Week 5- transport across membranes- Drewes Flashcards

1
Q

GLUT 1

GLUT 4

A

1- RBC

4- fat, muscle (including heart) and insulin sensitive

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2
Q

Na+/K+ pump

A

requires energy to transport 3 sodiums out of cell and 2 potassium into cell

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3
Q

Na+/glucose symporter

A

uses the energy of Na+ moving down its [ ] gradient to power glucose moving up its concentration gradient

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4
Q

how is ATP directly involved in the Na+/K+ shuttle

A

Na+ attaches to transporter ⇒ ATP P’s the transporter ⇒ conformational change allows Na+ to be moved to outside of the cell ⇒ 2 K+ go into the P’d transporter ⇒ the P is removed and a conformational change allows 2 K+ to come into the cell

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5
Q

Distinguish the unique features of the sodium-potassium ATPase.

A
  • use energy to pump 3 Na+ out and 2 K+ in (pumped against gradient)
    • this establishes the electrochemical gradient and resting membrane potential

-ATP is directly involved

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6
Q

Compare passive diffusion and facilitated diffusion.

A
  • passive diffusion
  • can freely move through the membrane
  • doesn’t require ATP
  • if you increase the [ ] you will increase the velocity (not saturable)
  • facilitated diffusion
  • doesn’t require ATP
  • if you increase the [ ] you don’t always increase the velocity (at some point you will reach a max velocity- when all the proteins are full) (saturable)
  • examples: pores, gated channels, carrier proteins
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7
Q

Calculate the free energy change associated with transport

A
-ΔG= movement down a [ ] gradient
\+ΔG= movement against a [ ] gradient
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8
Q

drug that inhibit Na+ K+ channel

A

digotoxin

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9
Q

Compare primary versus secondary active transport.

A
  • Primary → directly hydrolyzes ATP

- Secondary → uses the energy of another molecule to move against concentration gradient

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10
Q

Describe the mechanism of ionophores.

A

2 proteins that come together in the membrane to form a pore for ions to transport through. This is typically used in drugs as an antibacterial or antiviral.

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11
Q

Describe ligand-activated ion channels

A

Ligand-activated ion channel has a binding site for ligand (drug or other substrate), and when the ligand binds to the receptor, the channel opens and allows for flow of ions

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12
Q

Distinguish the differences between channels and pumps.

A

Channels → specific for 1 molecule, can be open or closed, molecules move down concentration gradient
Pumps → specific for molecules, use energy to power, molecules move against their concentration gradient

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13
Q

normal function of CFTR

A

allow Cl- transport across the cell membrane AND to regulate transport of other ions via interactions with their transport proteins

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14
Q

diagnosis for cystic fibrosis

A

skin will be salty

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15
Q

Postulate the mechanism for opening voltage-sensitive channels.

A

Leak channels can cause change in voltage of membrane potential, which can trigger voltage sensitive channels to open

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16
Q

Describe why ion channels are considered allosteric proteins

A

When an ion binds to the channel, it can cause a conformational change that allows the channel to open.

17
Q

Suggest how channels can be selective

A

Depending on the charge of amino acids that line the channel, you can get selectivity via interactions between ion and the amino acids

18
Q

Compare in molecular terms a Na+, K+, and Ca2+ channel

A

Na+ and Ca++: very similar- 4 repeats of a 6 transmembrane domain; voltage gated
-K+: one 6 transmembrane seq.; ethyl groups cause plugging of the channel

19
Q

cystic fibrosis

A

cystic fibrosis: mutation in the CFTR gene (loss of a phenylalanine at F508)

  • this mutation causes defect in Cl- channels: doesn’t allow Cl- to be reabsorbed so it all goes to the surface (why ppl will taste salty that have this)
  • have this problem in the lungs as well: Cl- wont allow mucus to clear properly ⇒ becomes a breeding ground for bacteria ⇒ people with this die of bacterial infections