structure and function of mitochondria and peroxisomes lecture eph 2015 láng, orsolya md, phd...
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Structure and function of mitochondria and peroxisomes
www.dgci.sote.huLecture EPh 2015
Láng, Orsolya MD, PhDDept. Genetics, Cell & Immunobiology, Semmelweis University
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Endosymbiotic theory – Similar Origin
Similarities: origin biogenesis metabolic activity: beta-oxidation
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Mitochondrion
By TEM By SEM
By Confocal M
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1894 - Richard Altmann established them as cell organelles and called them "bioblasts"1898 - The term "mitochondria" was coined by Carl Benda1900 - Leonor Michaelis discovered Janus Green can be used as a supravital stain
for mitochondria 1913 particles from extracts of guinea-pig liver were linked to respiration by Otto
Heinrich Warburg, which he called "grana".1948 - Albert Lester Lehninger described the oxidative phosphorylation
1952 - The first „official portrait” was taken by high resolution micrographs
1957 - The popular term "powerhouse of the cell" was coined by Philip Siekevitz
History
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Mitochondrion
Size
Width 0.2-3.0 mlength 7-10 m,
but dynamically changeable
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Inner membrane of Mch
crista
tubular
berry-likefingerprint-like
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Localisation
Striated duct cells
Sperm cell
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Number of mitochondria
Number/cellRBC, anaerobe cells of parasites – 0
ConstantSperm cell – 24
Dynamically changeableLeukocytes ~300Hepatocytes ~2000Increased number in hyperthyroid patients
Chaos-Chaos ameba - 500.000 !
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Fission and fusion
Drp1 (outer and inner membrane fission).
Fis1 ( works as receptor of Drp1)
Mitofusin protein (outer membrane fusion),
OPA1 (inner membrane fusion),
Drp1-dynamin-related protein 1, Drp1 Fis1 - Mitochondrial fission 1 proteinOpa1 - Optic Atrophy 1
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Dynamic mitochondria
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Composition I.compartmentalisation
Outer membrane• poor in proteins• characteristic protein: porin (b-sheet– trimers form channels)• permeability up to 5000 dalton•fatty acids, triptophane and adrenaline metabolizing enzymes are also localized in the outer membrane
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Outer membrane proteins in Mitochondria
apoptosisfission
channeltranslocators
and their function
What do you know about Tom40 ?
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Big flow of molecules across the membrane
Porin protein: transmembrane protein;
known from outer membranes of bacteria, mitochondria, and chloroplasts
Characterised by number of antiparallel β-strands and by the shear number
3 porins forms a chanel; <5000 Da can go through
bigger molecules are transported with active transport across the mitochondrial transporters
OM- Porin
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Composition II.
Inner membrane Increased surface 70% proteins: e- - transporter chaini ATP synthesis transporters
other point impermeable – 20% cardiolipin
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Proteins involved in oxidative phosphorylation
http://www.bio.davidson.edu/genomics/2004/Wilson/yeast%20protein.htm
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https://www.youtube.com/watch?v=GM9buhWJjlA
ATP synthase – molecular motor
Transmembrane proton carriers subunit
F1 ATP-asechatalytic site
Stator: a,b,dEnchore the structure
Rotor: ƐSpin clockwise when H+ enter
Matrix/IC
IMS / EC
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Terms of Chemiosmotic theory
• Mch. Respiratory chain – moves electrons - pumps H+ into
intermembrane space• Mch. ATP synthase works also as a H+ pump.
• Reversible mechanism:
• Several carrier molecules for metabolites, ions – in the inner membrane of Mch.
• Other point of the inner membrane of Mch. is impermeable for H+ and OH-.
H+ in ATP synthesis
ATP cleavageH+ out
Peter Dennis Mitchell
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Matrix
• Pyruvate dehydrogenase complex• Enzymes of citric acid cycle• Enzymes of ß-oxydation of fatty acids• Enzymes of amino acid oxydation
• 5-10 copies of mtDNA (circular)• Enzymes of mtDNA replication and transcription•Ribosomes (70S)
• ATP, ADP, Pi
• Mg2+, Ca2+, K+
Composition III.
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ATP synthesis Regulation of Ca2+ levels in the cell (cation granula) Lipid homeostasis (lipid oxidation, steroid synthesis) Nucleotide metabolism Amino acid metabolism FE-S synthesis (Hem) Ubiquinone synthesis Cofactor synthesis Apoptosis Aging Heat production
Function of Mitochondria
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Cellular respiration
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Upon one mol glucose oxidation, 36 mol ATPs are formed
in eukaryotes
mitochondrium
cytosolATP synthesis
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Szent-Györgyi – Kreb’s cycle
Formation of Acetyl-CoA
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Oxidative phosphorylation
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Oxygen absent – NAD regeneration by fermentation
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Heat production- thermogenesis It is activated whenever the organism is in need of extra heat: febrile state - centrally controlled via hypothalamusfeeding - low in protein diet, leptin-dependent hypothalamic control
Thermogenin = uncoupling protein 1
(UCP1)
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The human mitochondrial genome
MT-DNA is circular, double-stranded structures consists of 16’569 base pairs carrying the information for 37 genes.
http://www.mun.ca/biology/desmid/brian/BIOL2060/BIOL2060-18/18_25.jpg
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mt-DNA
• ring shape, 5 –10 copies/Mch.• 13 Mt genes are coding proteins• there are no introns• few regulator genes• no histons• replication, transcription, translation • 22 tRNA, 2 rRNA
Difference in protein synthesis: 70S ribobome protein synthesis starts w/ fMet antibiotic sensitivity
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• growth and proliferation of mitochondria are controlled by both nuclear genome and it’s own genome.
Semiautonomous organelle
Apx. 1000 proteins are distributed between the outer membrane, intermembrane space, inner membrane and matrix space
98 %
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Selective transport of proteins to Organells
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Major membrane components
TIM 23 complex
TIM 22 complex
OXA complex
SAMcomplex
TOMcomplex
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Direct import of unfolded protein into matrix
1
2
3
4
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Further requirements
Chaperons – both cytosolic and mitochondrial HSP70
IM Membrane potential
Energy- ATP hydrolysis
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Integration of unfolded protein into OM
Beta - signal in C terminus Chaperons bids to the protein in IMS SAM complexes insert the protein inOM
What kind of protein can be inserted in OM?
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Integration of protein into IM I.
N-terminus signal sequence Hydrophobic sequence TIM23 stops translocation
N-terminus signal sequence Hydrophobic sequence – 2nd signal OXA complex folds it Mitochondrial proteins as wellName one protein!
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Integration of protein into IM II.
Metabolite transporters have internal signal sequence – loop in TOM Chaperons in IMS TIM22 is specialized for insertion of multipass IM proteins
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Which pathway can be used for IMS proteins ?
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http://www.biochemie.uni-freiburg.de/ag/pfanner/research
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https://www.qiagen.com/geneglobe/static/images/pathways/mitochondrial%20protein%20import%20pathways.jpg
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Mathernal inheritance
2015. February
U.K. Parliament approves controversial three-parent mitochondrial gene therapy
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Mutation rate of mtDNA based familyTree
https://abagond.wordpress.com/2010/01/08/mitochondrial-dna/
-week repair mechanism
- high mutation rate 100 times faster than in the nucleus
in 1980s Allan Wilson tested the mtDNA of 137 people from different parts of the world.
Everyone alive today came from a single woman who lived in Africa about 200,000 years ago: Mitochondrial Eve.
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Mitochondrial disorders and dysfunctions
Primary events
Secondray!
!
!
!
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Mitochondrial disorders can be caused by mutations: in mitochondrial DNA (mtDNA) or in nuclear genes that code for mitochondrial components.
Most sensitive cells are:NeuronsMuscell cells
Can be acquired mitochondrial dysfunction due to adverse effects of drugs, infections, or other environmental causes
http://www.icmr.nic.in/ijmr/2015/janaury/0103.pdf
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http://www.icmr.nic.in/ijmr/2015/janaury/0103.pdf
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Mt-DNA
• Leber's Hereditary Optic Neuropathy (Complex I)
Nuclear DNA – mt-proteins
• Congenital muscular dystrophy
Mitochondria with paracrystalline
Both eyes are affected
Reason: nervus opticus (optical nerve) and retina cells dye because
Mechanism : cause defects in several NADH-ubiquinone oxidoreductase chains, therefore impair glutamate transport and increase reactive oxygen species level
Inherited mitochondrial disorders
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Pharmacological aspects of Mtch
http://www.cell.com/trends/pharmacological-sciences/fulltext/S0165-6147%2812%2900042-9
Strategies for mitochondrial pharmacology: to make molecules selectively accumulate within mitochondria. to use molecules that bind targets within mitochondria to modulate processes outside mitochondria that ultimately alter mitochondrial function
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1. Circular mt DNA (Non-Mendelian inheritence) Animal mt: smallest genetic system known Translation of 13 polypeptide 2. Size of mitoribosomes (70 S) 3. Formylmethionine initiator amino acid 4. Antibiotic sensitivity 5.Presence of porin in Gram negative bacteria 6. Similarities of the electron transport chain and ATP synthase 7. Division of mitochondria
Proofs of bacterial origin
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Peroxisome
By TEM By SEM
By Confocal M
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Structure
0,3-1,5 µm single membrane bound organelle Oxidative enzymes :
Catalase Ureate oxidase crystalloid – not in human
Selective import No genome - No Transcription, No translation
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Peroxisomal membrane proteins (PMP):
- peroxins (genes: PEX)
- other PMP e.g. „half „ ABC transporters)
Composition I.
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Peroxisomal matrix:
Enzymes of oxidative processes: Superoxid dismutase, catalase, peroxidase,
Enzymes of metabolic pathways: fatty acid oxidation, bile acid synthesis, enzymes of purin metabolism
Composition II.
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Glyoxysome• Specialized peroxisome for
Glyoxylate cycle – photorespiration in plant cels
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Function of peroxisome
Neutralisation of O2 radicals
Oxidative processes:Synthesis and degradation of hydrogen peroxideOxidation of long-chain fatty acids (fatty acids with 24 to 26 carbons) Fatty acid oxidation ( oxidation) Purin metabolism D amino acid oxidationRetinoid metabolism
Detoxification:Catalases uses some parts of it to detoxify alcohols in liver cells
Synthesis: Synthesis of cholesterol and bile acids in the liverSynthesis of certain phospholipids(plasmalogen) in neurons
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Summary of lipid metabolism in Peroxisome
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Biogenesis of Peroxisome
1.
2.
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Sheme of matrix protein import
http://www.nature.com/nrm/journal/v3/n5/fig_tab/nrm807_F1.html
1. binding of enzymes (red circles) by the import receptors (PEX5);
2 transport of receptor–enzyme complexes to the peroxisome surface;
3 docking of with peroxisomal membrane proteins, (PEX14 ,PEX13);
4 dissociation 5 receptor recycling,
Requirements : PTS signal: Ser-Lys-Leu(SKL) at C terminus of the protein most of the 24 pex gene products
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PEX molecules
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PTS1R = Pex5
Catalase is transported in tetramer formnot in an unfolded form
Import of matrix protein: catalase enzyme
PTS1 signal
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PBDs
(peroxisome biogenesis disorders)
PSEDs
(peroxisomal single enzyme disorders)
Main forms of peroxisomal disorders
PEX gene mutations
Defective –Import Empty peroxisomesHypomyelination
Symptomes:HypotoniaHepatomegaly
enzymopathy
X linked Adrenoleukodystrophy
Most serius for is Zellweger syndrome
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X-linked Adrenoleukodystrophy Mutation of ABCD1 transporter
accumulation of very long chain fatty acids in tissues throughout the body,
many different phenotypes
most severely affected tissues are the myelin in the central nervous system, the adrenal cortex and the Leydig cells
Teratment: Diet - restricting the intake of very-long chain fatty
acids (VLCFA) Lorenzo's oil : mixture of unsaturated fatty acids
(glycerol trioleate and glyceryl trierucate in a 4:1 ratio), known as inhibits elongation of saturated fatty acids in the body.
Future - Gene therapy
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Chloroplast
By TEM By SEM
By LM
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Chloroplast
Highly structured, membrane rich organelle:1. double-membrane envelope2. stroma: large soluble interior3. thylakoid membrane system - granum4. intrathylakoid space or lumen
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1. many important biochemical (anabolic) pathways, e.g., photosynthesis
starch synthesis fatty acid synthesisamino acids synthesispigment synthesisnucleotide synthesisnucleic acids and protein synthesissulfur and nitrogen assimilation
2. own genetic machinery* * Indicates that pathway involves a chloroplast encoded
gene in at least some organisms
Functions
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http://www.nature.com/nrm/journal/v12/n1/fig_tab/nrm3027_F1.html
Protein transport I.
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Protein transport II.
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From Kolodner & Tewari
“relaxed” cpDNA molecule from lettuce
Chloroplast DNA (cpDNA)
General features:1. double-stranded,
circular molecule2. no histones, but have
bound proteins (e.g., Hu), organized into nucleoids
3. G-C content typically less than nuclear DNA
4. multiple copies (~30-100) per plastid (i.e., all cp genes are multi-copy)
5. can be 10-20% of the total DNA in leaves
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Reproduction
• all plant and eukaryotic algal cells have plastids
• chloroplasts form by division; semi-autonomous
• Involves proteins (Fts) similar to those that mediate
cell division in bacteria
From Miyagishima et al.
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Photorespirationoccurs when the CO2 levels inside a leaf become low
Rubisco starts to combine O2 with RuBP instead of CO2.