![Page 1: Oxidative phosphorylation Biochemistry, 4 th edition, RH Garrett & CM Grisham,](https://reader034.vdocuments.us/reader034/viewer/2022050821/5681658d550346895dd85806/html5/thumbnails/1.jpg)
Oxidative phosphorylationBiochemistry, 4th edition, RH Garrett & CM Grisham, Brooks/Cole (Cengage); Boston, MA: 2010
pp 592-629
Instructor: Kirill Popov
![Page 2: Oxidative phosphorylation Biochemistry, 4 th edition, RH Garrett & CM Grisham,](https://reader034.vdocuments.us/reader034/viewer/2022050821/5681658d550346895dd85806/html5/thumbnails/2.jpg)
1. The mitochondrion
2. Electron transport
3. Oxidative phosphorylation
4. Heat, oxidative stress, etc.
![Page 3: Oxidative phosphorylation Biochemistry, 4 th edition, RH Garrett & CM Grisham,](https://reader034.vdocuments.us/reader034/viewer/2022050821/5681658d550346895dd85806/html5/thumbnails/3.jpg)
ATP synthase
Cristae
Ribosomes
Porin channels
Outer membrane
freely permeable tosmall molecules and ions
Inner membrane
Impermeable to mostsmall molecules and ionsIncluding H+
Contains:• Respiratory electron carriers• ADP/ATP translocase• ATP synthase• Other membrane transporters
Matrix
Contains:• Pyruvate dehydrogenase complex• Citric acid cycle enzymes• Fatty acid β-oxidation enzymes• Amino acid oxidation enzymes• DNA, ribosomes• Other enzymes and metabolites
Biochemical anatomy of a mitochondrion
![Page 4: Oxidative phosphorylation Biochemistry, 4 th edition, RH Garrett & CM Grisham,](https://reader034.vdocuments.us/reader034/viewer/2022050821/5681658d550346895dd85806/html5/thumbnails/4.jpg)
)10(
CH3
CH2 C CH2
CH3
CH2CH3O
CH3O
O
O
H
H+ + e−
Ubiquinone (Q)(fully oxidized)
H
CH3
CH3O
CH3O
O
OR
H
•
CH3
CH3O
CH3O
O
O
RH
H+ + e−
Semiquinone radical(•QH)
Ubiquinol (QH2)(fully reduced)
![Page 5: Oxidative phosphorylation Biochemistry, 4 th edition, RH Garrett & CM Grisham,](https://reader034.vdocuments.us/reader034/viewer/2022050821/5681658d550346895dd85806/html5/thumbnails/5.jpg)
Iron protoporphyrin IX(in b-type cytochromes)
Heme A(in a-type cytochromes)
Heme C(in c-type cytochromes)
N
N
NN
H3C CH
CH3
CH2CH2COO-
CH2CH2COO-H3C
H3C
CH
CH2
H2C
Fe
N
N
NN
H3C CHCH3
CH3
CH2CH2COO-
CH2CH2COO-H3C
H3C
CH3CH
S
S Cys
Cys
Fe
Fe
N
N
NN
H3C CH
CH3
CH2CH2COO-
CH2CH2COO-CHO
H3C
CH
CH2
CH2
OH
H3C
CH3CH3CH3
Prosthetic groups of cytochromes
![Page 6: Oxidative phosphorylation Biochemistry, 4 th edition, RH Garrett & CM Grisham,](https://reader034.vdocuments.us/reader034/viewer/2022050821/5681658d550346895dd85806/html5/thumbnails/6.jpg)
50
Rel
ativ
e lig
ht a
bsor
ptio
n (%
)
Wavelength (nm)
400 500 600300
100
0
γ
Oxidizedcyt c
Reducedcyt c
α
β
Adsorption spectra of cytochrome c
![Page 7: Oxidative phosphorylation Biochemistry, 4 th edition, RH Garrett & CM Grisham,](https://reader034.vdocuments.us/reader034/viewer/2022050821/5681658d550346895dd85806/html5/thumbnails/7.jpg)
Fe SCys
Fe
Fe
FeFeFe
Fe
SS
S
S
S S
S
S
S
S
S
S
S
S
S
S
SCys
CysCys
Cys Cys
Cys
Cys
Cys
Cys
Cys
Cys
Protein
Iron-sulfur centers
![Page 8: Oxidative phosphorylation Biochemistry, 4 th edition, RH Garrett & CM Grisham,](https://reader034.vdocuments.us/reader034/viewer/2022050821/5681658d550346895dd85806/html5/thumbnails/8.jpg)
Standard Reduction Potentials of Respiratory Chain and Related Electron Carriers
Redox reaction (half-reaction) E'° (V)
2H+ + 2e− → H2 -0.414
NAD+ + H+ + 2e− → NADH -0.320
NADP+ + H+ + 2e− → NADPH -0.324
NADH dehydrogenase (FMN) + 2H+ + 2e− → NADH dehydrogenase (FMNH2) -0.30
Ubiquinone + 2H+ + 2e− → ubiquinol 0.045
Cytochrome b (Fe3+) + e− → cytochrome b (Fe2+) 0.077
Cytochrome c1 (Fe3+) + 2e− → cytochrome c1 (Fe2+) 0.22
Cytochrome c (Fe3+) + 2e− → cytochrome c (Fe2+) 0.254
Cytochrome a (Fe3+) + 2e− → cytochrome a (Fe2+) 0.29
Cytochrome a3 (Fe3+) + 2e− → cytochrome a3 (Fe2+) 0.35
1/2O2 + 2H+ + 2e− → H2O 0.8166
![Page 9: Oxidative phosphorylation Biochemistry, 4 th edition, RH Garrett & CM Grisham,](https://reader034.vdocuments.us/reader034/viewer/2022050821/5681658d550346895dd85806/html5/thumbnails/9.jpg)
Separation of functional complexes of the respiratory chain
![Page 10: Oxidative phosphorylation Biochemistry, 4 th edition, RH Garrett & CM Grisham,](https://reader034.vdocuments.us/reader034/viewer/2022050821/5681658d550346895dd85806/html5/thumbnails/10.jpg)
The Protein Components of the Mitochondrial Electron-Transfer Chain
Enzyme complex/protein Mass (kDa) Number of subunits* Prosthetic group(s)
I NADH dehydrogenase 850 43 (14) FMN, Fe-S
II Succinate dehydrogenase 140 4 FAD, Fe-S
III Ubiquinone:cytochrome c oxidoreductase 250 11 Hemes, Fe-S
Cytochrome c# 13 1 Heme
IV Cytochrome oxidase 160 13 (3-4) Hemes, CuA, CuB
*Numbers of subunits in the bacterial equivalents in parentheses.#Cytochrome c is not part of an enzyme complex; it moves between Complexes III and IV as a freely soluble protein.
![Page 11: Oxidative phosphorylation Biochemistry, 4 th edition, RH Garrett & CM Grisham,](https://reader034.vdocuments.us/reader034/viewer/2022050821/5681658d550346895dd85806/html5/thumbnails/11.jpg)
Flavoprotein 4
Flavoprotein 1
Flavoprotein 2
Glycerolphosphatedehydrogenase,
FAD,Fe-S centers,
Flavoprotein 3
NADH dehydrogenase,FMN,
Fe-S centers
Succinate dehydrogenase,FAD,
Fe-S centers,b-type heme
Cytochrome bc1 complex,2 b-type hemes,
Rieske Fe-S centerc-type heme (cyt c1),
Electron-transferringf lavoprotein, FAD,
Fe-S centers,
Cytochrome cCytochrome aa3 complex,
2 a-type hemes,Cu ions
Complex IV
Complex II
Complex III
UQ/UQH2pool
Complex I
Fatty acyl-CoA dehydrogenase
NADH coenzyme Qoxidoreductase
Coenzyme Q-cytochrome coxidoreductase
Succinate-coenzyme Qoxidoreductase
Cytochrome c oxidase
H2O1/2 O2
Pathways in the mitochondrial electron transport
![Page 12: Oxidative phosphorylation Biochemistry, 4 th edition, RH Garrett & CM Grisham,](https://reader034.vdocuments.us/reader034/viewer/2022050821/5681658d550346895dd85806/html5/thumbnails/12.jpg)
Complex IV
NA
D+ /
NA
DH
FMN
(Fe/
S)N
2(F
e/S
)N3
(Fe/
S)N
4(Fe/
S)N
1
Complex I
Complex IIComplex III
Rie
ske
Fe/S
(Fe/
S)S
1
(Fe/
S)S
3FA
D
Fum
/Suc
c
UQ
10
b Lb H
c 1 c
Cu A
a 3
a
-200
+200
+400
+600
0
-400
E(m
V)
Electrons move downhill
![Page 13: Oxidative phosphorylation Biochemistry, 4 th edition, RH Garrett & CM Grisham,](https://reader034.vdocuments.us/reader034/viewer/2022050821/5681658d550346895dd85806/html5/thumbnails/13.jpg)
FMN
Fe-S
NAD+
NADH + H+
Intermembranespace (P side)
Matrix (N side)
Matrix arm
2e−
Seriesof Fe-Scenters
N-2Q
QH22e−
2H+
4H+
Membranearm
Complex I
NADH:ubiquinon oxidoreductase (Complex I)
![Page 14: Oxidative phosphorylation Biochemistry, 4 th edition, RH Garrett & CM Grisham,](https://reader034.vdocuments.us/reader034/viewer/2022050821/5681658d550346895dd85806/html5/thumbnails/14.jpg)
Q
Intermembranespace (P side)
Matrix (N side)2H+
QH2
Fe-S
FAD
2e−
Seriesof Fe-Scenters
2e−
b-type heme
Substratebinding
site
Ubiquinone
Succinate Fumarate
α-Ketoglutarate
Malate
Oxaloacetate
CitrateIsocitrate
Succinyl-CoA
Acetyl-CoA
Krebs cycle
Succinate dehydrogenase (Complex II)
![Page 15: Oxidative phosphorylation Biochemistry, 4 th edition, RH Garrett & CM Grisham,](https://reader034.vdocuments.us/reader034/viewer/2022050821/5681658d550346895dd85806/html5/thumbnails/15.jpg)
Cytochrome b
Heme
Cytochromec1
Cytochromec
2Fe-2Scenter
Rieske iron-sulfur protein
Intermembranespace (P side)
Matrix (N side)
c1
bL
bH
Qp
QN
Cytochrome bc1 complex (Complex III)
![Page 16: Oxidative phosphorylation Biochemistry, 4 th edition, RH Garrett & CM Grisham,](https://reader034.vdocuments.us/reader034/viewer/2022050821/5681658d550346895dd85806/html5/thumbnails/16.jpg)
Intermembranespace (P side)
Matrix (N side)
bL
bH
bL
bH
Cyt c1
Cyt cCyt c
Cyt c1
QH2
2H+
2H+2H+
Q
Q Q•Q•
QH2QH2
Oxidation of first QH2 Oxidation of second QH2
Q
Fe-S Fe-S
QH2 + Cyt c1 (oxidized) → Q•− + 2HP
+ + Cyt c1 (reduced)QH2 + Q•− + Cyt c1 (oxidized) →
QH2 + 2HP+ + Q + Cyt c1 (reduced)
Net equation:QH2 + 2 Cyt c1 (oxidized) + 2HN
+ → Q + 2 Cyt c1 (reduced) + 4HP+
The Q cycle
![Page 17: Oxidative phosphorylation Biochemistry, 4 th edition, RH Garrett & CM Grisham,](https://reader034.vdocuments.us/reader034/viewer/2022050821/5681658d550346895dd85806/html5/thumbnails/17.jpg)
4H+
(substrate)
Intermembranespace(P side)
2H2O2H+
(pumped)
4Cyt c4e-
O2
2H+
CuA
CuB
a
a3
I
IIIII
Fe-Cu center
Path of electrons through comlex IV
![Page 18: Oxidative phosphorylation Biochemistry, 4 th edition, RH Garrett & CM Grisham,](https://reader034.vdocuments.us/reader034/viewer/2022050821/5681658d550346895dd85806/html5/thumbnails/18.jpg)
CuFe
Cu
Cu
Cu
Cu
Cu
Fe
Fe
Fe
Fe
Fe
O2
O
O
O−
O
2+
O
O−
2H+
H HH+ H+2H2O
1+
1+
2+
2+
2+
2+
2+3+3+
3+
4+
1st e−
2nd e−
3rd e−4th e−
next cycle
Reaction sequence for the reduction of O2 by the cytochrome c oxidase
![Page 19: Oxidative phosphorylation Biochemistry, 4 th edition, RH Garrett & CM Grisham,](https://reader034.vdocuments.us/reader034/viewer/2022050821/5681658d550346895dd85806/html5/thumbnails/19.jpg)
The flow of electrons and protons through the respiratory chain (proton-motive force and chemiosmotic model)
IntermembraneSpace (P side)
Matrix (N side)II
I
IV
ADP +Pi ATP
Fo
F1
NADH + H+ NAD+ Succinate Fumarate
H2O1/2O2 + 2H+
4H+ 4H+
Q
Cyt c
III
2H+
Cyt c
H+
+ + + + + + + + + + + + + +
-------
Chemicalpotential
ΔpH(inside
alkaline)
ATPsynthesisdriven by
proton-motiveforce
Electricalpotential
Δψ(inside
negative)
ΔG = RT ln (C2/C1) + ZFΔψ= 2.3RT ΔpH + FΔψ
H+
H+
H+
H+
H+
H+
H+
H+
OH−
OH−
OH−
OH−
OH−
OH−
OH−
[H+]P = C2 [H+]N = C1
N sideP side
Protonpump
![Page 20: Oxidative phosphorylation Biochemistry, 4 th edition, RH Garrett & CM Grisham,](https://reader034.vdocuments.us/reader034/viewer/2022050821/5681658d550346895dd85806/html5/thumbnails/20.jpg)
H2O
P ATP
ATPP
H+H+
Enzyme bound
In the absence of a proton gradient:
In the presence of a proton gradient:
is releasedADP +
ADP + ADP +-
18O P OH
O-
O18OH2
Catalytic mechanism of F1
![Page 21: Oxidative phosphorylation Biochemistry, 4 th edition, RH Garrett & CM Grisham,](https://reader034.vdocuments.us/reader034/viewer/2022050821/5681658d550346895dd85806/html5/thumbnails/21.jpg)
Mitochondrial ATP synthase complex
![Page 22: Oxidative phosphorylation Biochemistry, 4 th edition, RH Garrett & CM Grisham,](https://reader034.vdocuments.us/reader034/viewer/2022050821/5681658d550346895dd85806/html5/thumbnails/22.jpg)
Rotation of Fo and γ
αβ ATP
ADP + Pi
α
C10a
b
γ
His residuesHis residues
Ni complex
Actin filament
Avidin
ε
![Page 23: Oxidative phosphorylation Biochemistry, 4 th edition, RH Garrett & CM Grisham,](https://reader034.vdocuments.us/reader034/viewer/2022050821/5681658d550346895dd85806/html5/thumbnails/23.jpg)
Rotation of Fo and γ
![Page 24: Oxidative phosphorylation Biochemistry, 4 th edition, RH Garrett & CM Grisham,](https://reader034.vdocuments.us/reader034/viewer/2022050821/5681658d550346895dd85806/html5/thumbnails/24.jpg)
N side
P side
C10a
b2
α β
γ
ε
ATP
ADP + Pi
δ β
H+
H+
F1
Fo
A model of the FoF1 complex, a rotating molecular motor
![Page 25: Oxidative phosphorylation Biochemistry, 4 th edition, RH Garrett & CM Grisham,](https://reader034.vdocuments.us/reader034/viewer/2022050821/5681658d550346895dd85806/html5/thumbnails/25.jpg)
ATP
ADP+ Pi
ATP
ATP
ATP
ATP
ATP
ADP+ Pi
ADP+ Pi
α
β
α
α
α
α
α
α
α
α
β
β
β
β
β
β
β
β
3 HP+
3 HN+
3 HN+
3 HN+
3 HP+
3 HP+
Binding-change model for ATP synthase
![Page 26: Oxidative phosphorylation Biochemistry, 4 th edition, RH Garrett & CM Grisham,](https://reader034.vdocuments.us/reader034/viewer/2022050821/5681658d550346895dd85806/html5/thumbnails/26.jpg)
The P/O ratio is an index of the efficiency of coupling
P/O ratio: number of molecules of Pi incorporated (=ATP synthesized) per atom of oxygen consumed (or pair of electrons being carried through the chain).
Measurements: oxygen consumption during complete phosphorylation of a fixed amount of ADP after addition of either an NAD+-linked substrate or FAD-linked substrate.
P/O 2.5 for NADHP/O 1.5 for FADH2
![Page 27: Oxidative phosphorylation Biochemistry, 4 th edition, RH Garrett & CM Grisham,](https://reader034.vdocuments.us/reader034/viewer/2022050821/5681658d550346895dd85806/html5/thumbnails/27.jpg)
Intermembranespace
Matrix
Adeninenucleotidetranslocase(antiporter)
H+ H+
H+
ADP3-
ATP4-
ATPsynthase
Phosphatetranslocase(symporter)
ADP3-
ATP4-
H+
H2PO4− H2PO4
−
Adenine nucleotide and phosphate translocases
![Page 28: Oxidative phosphorylation Biochemistry, 4 th edition, RH Garrett & CM Grisham,](https://reader034.vdocuments.us/reader034/viewer/2022050821/5681658d550346895dd85806/html5/thumbnails/28.jpg)
Matrix
Q III
Glycerol 3-phosphate
Dihydroxyacetonephosphate
NADH + H+NAD+
Glycolysis
cytosolicglyceol 3-phosphate
dehydrogenase
mitochondrialglyceol 3-phosphate
dehydrogenase
FADFADH2
CH2OH
C
CH2 O
O
P
CH2OH
CHOH
CH2 O P
Glycerol 3-phosphate shuttle
![Page 29: Oxidative phosphorylation Biochemistry, 4 th edition, RH Garrett & CM Grisham,](https://reader034.vdocuments.us/reader034/viewer/2022050821/5681658d550346895dd85806/html5/thumbnails/29.jpg)
Intermembranespace
Matrix
NADH + H+
α-Ketoglutarate
Malate Malate
OxaloacetateOxaloacetate
Aspartate Aspartate
Glutamate Glutamate
α-Ketoglutarate
Malateα-ketoglutaratetransporter
Glutamate-aspartatetransporter
malatedehydrogenase
aspartateaminotransferase
aspartateaminotransferase
malatedehydrogenase
NAD+ NAD+
H+ + NADH
Malate-aspartate shuttle
![Page 30: Oxidative phosphorylation Biochemistry, 4 th edition, RH Garrett & CM Grisham,](https://reader034.vdocuments.us/reader034/viewer/2022050821/5681658d550346895dd85806/html5/thumbnails/30.jpg)
ATP Yield from Complete Oxidation of GlucoseProcess Direct product Final ATP
Glycolysis 2 NADH (cytosolic)2 ATP
3 or 5*2
Pyruvate oxidation (two per glucose) 2 NADH (mitochondrial matrix) 5
Acetyl-CoA oxidation in citric acid cycle (two per glucose)
6 NADH (mitochondrial matrix)2 FADH2
2 GTP
1532
Total yield per glucose 30 or 32
*The number depends on which shuttle system transfers reducing equivalents into the mitochondrion.
![Page 31: Oxidative phosphorylation Biochemistry, 4 th edition, RH Garrett & CM Grisham,](https://reader034.vdocuments.us/reader034/viewer/2022050821/5681658d550346895dd85806/html5/thumbnails/31.jpg)
Intermembranespace
Matrix
Uncouplingprotein
(thermogenin)
Cyt c
H+
II
H+
H+
Heat
I
IV
III
ADP +Pi
ATP
Fo F1
Heat generation by uncoupled mitochondria
![Page 32: Oxidative phosphorylation Biochemistry, 4 th edition, RH Garrett & CM Grisham,](https://reader034.vdocuments.us/reader034/viewer/2022050821/5681658d550346895dd85806/html5/thumbnails/32.jpg)
Innermitochondrialmembrane
I
IVIII
Cyt c
Nicotinamidenucleotidetranshydrogenase
O2
•O2−
•OHNADH NAD+
NADPH
NAD+ NADP+ H2O2
superoxidedismutase
glutathioneperoxidase
H2O
GSSG
2 GSH
2 GSH
glutathionereductase
protein thiolreduction
GSSG
inactive
oxidativestress
active
EnzS
SSH
SH
Q
ROS formation in mitochondria and mitochondrial defenses
![Page 33: Oxidative phosphorylation Biochemistry, 4 th edition, RH Garrett & CM Grisham,](https://reader034.vdocuments.us/reader034/viewer/2022050821/5681658d550346895dd85806/html5/thumbnails/33.jpg)
HIF-1 increases transcriptionof other enzymes and proteins(green arrows)
Hypoxia (low pO2)
HIF-1
increasedlevelof HIF-1
Glucose
Glucosetransporter
Glycolyticenzymes
Pyruvate
ATP
ATP productionby glycolysisincreases
Acetyl-CoA
respiratory chainCitricacidcycle
ProteaseDegradesCOX4-1subunit
COX4-2subunit
ReplacesCOX4-1
NADH,FADH2
O2•O2
−, •OHElectron flow fromNADHand FADH2 toRespiratory chaindecreases
ROS production isreduced
Complex IV propertiesAre adapted to low pO2
lactatedehydrogenase
PDHkinase
pyruvatedehydrogenase(PDH)
O2
H2O
Complex IV
Lactate
Hypoxia-inducible factor (HIF-1)
![Page 34: Oxidative phosphorylation Biochemistry, 4 th edition, RH Garrett & CM Grisham,](https://reader034.vdocuments.us/reader034/viewer/2022050821/5681658d550346895dd85806/html5/thumbnails/34.jpg)
Procaspase-9 monomers(inactive)
Caspase-9 dimers(active)
Cell deathProcaspase-3 Caspase-3
Procaspase-7 Caspase-7
These caspases lead to the death and re-sorption of the cell
Apoptosome causes dimerizationof procaspase-9, creating active caspase-9 dimers
Caspase-9 catalyzes proteo-lytic activation of caspase-3and caspase-7
Cytochrome c
DNAdamage
Developmentalsignal Stress ROS
Apaf-1 (apoptosisprotease activating factor-1)
Apoptosome
Cytochrome cmoves to cytosol
Permeability transitionpore complex opens
Binding of cytochrome cand ATP induces Apaf-1 toform an apoptosome
ATP
Role of cytochrome c in apoptosis
![Page 35: Oxidative phosphorylation Biochemistry, 4 th edition, RH Garrett & CM Grisham,](https://reader034.vdocuments.us/reader034/viewer/2022050821/5681658d550346895dd85806/html5/thumbnails/35.jpg)
1. In mitochondria, hydride ions removed from substrates by NAD-linked dehydrogenasesdonate electrons to the respiratory (electron-transfer) chain, which transfers electrons to molecular O2 reducing it to H2O
2. The energy of electron flow is conserved by the concomitant pumping of protons across the membrane, producing an electrochemical gradient, the proton-motive force
3. Proton gradient provides the energy (in the form of the proton-motive force) for ATP synthesis from ADP and Pi by ATP synthase (FoF1 complex) in the inner membrane
4. ATP synthase carries out “rotational catalysis,” in which the flow of protons through Focauses each of three nucleotide-binding sites in F1 to cycle from (ADP + Pi)-bound to ATP-bound to empty conformations
5. Energy conserved in proton gradient can drive solute transport uphill across a membrane
6. In brown fat, electron transfer is uncoupled from ATP synthesis and the energy of fatty acid oxidation is dissipated as heat
7. Reactive oxygen species produced in mitochondria are inactivated by a set of protective enzymes that prevent oxidative stress
8. Mitochondrial cytochrome c, released into the cytosol can cause activation of caspasesand apoptosis