Lecture 17 + 18, Transport Proteins (Ford) Flashcards

(38 cards)

1
Q

List the 2 methods to cross a membrane.

A

Active or passive transport

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2
Q

Describe passive transport.

A

No energy needed, solute travels down concentration gradient

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3
Q

Describe active transport.

A

Coupled to ATP hydrolysis, solute travels against concentration gradient

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4
Q

What are the 3 general modes of transport across a membrane?

A

Antiport, synport, uniport

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5
Q

List the 3 general categories of transporters.

A

Pumps, carriers, channels

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6
Q

Describe pumps.

A

Perform primary active transport

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7
Q

Describe carriers.

A

Traverse membrane without needing extra energy

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8
Q

Describe channels.

A

Used in passive transport

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9
Q

T or F: P-type pumps phosphorylate themselves.

A

True.

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10
Q

T or F: V-type proton pumps make ATP.

A

False. V-type proton pumps use ATP, while F-type ATP synthase makes ATP.

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11
Q

What are the 4 domains of P-type ATPases?

A

Transmembrane domain, actuator domain, nucleotide binding domain, phosphorylation domain

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12
Q

T or F: The transmembrane domain of a P-type ATPase spans the lipid bilayer.

A

True.

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13
Q

Describe the actuator domain of a P-type ATPase.

A

Links cytosolic domains to the transmembrane domain

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14
Q

Which domain of the P-type ATPase binds ATP?

A

Nucleotide binding domain

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15
Q

Which domain of the P-type ATPase accepts the phosphate from ATP?

A

Phosphorylation domain

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16
Q

Outline the action of SERCA.

A
  1. E1 unphosphorylated, Ca++ ions bound
  2. ATP binds, Ca++ ions trapped
  3. ATP hydrolysis, self phosphorylation
  4. Eversion to E2, Ca++ ions released
  5. Release of Pi
  6. Eversion to E1
17
Q

T or F: The E1 state of SERCA is open to the outside.

A

False. The E1 state of SERCA is open to the inside.

18
Q

Outline the action of the Na++/K+ pump.

A
  1. E1, Na+ ions bound, ATP bound
  2. Na+ ions trapped
  3. ATP hydrolysis, self phosphorylation
  4. Eversion to E2, Na+ ions released
  5. Binding of K+
  6. K+ ions trapped, release of Pi, ATP rebinding
  7. Eversion to E1
  8. Release of K+
19
Q

Describe an application of primary active transport.

A

Digitalis and ouabain both lock the Na+/K+ pump in the E2 conformation.

20
Q

Outline the action of an ABC transporter.

A
  1. Empty transporter
  2. Small molecule binds and is trapped; ATP binding site affinity increases
  3. 2 ATPs bind causing eversion
  4. Small molecule is released
  5. ATP hydrolysis and release
21
Q

How is secondary active transport carried out?

A

After primary active transport creates a gradient, a passive channel or carrier allows ions/molecules to fall back down the gradient with a high value stowaway.

22
Q

Outline the secondary active transport action of lactose permease.

A
  1. Empty carrier, H+ binds and increases affinity for lactose
  2. Lactose binds
  3. Eversion
  4. Lactose released
  5. Deprotonation
  6. Eversion
23
Q

T or F: By definition, all secondary transporters are antiporters.

A

False. By definition, all secondary transporters are symporters.

24
Q

List the factors affecting diffusion rates.

A
  1. Magnitude of the concentration gradient
  2. Size of the molecule
  3. Surface area:volume ratio (shape)
  4. Temperature
  5. Density of solvent
  6. Solubility of solute
  7. Distance to destination
25
How will a larger concentration gradient affect diffusion rate?
Faster
26
How will a smaller molecule affect diffusion rate?
Faster
27
How will a higher surface area:volume ratio affect diffusion rate?
Faster
28
How will a lower temperature affect diffusion rate?
Slower
29
How will a solvent with high density affect diffusion rate?
Slower
30
How will a nonpolar solute affect diffusion rate?
Soluble
31
How will a longer distance to the destination affect diffusion rate?
Slower
32
What are 2 important pieces of an ion channel?
1. Selectivity filter | 2. Gate
33
What does movement result from in a bacterial K+ channel?
Results form electrostatic repulsion
34
What are the 3 ways to gate a channel?
1. Voltage 2. Ligand 3. Stress
35
Describe the 5 ion channels that work together to contact the muscles.
1. Depolarization opens voltage-gated Ca++ channels 2. Exocytosed acetylcholine opens ligand-gated Na+ channels 3. Local depolarization opens adjacent voltage-gated Na+ channels 4. As the depolarization spreads, voltage gated Ca++ channels open 5. Coupled Ca++ release channels embedded in SR open
36
What are the various proteins that facilitate diffusion?
Ion channels
37
Describe gap junctions.
Channel, allow cytoplasm sharing, no specificity filter
38
Describe aquaporins.
Channel, let water but not ions through