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glycogen metabolism. glu cose in body fluids, mainly blood Gl yc og e n - liver. ~. 20 g 190 g. ~. Gl yc ogenol ysi s. ~. 24 hrs starvation. after. Glu coneogenes is. Glucose homeostasis. Carbohydrate/glucose reserve „Buffer role” in the maintenence of blood glucose level.
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glucose in body fluids, mainly blood Glycogen - liver ~ 20 g 190 g ~ Glycogenolysis ~ 24 hrs starvation after Gluconeogenesis Glucose homeostasis Carbohydrate/glucose reserve „Buffer role” in the maintenence of blood glucose level
G-6-P - G-1-P conversion DIPF: diisopropylfuorophosphate - inhibitor
Reaction is pulled in the forward direction by the hydrolysis of PPi
glycogenin • Autocatalytic activity for glycosylation • Human glycogenin gene- 1 muscle, -2 liver • 5 exons • 0.3% of glycogen is protein • Glycogenin content determines the cellular glycogen content
Glycogen branching enzyme: glycosyl (4,6) transferase, -more soluble glycogen -more non reducing terminal residues increased rate of metabolism
Energy balance of glycogenesis for one glycosyl unit G-6-P + ATP + glycogen (n) + H2O Glycogen (n+1) + ADP + 2Pi
Phosphorolysis = cleavage of a bond by Pi Energetically advantageous – released sugar is phosphorylated Glycogen phosphorylase
Debranching enzyme Single polypeptide chain
Glycogenosis = glycogen storagedisease • Targets: liver(blood glucose homeostasis – hypoglycaemia, hepatomegaly) muscle (ATP production, muscle contraction convulsions, weakness, unable for muscle work)
ADP increases during exercise in McArdle disease measured byNMR
Glycogen phosphorylase Muscle dimer or tetramer, Ser 14 phosphorylation/monomer AMP binding site Liver Glucose sensor function Regulated by allosteric interactions and Reversible phosphorylation
Glycogen phosphorylase Pi binding site PLP: pyridoxal phosphate – each catalytic site contains PLP group
PLP - Schiff base linkage at active site of phosphorylase
active usually inactive not phosphorylated phosphorylated
Equilibrium favors Equilibrium favors
Allosteric binding site for nucleotides Transition is controlled by the energy charge of the muscle cell
Glycogen phosphorylase • Phosphorylase a is fully active regardless of the levels of ATP/AMP, G-6-P • Phosphorylase bis usually inactive under physiological circumstances because of the inhibitory effect of ATP and G-6-P
Allosteric binding site for glucose – glucose sensor function – only in liver inactive Under physiological conditions there is no AMP dependent regulation
Activation of phosphorylase kinase e.g. epinephrine δ subunit: calmodulin – calcium sensor
Glycogen synthase • 9 sites for phosphorylation • PKA and other protein kinases can phosphorylate the enzyme • Phosphorylation converts the activea form of the enzyme to inactiveb form
PP1: protein phosphatase 1 • PP1 inactivates phosphorylase kinase and phosphorylase a • PP1 decreases glycogen breakdown • PP1 converts glycogen synthase b to much more active a form • PP1 accelerates glycogen synthesis
PP1: protein phosphatase 1 Rgl: glycogen binding subunit PP1 is active, when associated with glycogen Rgl can be phosphorylated by PKA - causes dissociation from PP1 - inactive
Rgl can be phosphorylated by PKA - causes dissociation from PP1 - inactive Rgl can be phosphorylated by insulin sensitive protein kinase - causes association to PP1 - active
Only in liver Muscle phosphorylase is unaffected by glucose
Regulation of blood glucose level. Hyperglycaemia -1 • Liver increased glucose uptake – GLUT2 Glucokinase – „extra glucose” Increased glycogenesis – insulin; PP1 – glycogen synthase Decreased glycogenolysis – glucose sensor function – glycogen phosphorylase PDH active – increased fatty acid synthesis
Regulation of blood glucose level. Hyperglycaemia -2 • Peripheral tissues pancreas increased glucose uptake – GLUT2 Glucokinase – insulin secretion muscle, adipocytes GLUT4 increased number in membranes Increased glycogenesis Decreased glycogenolysis increased glycolysis – PFK1
Regulation of blood glucose level. Hyperglycaemia -3 Long term effects Decreased amount of PEPCK – decrease in gluconeogenesis