high-mannose type N-glycan(s) derived from misfolded glycoproteins in the quality control system for newly synthesized glycoproteins.
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Maturation of the head of bacteriophage T4
Ulrich K. Laemmli, Manuel Favre · Journal of Molecular Biology · 1973 · 3.7K citations
Maturation of the head of bacteriophage T4
Ulrich K. Laemmli, Rodney A. Johnson · Journal of Molecular Biology · 1973 · 1.1K citations
Arnd Sturm, J. Albert van Kuik, J.F.G. Vliegenthart et al. · Journal of Biological Chemistry · 1987 · 163 citations · Full text