10: Ox Phos Flashcards

1
Q

Three goals of ox phos

A
  1. Transfer electrons from NADH and FADH2 -> O2
  2. Establish proton gradient across inner mito membrane
  3. Synthesize ATP
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2
Q

Standard redox potential (Eo’)

A

Affinity for electrons (inversely proportional to delta G)

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3
Q

Chemiosmotic theory

A

Electron transfer through respiratory chain leads to pumping of H from matrix to inner-mito space

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4
Q

Proton motive force (pmf) two components

A

PH gradient, membrane potential

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5
Q

What generates most ATP in the cell?

A

Oxphos

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6
Q

Three main sources of NADH

A
  1. TCA
  2. Pyruvate dehydrogenase
  3. Ketone body oxidation
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7
Q

Three main sources of FADH2

A
  1. Complex II
  2. Glycerol phosphate shuttle
  3. FaCoA dehydrogenase
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8
Q

Which respiratory chain complex is not coded by any mito DNA?

A

Complex II

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9
Q

What treatment can overcome rotenone poisoning?

A

Vitamin K3 (menadione)

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10
Q

Side affects of nucleoside analogue treatments like AZT, AraC, and ddC

A

Fatigue, lactic acidosis, myopathy, cardiac dysfunction, hepatic failure

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11
Q

F0 and F1 subunits of ATP synthase

A

F0: membrane-spanning channel
F1: where ATP synthesis occurs

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12
Q

Forming 1 ATP requires passage of how many H ions?

A

3

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13
Q

Uncoupling of respiratory chain

A

H ions leak through UCP1 (thermogenin), disrupting proton gradient -> energy released as heat

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14
Q

How is thermogenesis in brown tissue started

A

Brain senses cold -> symp stimulation to brown adipose -> TAGs broken into FAs -> FAs activate UCP1

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15
Q

Common mitochondrial free radical

A

Ubiquinone radical (partially reduced ubiquinone during e transfer)

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16
Q

What do superoxide dismutases do?

A

Catalyze O2 superoxide + 2H _> O2 + H2O

17
Q

SOD1

A

Cu/Zn SOD; cytosolic

18
Q

SOD2

A

Mn/Zn SOD; mitochondrial

19
Q

What enzyme catalyzes hydrogen peroxide into O2 and water?

A

Catalase

20
Q

Name three common antioxidants

A

Glutathione, vitamin E, vitamin C

21
Q

Cytochrome P450 superfamily

A

An e- transport system in the ER that uses NADPH

22
Q

How does hypoxia in MIs cause lactic acidosis?

A

Lack of O2 -> decreased respiratory chian activity -> cells depend on glycolysis for energy -> lactic acidosis

23
Q

First discovered mito disease

A

Luft’s disease

24
Q

Luft’s disease symptoms

A

Perspiration, marked fluid intake with normal urine volume high caloric intake, weakness

25
Q

Primary and secondary causes of mitochondrial diseases

A

Primary: defect in DNA (mito or nuclear)
Secondary: ischemia, perfusion, CV disease, renal failure, drugs, aging, alcohol, smoking, etc.