OxPhos reg/ Agbas Flashcards

Disrupt Time/space continuum

1
Q

What are the three goals of OxPhos?

A
  • Transfer electrons
  • Establish a proton gradient
  • Synthesize ATP
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2
Q

What is the chemiosmotic hypothesis?

A

Energy is generated from creating a proton gradient

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3
Q

What two forces constitute the pmf which drives ATP synthesis?

A
  • pH gradient

- Membrane potential

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4
Q

What are the 3 postulates of the chemiosmotic theory?

A
  1. mETC translocates e- across inner mm from one rspiratory ecc complex to another
  2. ATP Synthase uses pmf to drive phosphorylation of ADP
  3. IMM is impermeable to H+/OH-
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5
Q

Describe the basic structure of ATP synthase.

A
  • Transmembrane
  • Ball and stick shape w/ two subunits
  • F0 “stick” intramembrane subunit is proton channel
  • F1 subunit is “ball” and contains catalytic domain
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6
Q

Describe the structure of the F1 subunit of ATP Synthase

A
  • 5 subunits; a3, B3, y, Delta, and e
  • a/B hexameric ring
  • a/B bind nucleotides, ONLY B CATALYTIC
  • y has long helical coil extending into hexamer
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7
Q

What is important regarding the formation of ATP Synthase?

A
  • Form dimers -> form oligomers
  • Structure stabilizes rotational forces
  • Maintains curvature in inner membrane
  • Cristae formed allow close proximity to H+ gradient
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8
Q

Why do cristae display a folded structure?

A. To increase SA
B. Increase TCA cycle
C. Form efficient proton gradient in groove
D. Increase ETC reactions

A

C. Form efficient proton gradient in groove

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9
Q

How many Kcal of energy used per mole of ATP formed?

A

7.3 Kcal/Mol

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10
Q

What is oligomycin?

A

ATPase inhibitor (F0)

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11
Q

What constitutes pmf?

A. pH gradient
B. Membrane potential
C. ATP production rate
D. pH gradient and membrane potential
E. ADP concentration
A

D. pH gradient and membrane potential

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12
Q

What is ATP-ADP translocase?

A
  • ATP/ADP not permeable across membrane
  • Carries ATP/ADP through outer and inner mito-membranes
  • Complex VI
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13
Q

How many H+ are needed for ATP synthesis and translocation?

A

4 H+
3 -> Synthesis
1 -> translocation

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14
Q

What are the two shuttle systems for NADH to cross mitochondrial membrane?

A

Malate -> aspartate shuttle: Oxaloacetate reduced and gets converted to malate and shuttled into mitochondria. Malate transported back as a-ketoglutarate via conversion of aspartate

Glycerophosphate -> FADH2 reduction of Glyceral3P which enters and mitochondria,

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15
Q

What is the organ location, generated substrate, and ETC entrance for Malate-aspartate shuttle?

A
  • Heart, Liver, and kidneys
  • Generates NADH in matrix
  • Enters ETC at Complex I
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16
Q

What is the organ location, generated substrate, and ETC entrance for Glycerophosphate shuttle?

A
  • muscle and brain
  • generates FADH2 in inner Mitomembrane
  • FADH2 joins at CoQ
17
Q

What molecule is regulated by respiratory control (acceptor control)?

A

ADP

18
Q

Which of the following factors governs the pmf in intact mitochondria?

A. Standard redox potential of intermediates
B. ATP production rate
C. Membrane potential and pH gradient
D. Proton gradient formaiton in intermembrane space

A

D. Proton gradient formaiton in intermembrane space

19
Q

What are the complex I inhibitors?

A

Amytal
Rotenone
Myxothiazol
Piericidin A

20
Q

What is/are the complex II inhibitor(s)?

A

Malonate

21
Q

What is/are the complex II inhibitor(s)?

A

Antimycin

22
Q

What is/are the Complex IV inhibitor(S)?

A

CO
Cyanide
H2S

23
Q

How can some organisms generate heat with low ATP synthesis?

A
  • Brown adipose tissue is able to uncouple OxPhos and ATP synthesis.
  • IMM contains uncoupling protein (UCP 1 or thermogenin) which transfers protons from cytoplasm to matric
  • Energy converted to heat instead of ATP