Structure of glycogen
3 important questions on Structure of glycogen
What is the structure of free glucose and with what can it react?
Glucose has an aldehyde group (reactive group, H-C (delta+) = O (delta-)) which can react with other molecules
- Vitro: Fehlings reagent (Cu2+ ions)
- Cu2+ to 2 Cu
- aldehyde group is oxidized carboxyl group (H-C=O → OH-C=O)
- Vivo: amino group of protein
- glucose can attache to proteins in 2 ways
- Glycosylation: glucose transfer via condensation reaction (enzymatic)
- Glycation: spontanous irreversible transfer of glucose (non-enzamatic)
- Intramolecular: The C5 hydroxyl group
- glucose react with hydroxyl group at C5, forming a alfa-anomer (axial) or beta-anomer (equatorial)
- possition of OH group changes
What is a glucan?
- has 2 ends, reducing end (OH) = squiggle
- glycosidic bonds (covalent)
- alfa-(1,4)-glycosidic bonds: between glucose residues
- alfa-(1,6)-glycosidic bonds: branch points
What is proteo-glycogen? How is it formed?
Initiation
- Glycogenin (GN) has a Tyr residue when a homodimer forms, it can auto-glycosylate and continues until 8 glucose are added
Elongation
- Glycogen synthase (GS) extends existing chains
Branching
- Branching enzyme (BE) removes an oligosaccharide of 7 glucose residues from the non reducing end that is minimally 11 glucose residues in length
- transfers it to create a new branch point that is at least 4 glucose residues away from a preexisting branch point
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