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Protein Kinase A

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The title of this article should be cAMP-dependent protein kinase. The initial letter is capitalized due to technical restrictions.


In cell biology, protein kinase A (PKA, also known as cAMP-dependent protein kinase (cAPK) EC 2.7.11.11), refers to a family of enzymes whose activity is dependent on the level of cyclic AMP (cAMP) in the cell. Protein kinase A has several functions in the cell, including regulation of glycogen, sugar, and lipid metabolism.

MechanismEdit

ActivationEdit

Each PKA is a holoenzyme that consists of two regulatory and two catalytic subunits. Under low levels of cAMP, the holoenzyme remains intact and is catalytically inactive. When the concentration of cAMP rises (e.g. activation of adenylate cyclases by G protein-coupled receptors coupled to Gs, inhibition of phosphodiesterases which degrade cAMP), cAMP binds to the two binding sites on the regulatory subunits, which then undergo a conformational change that releases the catalytic subunits.

CatalyzationEdit

The free catalytic subunits can then catalyse the transfer of ATP terminal phosphates to protein substrates at serine, or threonine residues. This phosphorylation usually results in a change in activity of the substrate. Since PKAs are present in a variety of cells and act on different substrates, PKA and cAMP regulation are involved in many different pathways.

The mechanisms of further effects may be divided into direct protein phosphorylation and protein synthesis:

  • In direct protein phosphorylation PKA directly either increases or decreases the activity of a protein.
  • In protein synthesis PKA first directly activates CREB, which binds the cAMP response element, altering the transcription and therefore the synthesis of the protein. This mechanism generally takes longer time (hours to days).

Inactivation Edit

PKA is thus controlled by cAMP. Also, the catalytic subunit itself can be regulated by phosphorylation.

Downregulation of protein kinase A occurs by a feedback mechanism: one of the substrates that is activated by the kinase is a phosphodiesterase, which converts quickly cAMP to AMP, thus reducing the amount of cAMP that can activate protein kinase A.

FunctionEdit

PKA phosphorylates other proteins, altering their function. However, what proteins are available for phosphorylation depends on in what kind of cell the PKA activity is present, since protein composition varies from cell type to cell type. Thus, the effects of PKA varies with cell type:

Overview tableEdit

Cell type Organ/system Stimulators
ligands --> Gs-GPCRs
or PDE inhibitors
Inhibitors
ligands --> Gi-GPCRs
or PDE stimulators
Effects
adipocyte
myocyte (skeletal muscle) muscular system
hepatocyte liver
neurons in nucleus accumbens nervous system dopamine --> dopamine receptor Activate reward system
principal cells in kidney kidney
myocyte (smooth muscle) muscular system Vasodilation
Thick ascending limb cell kidney Vasopressin --> V2 receptor stimulate Na-K-2Cl symporter (perhaps only minor effect) [2]
Cortical collecting tubule cell kidney Vasopressin --> V2 receptor stimulate Epithelial sodium channel (perhaps only minor effect) [2]
Inner medullary collecting duct cell kidney Vasopressin --> V2 receptor
proximal convoluted tubule cell kidney PTH --> PTH receptor 1 Inhibit NHE3 --> ↓H+ secretion[5]
juxtaglomerular cell kidney renin secretion

In adipocytes, myocytes and hepatocytes Edit

Epinephrine and glucagon affect the activity of protein kinase A by changing the levels of cAMP in a cell via the G-protein mechanism, using adenylate cyclase. Protein Kinase A acts to phosphorylate many enzymes important in metabolism. Protein kinase A phosphorylates Acetyl-CoA carboxylase and pyruvate dehydrogenase. Allosteric regulation of these enzymes in such a manner has an inhibitory effect. Insulin will increase the level of phosphorylation of these enzymes, which will divert acetyl-coA down the lipogenesis pathway. Glucagon has an antagonistic effect.

In nucleus accumbens neuronsEdit

PKA helps transfer/translate the dopamine signal into cells. It has been found (postmortem) to be elevated in the brains of smokers, in the nucleus accumbens, which mediates reward and motivation: a part of the brain acted on by "virtually all" recreational drugs; as well as "in the area of the midbrain that responds to dopamine, which acts as a 'reward chemical' in smokers and former smokers." [7]

See alsoEdit

ReferencesEdit

  1. 1.0 1.1 1.2 1.3 1.4 Rang, H. P. (2003). Pharmacology, Edinburgh: Churchill Livingstone. Page 172
  2. 2.0 2.1 2.2 2.3 2.4 Walter F., PhD. Boron. Medical Physiology: A Cellular And Molecular Approaoch, Elsevier/Saunders. Page 842
  3. Receptor-mediated activation of nitric oxide synthesis by arginine in endothelial cells Mahesh S. Joshi*,{dagger}, T. Bruce Ferguson, Jr.*, Fruzsina K. Johnson{ddagger}, Robert A. Johnson{ddagger}, Sampath Parthasarathy§, and Jack R. Lancaster, Jr.
  4. Walter F., PhD. Boron. Medical Physiology: A Cellular And Molecular Approaoch, Elsevier/Saunders. Page 844
  5. Walter F., PhD. Boron. Medical Physiology: A Cellular And Molecular Approaoch, Elsevier/Saunders. Page 852
  6. 6.0 6.1 6.2 6.3 Walter F., PhD. Boron (2003). Medical Physiology: A Cellular And Molecular Approaoch, 1300, Elsevier/Saunders. Page 867
  7. http://news.bbc.co.uk/2/hi/health/6378179.stm

External linksEdit



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