2. GLYCOGEN METABOLISM
Carl Cori and Gerty -glycogen degradation.
Glycogen synthesis, Luis Leloir (Argentina) was
awarded Nobel prize in 1970.
Earl Sutherland studied the role of cyclic AMP as
the second messenger in glycogenolysis.
Glycogen is a homopolysaccharide with glucose
units linked in alpha-1, 4 linkages (straight line) and
alpha-1, 6 linkages (branching point).
Branching makes the molecule more globular and
less space-consuming.
7. FIG. Control of glycogen phosphorylase in muscle. The sequence of reactions arranged as a
cascade allows amplification of the hormonal signal at each step. n, number of glucose residue
8.
9.
10. Fig . Coordinated control of glycogenolysis and
glycogenesis by cAMP dependent protein kinase.
Coordinated control of glycogenolysis and glycogenesis by
cAMP-dependent protein kinase.
The reactions that lead to glycogenolysis as a result of an
increase in cAMP concentrations are shown with bold
arrows.
Inhibited by activation of protein phosphatase-1 are shown
with dashed arrows.
The reverse occurs when cAMP concentrations decrease as
a result of phosphodiesterase activity, leading to
glycogenesis.
11. Functions of Glycogen
1. storage form , liver and
muscle.
liver glycogen is to provide glucose during fasting.
The glycogen content of liver (10 g/100 g tissue)
skeletal muscle (1–2 g/100 g)
2. liver glycogen is broken down and helps to
maintain blood glucose level.
After taking food, blood sugar tends to rise,
12. Functions of Glycogen continue…
After taking food, blood sugar tends to rise, which
causes glycogen deposition in liver.
About 5 hours after taking food, the blood sugar tends
to fall.
But, glycogen is lyzed to glucose so that the energy
needs are met.
After about 18 hours fasting, most of the liver glycogen
is depleted, when depot fats are hydrolyzed and energy
requirement is met by fatty acid oxidation .
3. The function of muscle glycogen is to act as reserve
fuel for muscle contraction.
4. All the enzymes related to glycogen metabolism are
cytoplasmic.
15. Step 1 -Glycogen Phosphorylase
i. Glycogen phosphorylase removes glucose as glucose- 1-
phosphate from glycogen (phosphorolysis) .
It contains pyridoxal phosphate (PLP) as a prosthetic
group. The alpha-1, 4 linkages in the glycogen are cleaved.
ii. It removes glucose units one at a time. Enzyme
sequentially hydrolyzes alpha-1, 4 glycosidic linkages,
16.
17. Step 2.Debranching by Bifunctional (Two) Enzymes
i. A block of 3 glucose residues (trisaccharide unit) are
transferred from the branching point to another branch.
Enzyme is alpha-1, 4 → alpha-1, 4 glucan transferase.
ii. Now the branch point is free.
Then alpha-1, 6- glucosidase (debranching enzyme) can
hydrolyze the remaining glucose unit held in alpha-1, 6
linkage at the branch point .
iii. This glucose residue is released as free glucose ,the ratio of
glucose-1-phosphate to free glucose is about 8:1.
iv. The transferase and alpha-1, 6-glucosidase will together
convert the branch point to a linear one.
With the removal of the branch point, phosphorylase nzyme
can proceed with its action.
18.
19. Sep 3. Phosphoglucomutase
Phosphorylase reaction produces glucose-1-
phosphatem while debranching enzyme releases
glucose.
The glucose- 1-phosphate is converted to glucose-6-
phosphate by phosphoglucomutase .
20. Step 4.Glucose-6-phosphatase in Liver
Next, hepatic glucose-6-phosphatase hydrolyzes
glucose- 6-phosphate to glucose.
The free glucose is released to the bloodstream.
21. Muscle lacks Glucose -6-phosphatase
Muscle will not release glucose to the
bloodstream, because muscle tissue does not
contain the glucose-6-phosphatase.
Instead, in muscle, glucose-6-phosphate
undergoes glycolysis to produce ATP for muscle
contraction.
22. Energetics Glycogenolysis
i. The energy yield from one glucose residue derived
from glycogen is 3 ATP molecules, because no ATP is
required for initial phosphorylation of glucose (step
1 of glycolysis).
ii. If glycolysis starts from free glucose only 2 ATPs are
produced.
24. GLYCOGEN SYNTHESIS (GLYCOGENESIS)
The glycogen synthesis occurs by a pathway
distinctly different from the reversal of glycogen
breakdown, which would prevent the operation of
futile cycles.
The steps are:
25. Step-1. Activation of Glucose
UDP glucose is formed from glucose-1-phosphate
and UTP (uridine triphosphate) by the enzyme UDP-
glucose pyrophosphorylase.
26.
27. Step- 2.Glycogen Synthase
The glucose moiety from UDP-glucose is transferred
to a glycogen primer (glycogenin) molecule.
The primer is essential to accept the glycosyl unit.
The primer is made up of a protein-carbohydrate
complex.
It is a dimeric protein, having two identical
monomers.
An oligosaccharide chain of 7 glucose units is added
to each monomer.
28.
29. Step- 2.Glycogen Synthase continue….
In the next step, activated glucose units are
sequentially added by the enzyme glycogen
synthase .
The glucose unit is added to the nonreducing
(outer) end of the glycogen primer to form an
alpha-1, 4 glycosidic linkage and UDP is liberated.
30.
31. Glycogen Synthase and Primer
The glycogen primer is formed by autoglycosylation
of glycogenin.
Glycogenin is a dimeric protein, the monomers
glycosylating each other using UDP glucose till
seven glucose units are added.
This molecule acts as the glycogen primer to which
glucose units are added by glycogen synthase.
32. Step-3.Branching Enzyme
i. The glycogen synthase can add glucose units only in
alpha-1, 4 linkage.
A branching enzyme is needed to create the alpha-1,
6 linkages.
ii. When the chain is lengthened to 11–12 glucose
residues, the branching enzyme will transfer a block of
6 to 8 glucose residues from this chain to another site
on the growing molecule.
The enzyme amylo- [1, 4]→[1, 6]-transglucosidase
(branching enzyme) forms this alpha-1, 6 linkage.
iii. To this newly created branch, further glucose units can
be added in alpha-1, 4 linkage by glycogen synthase.
33. Regulation of Glycogen Metabolism
i. The synthesis and degradation pathways are reciprocally regulated
to prevent futile cycles.
ii. The phosphorylated form of glycogen phosphorylase is active;
but glycogen synthase becomes inactive on phosphorylation.
The covalently modified phosphorylase is active even without
AMP.
Active (dephosphorylated) glycogen synthase is responsive to the
action of glucose-6- phosphate.
Covalent modification modulates the effect of allosteric regulators.
The hormonal control by covalent modification and allosteric
regulation are
interrelated.
iii. These hormones act through a second messenger, cyclic AMP
(cAMP)
iv. The covalent modification of glycogen phosphorylase
and synthase is by a cyclic AMP mediated
34. Regulation of Glycogen Metabolism
iv. The covalent modification of glycogen
phosphorylase and synthase is by a cyclic AMP
mediated cascade.
Specific protein kinases bring about
phosphorylation and protein phosphatases cause
dephosphorylation.
35. Regulation of Glycogen Metabolism
Generation of Cyclic AMP (cAMP)
Protein Kinase Activation
Phosphorylase Kinase Activation
Glycogen Phosphorylase in Liver and Muscle
Glycogen Synthase
36.
37.
38.
39. Generation of Cyclic AMP (cAMP)
i. Both liver and muscle phosphorylases are activated by
a cyclic AMP mediated activation cascade triggered
by the hormonal signal.
ii. The hormones epinephrine and glucagon can
activate liver glycogen phosphorylase but glucagon
has no effect on the muscle.
iii. When the hormone binds to a specific receptor on
the plasma membrane, the enzyme adenyl cyclase is
activated which converts ATP to cyclic AMP (cAMP).
iv. When level of cyclic AMP rises, it will activate a
protein kinase .
40. Protein Kinase Activation
The protein kinase is inactive when the catalytic (C)
and regulatory (R) subunits are associated with
each other.
Earl Sutherland studied the role of cyclic AMP as the
second messenger in glycogenolysis.
The cAMP combines with the R subunit so that the
C subunit is free to have its catalytic activity.
PKA is an enzyme that can phosphorylate serine
and threonine residues of several enzyme proteins
and is activated by cAMP which combines with the
regulatory subunit of PKA.
In the absence of cAMP, PKA is an inactive tetramer.
42. Protein Kinase Activation
The intracellular concentration of cAMP therefore
decides the level of active PKA.
cAMP level depends on the activity of adenylate
cyclase and phosphodiesterase.
Cyclic AMP level is increased by glucagon and
decreased by insulin.
43.
44. Phosphorylase Kinase Activation
The active protein kinase can now convert the phosphorylase
kinase to an active phosphorylated form, which converts
phosphorylase-b to phosphorylase-a .
Phosphorylase kinase itself is a tetrameric enzyme (alpha,
beta, gamma, delta).
The gamma subunit has the catalytic site and the other 3
subunits have regulatory effects.
Phosphorylase kinase is activated by Ca++ and
phosphorylation of alpha and beta subunits by PKA.
Phosphorylation of alpha and beta subunits relieves
autoinhibition of catalytic activity of gamma subunit.
Binding of Ca++ to the delta subunit which is identical to
calmodulin (CaM) is also necessary for full activity of delta
subunit. since it also has a role in dysregulating the
45. Phosphorylase Kinase Activation continue..
It also has a role in dysregulating the gamma
subunit.
Calcium triggers muscle contraction as well as
glycogen breakdown through the action of
phosphorylase kinase.
The rate of glycogenolysis is linked to rate of
muscle contraction.
46.
47. Phosphorylase Kinase Activation continue..
The dephosphorylation of the active form by protein
phosphatase 1 (PP1) involves removal of phosphate group
from phosphorylase a and alpha and beta subunits of
phosphorylase kinase.
The activity of PP1 is controlled differently in liver and
muscle.
The catalytic subunit of PP1 in muscle is active only when it is
bound to glycogen through the glycogen binding GM subunit.
The phosphorylation of PP1 by an insulin stimulated protein
kinase (site1) activates the enzyme where as phosphorylation
at site 2 by PKA makes its action ineffective.
When cAMP level is high, PP1 is inhibited by inhibitor1 which
is activated by phosphorylation by PKA.
The effect of cyclic AMP is not only by increasing the
phosphorylation of enzymes, but also by decreasing
dephosphorylation.
48. Glycogen Phosphorylase in Liver
a. Liver: The liver phosphorylase-b is the inactive form.
It becomes active on phosphorylation.
The active enzyme is denoted as phosphorylase-a.
The enzyme is inhibited by ATP and glucose-6-phosphate.
In the liver the PP1 is regulated differently through the
intermediary of glycogen binding subunit (GL).
GL complex can bind to R and T forms of phosphorylase a.
The phosphate group attached to ser14 is exposed only in
the T state, so that PP1 can convert phosphorylase a to
phosphorylase b.
Glucose is an allosteric inhibitor of phosphorylase a.
Insulin favors this effect by promoting the uptake and
phosphorylation of glucose.
49. Glycogen Phosphorylase in Muscle
b. Muscle: Skeletal muscle glycogen is degraded only when the
demand for ATP is high.
The regulation of glycogenolysis in skeletal muscle is by
epinephrine.
Glucagon has no effect on muscle glycogenolysis.
AMP formed by degradation of ATP during muscle contraction
is an allosteric activator of phosphorylase b.
The active form of phosphorylase is referred to as ‘a’ (active,
phosphorylated) and the relatively inactive dephosphorylated
form as ‘b’.
The active glycogen synthase (a) is dephosphorylated and
phosphorylated (b) is relatively inactive.
Glycogen phosphorylase is activated by phosphorylation by
phosphorylase kinase that adds phosphate group to a specific
serine residue of phosphorylase b (ser14).
This phosphorylase kinase, in
50. FIG. Control of glycogen phosphorylase in muscle. The sequence of reactions arranged as a
cascade allows amplification of the hormonal signal at each step. n, number of glucose residue
51. Glycogen Phosphorylase in Muscle
This phosphorylase kinase, in turn, is activated by
protein kinase A or cyclic AMP dependent protein
kinase.
Phosphoprotein phosphatase I dephosphorylates
both phosphorylase kinase and phosphorylase b.
Phosphorylase b is sensitive to allosteric effectors
like AMP but phosphorylase a is not sensitive.
High concentration of ATP and glucose-6-phosphate
in the cell will inhibit phosphorylase b.
52. Glycogen Synthase
i. Glycogen synthase and phosphorylase activities are
reciprocally regulated .
ii. The same protein kinase, which phosphorylates the
phosphorylase kinase would also phosphorylate glycogen
synthase.
iii. The activity of the glycogen synthase is markedly decreased
on phosphorylation.
Insulin promotes glycogen synthesis by favouring
dephosphorylation.
Glycogen synthase is active in the dephosphorylated state.
Phosphorylase kinase can phosphorylate glycogen synthase
and inactivate the enzyme.
PKA can also inactivate the enzyme by phosphorylation.
Ca++ and calcium dependent cam kinase also phosphorylate
the enzyme.
53.
54.
55. Glycogen Synthase continue….
Relative rates of glycogen synthesis and breakdown are
controlled by the action of PKA, phosphorylase kinase
and PP1.
PP1 can activate glycogen synthase only after
dephosphorylating and inactivating phosphorylase a.
The regulation of glycogen phosphorylase and synthase
is a typical example of multisite phosphorylation
(primary and secondary sites) for metabolic regulation.
Control by allosteric effectors is superimposed on
covalent modification.
Glucose-6-phosphate can activate glycogen synthesis.
Insulin activates PP1 and PDE which decreases cAMP
level and increases G6P level to promote glycogen
synthesis.
56. Glycogen Synthase continue….
The reciprocal regulation of glycogenolysis and
glycogenesis is by covalent modification
(phosphorylation and dephosphorylation).
Insulin and glucagon are the major regulatory
hormones, although epinephrine has stimulatory
effect on glycogenolysis in both liver and muscle.
They bring about alterations in the activity of
protein kinases and phosphatases by varying the
level of cAMP.
57. Summary of Glycogen Regulation
i. The key enzyme for glycogenolysis is phosphorylase, which
is activated by glucagon and epinephrine, under the
stimulus of hypoglycemia.
ii. The key enzyme for glycogen synthesis is glycogen
synthase, the activity of which is decreased by glucagon
and epinephrine but is enhanced by insulin, under the
stimulus of hyperglycemia .
Glycogen metabolism is regulated by coordinated
regulation of glycogen synthase and
glycogenphosphorylase.
The regulatory mechanisms include:
Allosteric control as well as hormonal control by covalent
modification of enzymes.
The allosteric effectors are ATP, glucose-6-phosphate and
AMP.
64. Glycogen Storage Disease Type-I
1. It is also called Von Gierke’s Disease.
Most common type of glycogen storage disease is type I.
2. Incidence is 1 in 100,000 live births.
3. Glucose-6-phosphatase is deficient.
4. Fasting hypoglycemia that does not respond to stimulation by adrenaline.
The glucose cannot be released from liver during over night fasting 5.
Hyperlipidemia, lactic acidosis and ketosis.
6. Glucose-6-phosphate is accumulated, so it is channeled to HMP shunt
pathway producing more ribose and more purine nucleotides.
7. Purines are then catabolized to uric acid, leading to hyperuricemia.
8. Glycogen gets deposited in liver.
Massive liver enlargement may lead to cirrhosis.
9. Children usually die in early childhood.
10. Treatment is to give small quantity of food at frequent intervals.
Other types : 1 in 1 million births
65. Pompe’s disease
• infantile-onset Pompe’s disease Myozyme
(recombinant human acid alpha glucosidase,
rhGAA) is administered intravenously.