Chapter 13- Lipids and Membranes Flashcards

1
Q

What are the 5 functions of biological membranes?

A
CITCE 
compartmentalisation
intercellular interaction
transport
communication
energy transduction
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Most membrane lipids are amphipathic, what does this mean?

A

They have a polar end and a non polar end.

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

What are the the simplest lipids, and what are they composed of?

A

fatty acids. A hydrocarbon chain with a carboxylic acid

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

What phases can lipids exist in?

A

crystal, fluid, gel?

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

Which enzyme catalyses lipid flip-flip- transverse diffusion?

A

flippase

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Name the 3 spontaneous assemblies that lipids assemble into?

A

micelle, bilayer, liposome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What are the driving forces for lipid self assembly?

A

entropic and enthalpies forces

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

What type of bonds hold lipid membranes?

A

non-covalent bonds.

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

What are 2 ways to avoid phase changes?

A
  1. Cholesterol/ sterols (long, staurated chain) or membranes would crystallise at physiological temp
  2. mitochondrial membrane doesn’t have cholesterol but has many phospholipids with double bonds- kinks= hard to pack and crystallzize= lower the melting point
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What 3 things influence membrane fluidity?

A
  1. fatty acid chain length
  2. saturated (double bonds- kinks)
  3. presence of sterols
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

what is the purpose of FRAP, and what does it stand for?

A

to measure lipid lateral diffusion. Flourescence recovery after photobleaching

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

Sterols are fluidity buffers, explain what they do at low and high temp?

A

@low temp- the prevent tail from interaction= ^ fluidity

@high temp- they restrict phospholipid movement= less fluid

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

How do amphibians adapt cold temperatures?

A

Add doubles and cholesterol.

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

What are lipid rafts?

A

Cholesterol + sphingolipids in the plasma membrane. they separate from glycerophospholipids.

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

Why are lipid rafts isolated?

A

because they are resistant to detergent solubilisation.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Why is it easy to pack lipid rafts?

A

The sphingolipid has no double bonds.

17
Q

What are caveolae?

A

invaginated lipid raft domain of plasma membranes.

18
Q

How do peripheral proteins associate to the membrane?

A

non covalently .

19
Q

How can you dislodge peripheral proteins ?

A

change in pH, extract with salt, or chelators.

20
Q

How can you dislodge integral proteins?

A

they must be solubilised with detergent.

21
Q

What is special about the picket fence model?

A

It restricts lateral diffusion of lipids, They have to stay within the fence.

22
Q

When try to isolate and study membrane proteins, explain ionic/ non-ionic detergents?

A

ionic detergents- denature proteins (SDS, CTAB, DOC)

non-ionic detergents, don’t denature proteins (TritonX-100, ocytylglucoside)

Purified proteins can be made into liposomes for study.

23
Q

Amphipathic detergents are used to solubilize integral proteins. Explain how it works?

A

The hydrophobiic parts simulate the lipids, the polar parts simulate the hydrophilic head and interact with water.

24
Q

What happens if the amphipathic detergent I removed from the integral protein solubilisation?

A

The proteins will aggregate and come out of solution.