Scale in - Hellas · 2010-11-05 · 30 Import into the matrix - 2Import into the matrix - 2 This is...
Transcript of Scale in - Hellas · 2010-11-05 · 30 Import into the matrix - 2Import into the matrix - 2 This is...
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Scale in the biological world
Scale in the biological world
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A cellseen by TEM
A cellseen by TEM
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From living cells to atoms
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Compartmentalisation in the cell:internal membranes and the cytosol
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The Origin of mitochondria:The endosymbion hypothesis
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The cytosol:more than just H2O
Ribosomes
Proteins
RNAs
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Living cells obey the laws of thermodynamics
Living cells are NOT isolated systems:
Cells take energy from the environment (chemicals ie foodstuffsor photons ie sunlight) to generate order ie assemblies
In doing so, they dischagre HEAT to the environment
This increases the total ENTROPY
Energy conversion is vital for the cell
Mitochondria biogenesis and function
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The Eukaryotic Cell
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Different ways to target proteins in the cellDifferent ways to target proteins in the cell
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Mitochondria are essential for life
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Energy Conversion: Mitochondria and Chloroplasts Energy Conversion: Mitochondria and Chloroplasts
MembraneMembrane--boundedbounded
Occupy a major fraction of cell volumeOccupy a major fraction of cell volume
Large amount of Large amount of internalinternal membranemembrane
Common pathway for energy Common pathway for energy conversion: conversion: ChemiosmoticChemiosmotic couplingcoupling
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Chemiosmotic couplingChemiosmotic coupling
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1. Substantial portion of cell volume1. Substantial portion of cell volumeAbout 20% of the volume of a eukaryotic cellAbout 20% of the volume of a eukaryotic cellMitochondrial IM is 1/3 of total cell membraneMitochondrial IM is 1/3 of total cell membrane
2. Mitochondrial function supplies 30 2. Mitochondrial function supplies 30 ATP molecules (only 2 ATP from anaerobic ATP molecules (only 2 ATP from anaerobic ((cytosoliccytosolic) ) glycolysisglycolysis
3. Mobile, shape3. Mobile, shape--changing,fusion/separationchanging,fusion/separation
The MitochondrionThe Mitochondrion
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EM view of a Mitochondrion
3D Reconstruction
mobile, shape-changing
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Large GTPases control mitochondrial
fusion (Fzo1, OM)
fission (Dnm1, OM)
and
Inner membrane remodelling(Mgm1, IMS)
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Outer Membrane (Outer Membrane (semipermeablesemipermeable))6% of total 6% of total mit.proteinmit.proteinlipid metabolism enzymes, lipid metabolism enzymes, porinporin
IMSIMS6% of total 6% of total mit.proteinmit.proteinenzymes that use ATP to enzymes that use ATP to phosphorylatephosphorylate other nucleotidesother nucleotides
Inner Membrane (impermeable)Inner Membrane (impermeable)21% of total 21% of total mit.proteinmit.proteinATP ATP synthasesynthase, respiratory chain enzymes, transport proteins, respiratory chain enzymes, transport proteins
MatrixMatrix67%67% of total of total mit.proteinmit.proteinHundreds of enzymes, DNA, Hundreds of enzymes, DNA, ribosomesribosomes, , tRNAstRNAs
Mitochondrial StructureMitochondrial Structure
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Mitochondrial Energy MetabolismMitochondrial Energy Metabolism
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The Electrochemical Proton GradientThe Electrochemical Proton Gradient
140 mV
60 mV(-1 pH unit)
TOTAL200 mV
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Active transport processes are driven by the electrochemical proton gradient
Active transport processes are driven by the electrochemical proton gradient
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The Respiratory chain consists of 3 large membrane-embedded enzyme complexes The Respiratory chain consists of 3 large membrane-embedded enzyme complexes
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ATP Synthase is a reversible coupling device: It interconverts the energies of the
electrochemical proton gradient and chemical bonds
ATP Synthase is a reversible coupling device: It interconverts the energies of the
electrochemical proton gradient and chemical bonds
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Functional Complexity
Respiration and ATP Synthesis
Synthesis of heme, lipids, amino acids and nucleotides
Intracellular homeostasisof inorganic ions
Structural Complexity
5-15% of total cell protein20% volume of eukaryotic cellIM is 1/3 of total cell membrane
About 1000 different polypeptides(600 in yeast)
Only a dozen encoded by mtDNA
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Protein import is the major mechanism
of mitochondriabiogenesis
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Identification of components of the Mitochondrial Protein Import System
Identification of components of the Mitochondrial Protein Import System
Genetic analyses (fungal genetics)Genetic analyses (fungal genetics)
In vitro import assay system with isolated In vitro import assay system with isolated functional mitochondriafunctional mitochondria
Chemical Chemical CrosslinkingCrosslinking
Biochemical reconstitutionBiochemical reconstitution
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IMPORT INTO YEAST MITOCHONDRIA
Proteins with N-terminal cleavable presequences:
Matrix proteins
Proteins with internal targeting signals:
AAC
OM
IMS
Matrix
IM
TIM10
TIM23
Hsp70Mge1
TIM22∆Ψ+
TOM
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Import into the matrix - 1Import into the matrix - 1
• Depends on a matrix-targeting signal: The presequence• Cleavable, usually located at the N-terminus•usually 12-15 residues long•amphiphilic, with positively charged residues on one side of an a-helix
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Presequence binding to Tom20
Endo and Kohda
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Import into the matrix - 2Import into the matrix - 2This is a This is a multistepmultistep processprocess
Interactions with chaperones in the Interactions with chaperones in the cytosolcytosol keep the keep the precursor in an unfolded conformation (“importprecursor in an unfolded conformation (“import--competent”)competent”)
Different import complexes in the OM (TOM complex) and Different import complexes in the OM (TOM complex) and the IM (TIM complex).the IM (TIM complex).
Electrostatic interactions between the positive Electrostatic interactions between the positive presequencepresequenceand negative patches of receptors along the import and negative patches of receptors along the import pathway: The Acid chain hypothesispathway: The Acid chain hypothesis-- Gradation of affinities Gradation of affinities leads the leads the presequencepresequence along the import pathwayalong the import pathway
The The electrophoreticelectrophoretic function of the potential across the IM function of the potential across the IM draws the precursor across the IMdraws the precursor across the IM
The pulling force of the translocation motor mHsp70/Tim44 The pulling force of the translocation motor mHsp70/Tim44 actively draws the precursor to complete translocationactively draws the precursor to complete translocation
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Import into the matrix - 3Import into the matrix - 3
Energy requirements:Energy requirements:
ATP HydrolysisATP HydrolysisIn the In the cytosolcytosol (function of (function of ATPaseATPase chaperones)chaperones)
In the mitochondrial matrix (Hsp70 translocation motor)In the mitochondrial matrix (Hsp70 translocation motor)
Electrochemical potential across the inner Electrochemical potential across the inner membranemembrane
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Import into the matrix - 4Import into the matrix - 4
ComponentsComponentsTOM Complex:TOM Complex:
Receptors: Tom70, Tom20, Tom37, Tom22Receptors: Tom70, Tom20, Tom37, Tom22
ChannelChannel--forming: Tom40, Tom5forming: Tom40, Tom5
Channel modulating: Tom6, Tom7Channel modulating: Tom6, Tom7
TIM Complex:TIM Complex:Receptor: Tim23Receptor: Tim23
ChannelChannel--forming: Tim23, Tim17forming: Tim23, Tim17
Translocation motor: Tim44, Hsp70, Translocation motor: Tim44, Hsp70, GrpEGrpE (co(co--chaperone)chaperone)
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Summary of Protein Import into the Mitochondrial Matrix
Summary of Protein Import into the Mitochondrial Matrix
I
II
III
IV
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Import into the IMS Import into the IMS
A. Variation of the matrix targeting A. Variation of the matrix targeting pathway pathway
example: example: cytochromecytochrome b2b2
B. Distinct pathway involving a specific IMS targeting B. Distinct pathway involving a specific IMS targeting signalsignal
example: mitochondrial example: mitochondrial hemeheme lyaseslyases
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Cytb2 IMS targeting - 1Cytb2 IMS targeting - 1
Bipartite nature: matrix targeting signal followed by an IMS Bipartite nature: matrix targeting signal followed by an IMS sorting signalsorting signal
IMS sorting signal contains mainly uncharged residuesIMS sorting signal contains mainly uncharged residues
cleaved by specific IMS proteasecleaved by specific IMS protease
NOT very highly conservedNOT very highly conserved
The Signal:
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Electrochemical potential absolutely essential but ATP hydrolysiElectrochemical potential absolutely essential but ATP hydrolysis NOT s NOT requiredrequired
Energetics:
Components:
Known Subunits of the TOM complexKnown Subunits of the TOM complex
TIM23 complexTIM23 complex
IMS sorting peptidaseIMS sorting peptidase
Cytb2 IMS targeting - 2Cytb2 IMS targeting - 2
Mechanism:Stop-transfer mechanism: the hydrophobic sorting signal is stuck at the TIM23 complex and laterally diffuses out into the lipid bilayer of the IM
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Import into the IMS Import into the IMS
A. Variation of the matrix targeting pathwayA. Variation of the matrix targeting pathwayexample: example: cytochromecytochrome b2b2
B. Distinct pathway involving a B. Distinct pathway involving a specific IMS targeting signalspecific IMS targeting signal
example: mitochondrial example: mitochondrial hemehemelyaseslyases
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Heme Lyase IMS targeting - 1Heme Lyase IMS targeting - 1
InternalInternal
about 60 residues longabout 60 residues long
highly conserved sequencehighly conserved sequence
highly hydrophilic (30% charged residues, similar number of + anhighly hydrophilic (30% charged residues, similar number of + and d --charged residues, distributed throughout the sequence)charged residues, distributed throughout the sequence)
mainly amainly a--helical, but NOT helical, but NOT amphiphilicamphiphilic
Key reference: Key reference: DiekertDiekert et al Proc. National Acad. et al Proc. National Acad. SciSci. USA 1999, 96, 11752. USA 1999, 96, 11752--1175711757
The Signal:
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The Mitochondrial Carrier Family• Function as metabolite transporters
• 37 proteins in yeast (10-15% of the total mitochondrial protein)
• 30-35 kDa
•Common topology: 3 similar repeated motifs(3X2 helix model)