Glycoproteins and Mucins B.Sopko
Content Glycoproteins: Structures and Linkages Interconversions and activation of dietary sugars Other pathways of sugar nucleotide metabolism Biosynthesis of oligosaccharides Functions of the oligosaccharide chains of glycoproteins Mucins Pathological glycosylation
Glycoproteins: Structures and Linkages Glycoproteins and Proteoglycans Glycoproteins Proteoglycans Protein >> carbohydrate Proteins conjugated to saccharides lacking a serial repeat unit Carbohydrate >> protein Repeat unit HexN and HexUA Glycosaminoglycans and Mucopolysaccharides
Glycoproteins: Structures and Linkages Structures of the oligosaccharides attached to proteins
Glycoproteins: Structures and Linkages Structures of the oligosaccharides attached to proteins
Interconversions and activation of dietary sugars
Fructose metabolism
UDP-glucose
GDP-mannose
Synthesis of amino-sugars and sialic acids
Interconversions and activation of dietary sugars - overview
Biosynthesis of oligosaccharides N-linked glycoproteins
N-linked glycoproteins
Serine O-linked glycoproteins
Route from the Golgi complex to the final destination
Functions of the oligosaccharide chains of glycoproteins N-linked oligosaccharides have an important role in protein folding High-mannose oligosaccharides target some proteins to specific sites in the cell The oligosaccharide chains of glycoproteins increase the solubility and stability of proteins Both N- and O-linked glycan structures are involved in recognition processes
High-mannose oligosaccharides target some proteins to specific sites in the cell
N-linked oligosaccharides have an important role in protein folding
The oligosaccharide chains of glycoproteins increase the solubility and stability of proteins
Both N- and O-linked glycan structures are involved in recognition processes
Lectins Lectins are defined as proteins that do not have enzymatic activity but that reversibly bind monosaccharides and oligosaccharides with high specificity.
Mucins - characterization Complex glycoproteins synthetized in epithelial cells Components of mucus secretions covering epithelial cells in gastrointestinal, urogenital, tracheobronchial, ocular and auditory systems of all vertebrates (but they can be found in all eukaryotes) Very rich in carbohydrates (50-90% of mucin mass is composed by sugars) and saccharides are linked to protein via O-glycosidic bond O-glycans are linked to serine/threonine in specific domain called tandem repeat Some mucins can also contain N-glycosidic oligosaccharides, but they are bound only in cysteine-rich domain Marked MUC1.
Mucins - structure
Mucins - types Membrane-tethered with TR (membrane mucins) e.g. MUC1, MUC4 Secreted, cysteine-poor with TR (gel forming cystein-poor mucins) - e.g. MUC7 Secreted, cysteine-rich with TR - MUC2, MUC5AC Mucins without TR
Mucins synthesis
Secreted mucins in the airways mucus gel and their sites of synthesis.
Secreted mucins in the airways mucus gel and their structure
Pathological glycosylation and glycation
I-CELL DISEASE I-cell disease results from an enzyme deficiency so that lysosomal enzymes do not aquire the targeting signal, mannose 6-phosphate. Fibroblasts in this disease have dense inclusion bodies (I-cells) and are deficient in many lysosomal enzymes. The lysosomes become engorged with indigestible substrates, leading to death in infancy.
N-linked oligosaccharides have an important role in protein folding
Carbohydratedeficient glycoprotein syndromes (CDGSs)
Carbohydrate-deficient glycoprotein syndromes (CDGSs) Disease Enzyme Deficiency Symptoms/Comments Aspartylglucosaminuria β-mannosidosis α-mannosidosis G M1 Gangliosidosis Sandhoff disease Sialidosis (also identified as Mucolipidosis I) aspartylglucosaminidase (N-aspartyl-β-glucosaminidase) β-mannosidase α-mannosidase β-galactosidase β-hexosaminidases A and B neuraminidase (sialidase) progressive mental retardation, delayed speech and motor development, coarse facial features primarily neurological defects, speech impairment mental retardation, dystosis multiplex, hepatosplenomegaly, hearing loss, delayed speech also identified as a glycosphingolipid storage disease or lysosomal storage disease also identified as a glycosphingolipid storage disease or lysosomal storage disease myoclonus, congenital ascites, hepatosplenomegaly, coarse facial features, delayed mental and motor development Fucosidosis α-fucosidase progressive motor and mental deterioration, growth retardation, coarse facial features, recurrent sinus and pulmonary infections
Decreased Cl - concentration results in thicker and less fluid mucous secretion Cystic fibrosis
Glycation (spontaneus glycosylation)
Glycation (spontaneus glycosylation) Extracellular proteins Intracellular proteins Long-lived proteins Collagen Type I, III and IV, cartilage, elastin, myelin, proteoglycan Lens crystallins, Neurofilaments Short-lived proteins Plasma proteins such as Apo B, LDL, albumin, immunoglobulins Hemoglobin, enzymes, lysosomes, ribonuclease and several membrane proteins
Glycation (spontaneus glycosylation)