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O-Glycosylation Ser/Thr GalNAc Ser/Thr Man Ser/Thr Fuc Ser/Thr Glc
Notch Thrombospondin Factor IX Yeast mannoproteins a-dystroglycan Ser/Thr GalNAc Ser/Thr Man Ser/Thr Fuc Ser/Thr Glc Ser/Thr GlcNAc Notch Coagulation Factors Fibrinolytic Factors Nuclear Proteins Cytoplasmic Proteins SEPARATE LECTURE Mucins ALSO: Proteoglycans, Hydroxyproline/Hydroxylysine Glycosylation After Esko, J
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O-Glycosidic Linkage O-glycosidic linkage is sensitive to alkali (regardless of stereochemistry) b-elimination GalNAc GalNAc a a Ser After Esko, J
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Glycan synthesis in a cellular context Most O-Glycosylated
proteins are synthesized in the secretory pathway
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O-Glycosylation Ser/Thr GalNAc Ser/Thr Man Ser/Thr Fuc Ser/Thr Glc
GlcNAc
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Mucin-Type O-GalNAc Glycans
b4 b3 a3 Ser/Thr b6 Major extracellular vertebrate O-glycan Begins in cis-Golgi by attachment of GalNAc in a-linkage to specific Ser/Thr residues Assembly is simpler than N-linked chains - no lipid intermediate is used Always involves nucleotide sugars Always occurs by addition to non-reducing terminus or by branching After Esko, J
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Polypeptide GalNAc Transferases
Regions in white, pink, red, and black represent, respectively, 0–29%, 30–69%, 70–99%, and 100% sequence identity (Hagen et al. (2003) Glycobiology 13:1R-16R). >20 ppGalNAcT family members Share structural features in active site Some have lectin (ricin) domain After Esko, J
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Core 1 and Core 2 Synthesis
T (TF) Antigen Tn Core 2 GlcNAcT Core 1 GalT (cis) Ser/Thr b3 b6 a6 a3 ST6GalNAc1 (trans) Ser/Thr Sialyl Tn Antigen b3 Disialyl T After Esko, J
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From: Tongzhong Ju and Richard D. Cummings
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Core 3 and Core 4 Synthesis
GlcNAcT Core 4 GlcNAcT b3 b3 b6 Ser/Thr Ser/Thr Ser/Thr After Esko, J
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Unusual Core O-Glycan Structures
Ser/Thr b3 Core 4 b6 Core 1 Core 2 Core 7 Ser/Thr a6 Core 6? b6 Core 5 a3 Core 8 After Esko, J
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Mucins are Heavily O-glycosylated
Apomucin contain tandem repeats (8-169 amino acids) rich in proline, threonine, and serine (PTS domains) Glycosylation constitutes as much as 80% of mass and tends to be clustered - bottle brush Expressed by epithelial cells that line the gastrointestinal, respiratory, and genito-urinary tracts After Esko, J
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Mucin Production Lung Epithelium Goblet cells in intestinal crypts
After Esko, J
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Mucins: Protective Barriers for Epithelial Cells
Lubrication for epithelial surfaces Modulate infection: Receptors for bacterial adhesins Secreted mucins can act as decoys Barrier against freezing: Antifreeze glycoproteins [Ala-Ala-Thr]n≤40 with Core 1 disaccharides After Esko, J
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Questions What is the function of multiple polypeptide GalNAc transferases? How is tissue specific expression of transferases regulated? How does competition of transferases for substrates determine the glycoforms expressed by cells and tissues? What roles do chaperones play? After Esko, J
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O-Glycosylation Ser/Thr GalNAc Ser/Thr Man Ser/Thr Fuc Ser/Thr Glc
GlcNAc
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O-Fuc Two Flavors: Mono and Tetrasaccharide
One of the clearest examples of glycosylation (Fringe) modulating signal transduction What other proteins carry O-Fuc and how does glycosylation modulate activity? How is glycosylation regulated?
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O-Glycosylation Ser/Thr GalNAc Ser/Thr Man Ser/Thr Fuc Ser/Thr Glc
GlcNAc
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O-Glc Pathway Shao, L. et al. Glycobiology : ; doi: /glycob/cwf085
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Rumi is OGluT KDEL Retention Signal Temp. Sensitive Mutation
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O-Glc Always a trisaccharide? What enzyme/s for Xyl extension?
Glc & Xyl (except for proteoglycans) rarely used on mammalian glycoproteins--why both here? Does Rumi have both activities? Many of the same proteins as O-Fuc modifed, why? Role in Modulating Signaling? Regulated by enzymes or sugar nucleotide availability?
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O-Glycosylation Ser/Thr GalNAc Ser/Thr Man Ser/Thr Fuc Ser/Thr Glc
GlcNAc
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Alpha-Dystroglycan
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Muscular Dystrophies associated with glycosylation of a - DG
Disease Species Affected Gene Biochemical Lesion Biochemical Phenotype Walker - Warburg Syndrome Human POMT1 O Man addition to Ser/Thr Decreased protein O mannosylation Muscle Eye Brain D isease POMGnT1 Addition of GlcNac b 2 to O Man Underglycosylated a DG, uncapped O Fukuyama type MDC Fukutin Glycosyltransferase like protein DG Limb Girdle and MDC 1C Related Protein l ike Golgi protein Myodystrophy, myd Mouse MDC 1D LARGE like Golgi protein MDC, Congenital Muscular Dystrophy; POMT, Protein Mannosyltransferase; POMGnT1, Protein Mannose, N cetylglucosaminyltransferase 1
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POMT1 in the ER In Complex With POMT2 Uses Dol-Man As Donor
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Figure 3: Glycans linked to Ser/Thr through Man or GalNAc in mammalian brain and muscle. Detected structures on a-DG highlighted by red checks. GnTVb creates b6-branch
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O-Man O-Man is clearly involved in CMD
What mammalian proteins (especially in the brain) are O-Man modified besides a-DG? What are the functions of fukutin and large in O-mannosylation? Why the heterogeneity in O-Man structures, what specific structures at what sites on the protein modulate specific interactions? What is relationship between O-Man and O-GalNAc?
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O-Glycosylation Ser/Thr GalNAc Ser/Thr Man Ser/Thr Fuc Ser/Thr Glc
GlcNAc
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A few more O-glycans…… GalNAc Man Fuc Glc Gal Xyl GlcNAc Ser/Thr
b Ser/Thr Ser/Thr Ser/Thr Ser/Thr Hyl Ser Hyp Ser/Thr O-Xyl….precursor for GAGs… O-GlcNAc….separate lecture—note: recent report of O-GlcNAc on Notch extracellular domain
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O-Glycosylation of Hyl
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O-Glycosylation of Hyl
Found on Collagen and Adiponectin (which has a “collagen-like” domain) Glycosylation Essential for Basement Membrane Formation in Tissues Modulates Collagen Cross-linking? Other proteins with modification?
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The Glycosaminoglycans
After Esko, J
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O-Glycosylation -less studied (until recently?)
-tools to study are underdeveloped -in many cases, clearest functional data (not including folding)
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