Ion Transporters Flashcards

1
Q

Which type of molecules can pass through the lipid bilayer?

A

Hydrophobic molecules such Oxygen, C02, N2, Benzene

Small, uncharged polar molecules such as H2O, Urea, Glycerol

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Which type of molecules can’t pass through the lipid bilayer?

A

The large free energy change that would be required for a small hydrophilic molecule or ion to traverse the hydrophobic core of the lipid bilayer make the transverse movement of hydrophilic molecules across an intact biological membrane a rare event. Thus, membranes act as permeability barriers to all charged and hydrophilic molecules.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What is a permeability coefficient?

A

the ease with which a membrane is permeable to a molecule

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What is passive transport dependent on?

A

Passive Transport is dependent on permeability and concentration gradient

Rate of passive transport increases linearly with increasing concentration gradient

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What roles do transport processes have?

A
  • Maintenance of ionic composition
  • Maintenance of intracellular pH
  • Regulation of cell volume
  • Regulating concentration of metabolic fuels and building blocks
  • The extrusion of waste products of metabolism and toxic substances
  • The generation of ion gradients necessary for the electrical excitability of nerve and muscle
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What is active or passive transport dependent on?

A
  • Concentration gradient
  • Membrane potential
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

How much energy do cells spend on active transport?

A

• Some cells spend up to 30 – 50 % of their ATP
on active transport

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Describe the concentration gradient for Sodium

A

145 out, 12mM in

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Describe the concentration gradient for Potassium

A

155mM in, 4mM out

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Describe the concentration gradient for Calcium

A

1 x 10-7M in, and 1.5mM out

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Describe the concentration gradient for chloride ions

A

123mM out, 4.2mm in

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Describe the action of the Na+-K+-ATPase Pump

A

3 sodium ions extruded, 2 potassium enter

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What is the importance of the sodium potassium pump?

A

Forms Na+ and K+ gradients:

– Necessary for electrical excitability

– (only contributes < - 5 mV to resting membrane potential)

Drives Secondary Active transport:

– Control of pH

– Regulation of cell volume and [Ca2+]

– Absorption of Na+ in epithelia

– Nutrient uptake, e.g. glucose from small intestine

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Describe the structure of the Na+-K+-ATPase Pump

A

-

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Describe how Ca2+ concentration in the cell is controlled

A
  • NCX (3 sodium in, for one calcium out. Low affinity, high capacity)
  • SERCA
  • PMCA (Proton moved in, Calcium ion moved out. ATP phosphorylated. System has a high affinity and low capacity)
  • Mitochondrial storage
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Describe the roles of the NCX exchanger

A

Electrogenic – current flows in the direction of the Na+ gradient

Role in expelling intracellular Ca2+ during cell recovery

Possible role in cell toxicity during ischaemia/reperfusion

Depolarised membrane potential reverses mode of operation (during ischaemia, ATP depleted, so sodium accumulates in cell. Causes calcium to move in which can cause toxicity)

17
Q

Describe the action of PMCA

18
Q

Describe how mitochondria can buffer intercellular calcium concentration

19
Q

Describe how calcium is taken up by the endoplasmic reticulum

20
Q

Describe the action of the Na+-H+ Exchanger

A

It is an acid extruder. It moves one sodium in, and one proton out. It regulates cell volume.

Amiloride inhibits and it is activated by growth factors

21
Q

Describe Na+-Glucose Co-Transport

22
Q

How is cellular pH controlled?

A

Sodium-Potassium ATPase sets up gradient for all transporters to work.

Na+-H+ Exchanger is an acid extruder

Na+-Cl-HC03-H+ (NBC) cotransporter is an acid extruder and alkali intruder

Na+-HCO3- cotransporter is an alkali intruder

HCO3-Cl- contransporter is an alkali extruder

23
Q

How is intracellular pH regulation co-ordinated?

A

pH is held at the set point. Any drift away from this pH is corrected by the increased activity of appropriate transporters

24
Q

How is cell volume regulated?

A

Transport of osmotically ‘active’ ions, e.g. Na+, K+, Cl- or organic osmolytes (amino acids). Water follows.

Cell swelling – extrude ions

Cell shrinking – influx ions

25
What are some mechanisms to resist cell swelling?
26
What are some mechanisms to resist cell shrinking?
27
Describe the role of transporters in diarrhoea
Infection e.g vibrio cholera causes PKA to irreverisbly activate CFTR. Chloride ion loss means excessive water in lumen, causing diarrhoea.
28
Why are erythrocytes more permeable to glucose?
They have no mitochondria so they need more efficient glucose transport
29
What is the difference between symport and antiport transporters?
Antiport transporters have molecules going in opposite directions, symport have them going the same.
30
How does Prozac work?
Prozac inhibits SERT, which normally functions to reuptake cleft serotonin. 5HT action increases leading to an improvement in symptoms. Side effects include sticky blood however.