8. Carrier-mediated transport Flashcards
how can valinomycin be used as a antibiotic
makes the membrane leaky to potassium
valinomycin:
- what is the structure
- where does K+ bind
ring structure due to trimeric repeating cycle
K+ binds in the centre of the ring in a hydrophilic pocket
what is the mechanism of transport for valinomycin
- valinomycin binds to potassium
- potassium is dehydrated so it can freely diffuse
- leaves the membrane and become hydrated again
what are the kinetic properties of carriers (3)
- binding of substrate from outside and formation of carrier-substrate complex
- re-orientation of the carrier-substrate complex to align the binding site to the inside
- empty carrier re-orientates itself to align its binding site with the outside
define Vmax
the maximum possible rate of the reaction at that enzyme concentration
define Km
the substrate concentration at which the velocity of the reaction is HALF Vmax
what does a low Km indicate
a high affinity of the enzyme for the substrate
what does a high Km indicate
indicates low enzyme affinity for a substrate = a higher substrate conc. would fix this
give an example of an inophore
valinomycin
define inophore
a small lipid molecule that can bind a specific ion
describe how glucose is transported across the membrane using GLUT2
- glucose binding site faces outwards and binds glucose
substrate binding = extra contact = high affinity between TMS 7 & 1
- = conformational change, orientates the binding site inwards
- glucose dissociates
- GLUT2 re-orientates to expose the binding site to the outside
what are neurotransmitter sodium symporters involved in
removing dopamine from the synaptic cleft
how do sodium symporters work to remove dopamine
sodium and chloride is required to drive transport of dopamine against its concentration gradient
removing dopamine from the synaptic cleft
what drugs target sodium symporters - what is the effect
anti-depressant drugs
- increasing the amount of dopamine present in the synaptic cleft
what is the alternate access model
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