8. Carrier-mediated transport Flashcards

1
Q

how can valinomycin be used as a antibiotic

A

makes the membrane leaky to potassium

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2
Q

valinomycin:

  • what is the structure
  • where does K+ bind
A

ring structure due to trimeric repeating cycle

K+ binds in the centre of the ring in a hydrophilic pocket

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3
Q

what is the mechanism of transport for valinomycin

A
  1. valinomycin binds to potassium
  2. potassium is dehydrated so it can freely diffuse
  3. leaves the membrane and become hydrated again
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4
Q

what are the kinetic properties of carriers (3)

A
  1. binding of substrate from outside and formation of carrier-substrate complex
  2. re-orientation of the carrier-substrate complex to align the binding site to the inside
  3. empty carrier re-orientates itself to align its binding site with the outside
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5
Q

define Vmax

A

the maximum possible rate of the reaction at that enzyme concentration

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6
Q

define Km

A

the substrate concentration at which the velocity of the reaction is HALF Vmax

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7
Q

what does a low Km indicate

A

a high affinity of the enzyme for the substrate

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8
Q

what does a high Km indicate

A

indicates low enzyme affinity for a substrate = a higher substrate conc. would fix this

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9
Q

give an example of an inophore

A

valinomycin

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10
Q

define inophore

A

a small lipid molecule that can bind a specific ion

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11
Q

describe how glucose is transported across the membrane using GLUT2

A
  1. glucose binding site faces outwards and binds glucose

substrate binding = extra contact = high affinity between TMS 7 & 1

  1. = conformational change, orientates the binding site inwards
  2. glucose dissociates
  3. GLUT2 re-orientates to expose the binding site to the outside
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12
Q

what are neurotransmitter sodium symporters involved in

A

removing dopamine from the synaptic cleft

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13
Q

how do sodium symporters work to remove dopamine

A

sodium and chloride is required to drive transport of dopamine against its concentration gradient

removing dopamine from the synaptic cleft

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14
Q

what drugs target sodium symporters - what is the effect

A

anti-depressant drugs

  • increasing the amount of dopamine present in the synaptic cleft
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15
Q

what is the alternate access model

A

hairpin loop is open and outward facing = binding occurs

then the inward facing binding site opens and substrates are released

BOTH GATES ARE NEVER OPEN AT THE SAME TIME

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16
Q

what is the structure of neurotransmitter sodium symporters

A

two hairpin loops form gates (alternate access model)

8 TMS

17
Q

what is the difference between GLUT1 AND GLUT2

A

GLUT1 -main transporter of glucose to the brain (via the blood brain barrier)
GLUT2 - main transporter of glucose between the liver and the blood

18
Q

the disregulation of which GLUT transporter leads to diabetes

A

GLUT2

19
Q

name 2 examples of physiologically important carriers

A

sodium-coupled sugar transport in mammalian cells

sodium-calcium antiporter in cardiac cell membranes

20
Q

how does Na+-coupled sugar transport work in mammalian cells

A

uses sodium/potassium ATPase to transport glucose against its concentration gradient via GLUT2 symporter

21
Q

why is Na+Ca2+ antiporters important in cardiac muscle cells

A

maintains low cytosolic calcium - which allows diastole following contraction

22
Q

how do Na+Ca2+ antiporters work in cardiac muscle cells

A

Na+/K+ ATPase which maintains sodium gradient - enabling calcium efflux via antiporter

23
Q

what is the benefit of coupling sodium transport to glucose transport

A

free energy produced from moving NA+ down its conc gradient, permits the transporter to move glucose against its conc gradient (energetically costly)

24
Q

how does sodium-calcium antiporters work to remove calcium from the heart muscle following systole

A

Na/K+ pump maintains Na+ gradient

antiporter brings 3 Na+ into the cytosol and removes 1 calcium molecule per rotation - this uses the free energy favouring the efflux of calcium