heme synthesis prof.dr.arzu seven. heme synthesis heme is synthesized from porphyrins and iron....
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HEME SYNTHESIS
Prof.Dr.Arzu SEVEN
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HEME SYNTHESIS
• Heme is synthesized from porphyrins and iron.
• Porphyrins are cyclic compounds formed by the linkage of four pyrole rings through –HC =methenyl bridges
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• A characteristic property of porphyrins is to form complex with metal ions :
_iron porhyrins heme _mg containing porphyrins
chlorophyll
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• Metalloporphyrins and hemoproteins are important in nature .
• Natural porphyrins have substutient side chains for the 8 hydrogen atoms on the porphrin nucleus (C20H14N4)
• The substituents : A:acetate P:propionate V:vinly(_CH_CH2) M:methyl
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• A porhyrin with a completely symmetric arrangement of substituents is classified as type I porphyrin
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• A porphyrin with asymetric substitution in ring IV is classified as type III porhyrin
• Only types I and III are found in nature, type III series are for more abundant
• Heme and its immediate precursor -protoporphyrin IX -are type III porphyrins
(asymetric distribution of methyl groups in ring IV)
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• Hem is synthesized from succinyl-CoA and glycine.
• Pyroxal phosphate is necessary to activate glycine.
• Enzyme: ALA synthase (rate controlling enzyme in
porphyrin synthesis in mammalian liver)
• location:mitochondria
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• In the cytosol .2 mol of ALA condense by ALA dehydratase to form 2 mol of H2O and porphobilinojen (PBG)
• ALA dehydratase is a zinc containing enzyme, sensitive to inhibition by lead (lead poisoning)
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• 4 mol of PBG condense to form a linear tetrapyrole, hydroxymethybilane(HMB)
enzyme:uroporphrinogen I synthase(PBG deaminase , HMB synthase)
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• HMB cyclizes spontaneously to form uroporphyrinogen I or is converted to uroporphyrinogen III by uroporphyrinogen III synthase
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-the pyrole rings in uroporphyrinogen I and III are connected by methylene bridges(-CH2-) and do not form conjugated ring systems .
-All the porphyrinogens are colorless. -They are readily auto_oxidized to their
respective colored porphyrins, catalyzed by light and by the porphyrins formed.
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• Uroporphrinogen III and I are converted to porphyrinogen III and I by decarboxylation (AM)
enzyme:uroporphrinogen decarboxylase
• Coproporphyrinogen III enters the mitochondria protoporphyrinogen III protoporphyrin III
oxidase
oxidase
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• Formation of heme involves incorporation of ferrous iron into protoporphyrin
enzyme:ferrochelatase(heme synthase)
location:mitochondria
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• Heme synthesis occurs in most mammalian cells except mature erythrocytes (no mitochondria)
• 85% of heme synthesis occurs in erythroid precursor cells in bone marrow, the rest in hepatocytes.
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Regulation of heme synthesis:
• ALA synthase (ALAS1) is the key regulatory enzyme in hepatic biosynthesis of heme
-ALAS1HEPATİC -ALAS2ERYTHROİD
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• Heme, through an aporepressor molecule, acts as a negative regulator of ALAS1
• Heme affects translation of ALAS1 and its transfer from cytosol to mitochondrion.
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• Drugs(barbiturates,griseofulvin) that are metabolized in the liver by using cytocrome p450,decrease intracellular heme concentration derepress(induce) ALAS1 heme synthesis increases.
• Glucose loading and hematin administration can repress ALAS1 in liver.
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PORHYRINS
• The characteristic absorption spectrum of porphryrins _the sharp absorbtion band near 400 nm_ is of great value SORET BAND
• When porphyrins,dissolved in strong mineral acids or in organic solvents , are illuminated by UV light,they emit a strong red fluorescence.
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• The double bonds joining the pyrole rings in the porphyrins are responsible for the characteristic absorption and fluorescence of porphyrins.
-At 400 nm the porphyrins react with molecular oxygen to form oxygen radicals.
Lysosomes and other organelles are injured Degradative enzymes are released skin damage (scarring)
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• Due to the photodynamic properties of porphyrins,they are used in cancer phototherapy.
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PORPHYRİA
• Disorders due to abnormalities in the heme biosynthesis pathway
• Genetic or acquired
• Autosomol dominant manner
• Congenital erythropoietic porphyria (recessive)
• Diagnosis Clinical γ family history
Physical examination
Assay of the activity of the responsible enzyme (red blood cells)
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• Prenatal diagnosis (gene probes)• Porphyrias can be classified according to organs
or cells that are most affected :Erythropoietic or hepatic
• Drugs that induce cytocrome P 450 can precipitate porphyria attacks.
• High levels of LEAD combine with –SH groups of ferrochelatase and ALA dehydratase protoporphyrin (erythrocytes)
• ALA ,coproporphyrin (urine)
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• Treatment:– Symptomatic– Avoid drugs that induce cyt P450– Glucose _loading– Hematin administration– β carotenePhotosensitivity decreases