mueller electron transport Flashcards

1
Q

What is the lipid and protein composition of the outer mitochondrial membrane?

A

50% lipid and 50% protein

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2
Q

What is the protein and lipid composition of the inner membrane?

A

80% protein and 20% lipid

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3
Q

What is the one TCA cycle enzyme that is not soluble?

A

succinate dehydrogenase

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4
Q

What proteins do mitochondrial genes encode?

A

ATP synthase. Complexes I, III, IV

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5
Q

What are the reduced substrates for ETC?

A

NADH and succinate

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6
Q

What are the major dehydrogenases that funnel electrons to the ETC?

A
  1. succinate dehydrogenase
  2. NADH dehydrogenase
  3. fatty acyl-CoA dehydrogenase
  4. Glycerol-3-phosphate dehydrogenase
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7
Q

What is different about the cytochromes iron compared to hemeglobin or myoglobin?

A

cytochrome iron can undergo changes in its ionization state

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8
Q

What dehydrogenase contain FAD?

A

succinate, fatty acyl and glycerol-3-phosphate

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9
Q

WHat dehydrogenases contain FMN?

A

NADH

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10
Q

What is the purpose of CoQ?

A

shuttle electrons from various dehydrogenaes to complex III

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11
Q

What are complex I and II?

A

I. NADH - CoQ reductase

II. Succinate CoQ reductase

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12
Q

What reaction to complex II catalyze?

A

succinate to fumarate

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13
Q

What are complex III and IV?

A

III. Cytochrome c reductase

IV. cytochrome c oxygenase

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14
Q

What are two important inhibitors of complex IV?

A

cyanide and CO

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15
Q

What other metal ion does complex IV contain?

A

copper

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16
Q

What complex does not produce enough energy by itself to produce ATP?

A

complex II

17
Q

What are the three sites of proton extrusion in ETC?

A

Complexes I, III, IV

18
Q

How many ATP per NADH?

19
Q

How many ATP per FADH2

20
Q

What is the role of Fo?

A

transmembrane protein that forms a proton channel

21
Q

What is F1?

A

catalytic moiety that is involved in the actual synthesis of ATP from ADP.

22
Q

How does 2,4-DNP uncouple ETS?

A

by physically carrying protons from the periplasmic space and back into the mitochondrial matrix

23
Q

How does ATP leave matrix?

A

via adenine nucleotide translocase

24
Q

How does atractyloside inhibit electron flow?

A

via inhibition of adenine nucleotide translocase

25
What component of ETS is implicated in LHON?
Complex I
26
What two disorders include point mutations in genes encoding tRNAs?
MARRF and MELAS
27
What do MERRF and MELAS stand for?
myoclonic epilepsy and ragged red fibers mitochondrial encephalopathy, lactic acidosis, stroke-like activity
28
The activity of what ETS complex is implicated in MERRF?
cytochrome oxidase
29
What causes MELAS?
leucine tRNA mutation
30
What is administered to combat the effects of cyanide?
sodium thiosulfate
31
What does LHON often present with?
sudden onset blindness in young adults
32
What tRNA is mutated in MELAS?
leucine tRNA