Glycogen metabolism Flashcards

1
Q

glycogen is made from what form of glucose

A

alpha-D-glucose

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2
Q

the primary bond

A

alpha-1,4-glycosidic linkage

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3
Q

the branch bond

A

alpha-1,6-glycosidic linkage

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4
Q

glycogen is store in…as…

A

cytoplasm of the liver and muscle (primarily) as large hydrated granules

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5
Q

function of liver vs muscle glycogen

A

liver - maintain blood glucose concentration

muscle - contraction

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6
Q

blood glucose can be obtained from what sources?

A

diet - sporadic
degradation of glycogen - less than 24 hr supply
gluconeogenesis - slow

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7
Q

function of muscle glycogen

A

fuel reserve for synthesis of ATP to power mm contraction
glucose can not leave cell because it remains phosphorylated
mm lacks; glucose-6-phosphatase

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8
Q

important enzyme in the liver

A

glucose-6-phosphatase

“frees” glucose so that it can leave cell and enter blood

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9
Q

special enzymes of glycogenesis

A
  1. glycogen synthase
    - requires a primer (glycogen or glycogenin protein)
  2. branching enzyme
    - breaks alpha 1,4 -> transfer to alpha 1,6

(first glucose must become activated = UDP-Glucose)

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10
Q

what must happen to glucose before it can be used in glycogenesis?

A

must be activated w a nucleotide sugar

uridylyltransferase / UDPFle pyrophosphorylase

UTP + Glucose-1-P -> UDP-Glucose + PPi

note the subsequent hydrolysis of PPi by Pyrophosphatase makes this rxn favorable

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11
Q

what enzyme is equivalent to glucokinase but acts in the reverse direction?

A

glucokinase = in liver, phosphorylates glc -> G-6-P

glucose-6-phosphatase (liver only) removes that P group

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12
Q

significance of alpha-D-glucose attached to uridine diphosphate (UDP)

A

the soucre of all the glucosyl residues added to the growing glycogen molecule

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13
Q

why can’t free glucose accept a mol of glucose from UDP-glucose to initiate chain synthesis?

A

the smaller the glycogen the larger the Km of the synthase, so at its physiologic conc glucose can’t serve as a primer for glycogen synthesis
glycogen frament can serve as a primer

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14
Q

what is glycogenin? what does it do?

A

protein that acts as a primer via autoglucosylation
OH grp of Tyr-194 accepts initial glucosyl unit
both enzyme and substrate
after ~ 7 residues glycogen synthase takes over

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15
Q

does glycogen synthase require ATP?

A

no - a synthetase normally would

a synthase - catalyzes a synthetic rxn in which two units are joined wo the direct participation of ATP

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16
Q

glycogen synthase, what does it do?

A

transfers glucose from UDP-glc to the non-reducing end of the growing chain

Rate limiting and Regulated step
a homotetramer

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17
Q

branching enzyme

A

glucosyl 4:6 transferase

clease an alpha-1,4 bond, transfers chain (6-8residues) to another residue on chain and forms a alpha-1,6-bond

results in two nonreducing ends that can be added to by glycogen synthase

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18
Q

why branching?

A

increased solubility

increased number of nonreducing ends to which new glycosyl residues can be added

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19
Q

what limits glycogen synthesis?

A

feedback control by glycogen

not well understood

20
Q

glycogen phosphorylase

A

first step in glycogen degradation
uses Pi to cleave the alpha-1,4- bonds -> G-1-P + remaining glycogen
stops 4 residues from branch pt => limit dextrin

alpha-1,4-glucosidase, phosphorlysis, rate-limiting
requires: PLP pyridoxal phosphate (B6)

21
Q

phosphoglucomutase

A

coverts G-1-P -> G-6-P

22
Q

debranching enzyme

A

second step in glycogen
bifunctional enzyme:
1. 4-alpha-D-glucantransferase
transfers 3 outer residues of the limit dextrin to a nonreducing end, leaving only 1 glucosyl residue in an alpha-1,6-linkage

  1. amylo-alpha-1,6 glucosidase
    cleaves the 1 remaining residue
    => free glucose! (not phosphorylated)
23
Q

lysosomal glycogen degradation pathway

A

quantitatively less significant
1-3% glucogen degraded in lysosom by the acid hydrolase:
alpha-glucosidase

24
Q

forms that glycogen phosphorylase exists in, what enzyme(s) cause these changes?

A

Glycogen Phosphorylase
a = active form: Phosphorylated (phosphorylase kinase)
b= inactive form: de-phosphorylated (phosphorylase phosphatase)

25
Q

how is Phosphorylase Kinase activated? what does it do?

A

Phosphorylase Kinase
activated by Protein Kinase A
a = active form is Phosphorylated

phosphorylase kinase can now phosphorylate (activate) glycogen phosphorylase (glycogenolysis)

26
Q

how is phosphorylase kinase inactivated?

A

phosphoprotein phosphatase removes Pi thus inactivating posphorylase kinase

27
Q

summarize the activation of Glycogen Phosphorylase (glycogenolysis)

A
hormone signal (glucagon, epinephrine)
increase cAMP
activation of Protein Kinase A
Phosphorylase kinase (active -P'ated)
Glycogen phosphorylase (active - P'ated)
28
Q

hormone signals that initiate glycogenolysis and where?

what processes do they inhibit?

A

Both activate Protein Kinase A

Glucagon;

  • pancreatic alpha cells
  • LIVER

Epinephrine:

  • adrenal medulla, synth from tyr, stress
  • binds beta-adrenergic receptors
  • Liver & Muscle

both Inhibit: conversion of UDP-Glucose -> glycogen & G-6-P -> Pyruvate (aka storage)

29
Q

forms of Glycogen Synthase, enzymes that act on it

A
a = active; DePhosphorylated - several Kinases (opp of glycogenolysis - Glucogen Phosphorylase)
b = inactive, Phosphorylated form - Phosphoprotein Phosphatase
30
Q

how does cAMP regulate glycogen metabolism?

A

simultaneously
activates glycogenolysis
inhibits glycogenesis
all this via protein phosphorylation by cAMP-dependent PKA

31
Q

protein phosphatase inhibitor

A

this is also phosphorylated and thus activated by PKA along with glycogen phosphorylase kinase (activates glycogen phosphorylase)

this prevents the dephosphorylation (inactivation)

32
Q

for synthase the deP form is the active/inactive form

A

for synthase the deP is the Active form

33
Q

for phosphorylase kinase & phosphorylase the deP form is the active/inactive form

A

for phosphorylase kinase & phosphorylase the deP is the Inactive form

34
Q

insulin’s role in glycogen metabolism

A
  1. inhibits several kinases = prevents P’lation of Synthase
    activates Phosphoprotein Phosphatase = Activates Synthase
  2. promotes conversion of cAMP -> 5’ AMP
    Net: activation of Glycogen Synthase (to its deP form)
    and thus Glycogen synthesis (storage)
35
Q

what are the allosteric effectors involved in glycogen metabolism?

A

Ca 2+
AMP
glucose
G-6-P

36
Q

Ca2+ allosterically acts on…

A

phosphorylase kinase b (deP inactive form)
Activating it

Note: Ca also phosphorylates and inhibits Glycogen Synthase
thus, Ca+ increases degradation and decreases synthesis of glycogen

Ca is also required for maximum activation of phosphorylase kinase a

37
Q

AMP allosterically acts on…

A

glycogen phosphorylase b (mm isozyme)
(inactive deP form)

AMP indicates low energy! so Activates the phosphorylase to breakdown glycogen stores

38
Q

Glucose allosterically acts on

A
phosphorylase a (liver isozyme)
(a- active, P form)

Glucose = energy available, so Glucose will Deactivate it bc we don’t need to make more energy

39
Q

Glucose 6 -P allosterically acts on

A

Glycogen Synthase b
(inactive, P form)

G-6-P indicates energy is available => Activates it to store available energy

40
Q

Differences in Ca2+ in muscle and liver

A

Contracting muscle:
Ach -> depolarization -> release of Ca2+ from sarcoplasmic reticulum

Liver:
Epi -> alpha-adrenergic receptors -> Phospholipase C -> IP3 (and DAG) -> release of Ca2+ from ER

41
Q

Epinephrine binding to beta-adrenergic receptors

A

in liver and muscle

promotes glycogenolysis via activation of cAMP -> PKA

42
Q

Epinephrine binding to alpha-adrenergic receptors

A
liver only
promotes glycogenolysis (increase blood sugar)
43
Q

Triacylglyceral/fat (TAG) synthesis and degradation site

A

synthesis; liver

degradation; fat

44
Q

dihydroxyacetone phosphate (DHAP)

A

can be converted to GAP (glyceraldehyde 3-phosphate) and sent into glycolysis

or continue on into TAG synthesis

45
Q

key lipase for TAG degradation

A

Hormone Sensitive Lipase

activated by Epinephrine (some degree glucagon)