3.5 - Protein Trafficking from Golgi Flashcards

1
Q

types of secretion from golgi (2)

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

constitutive secretion

A

vesicles move directly from golgi to plasma membrane

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

regulated secretion

A

fusion of vesicles with plasma membrane depends on signal

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

regulated secretion example

A

insulin secretion in beta cells of pancreas

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

how is insulin secretion in beta cells of pancreas triggered by rise in blood glucose? (4)

A
  1. uptake of glucose by GLUT2 transporter
  2. glycolysis leads to rise in ATP:ADP ratio
  3. inactivates K+ channel, depolarising membrane causing Ca2+ channels to open
  4. rise in Ca2+ causes insulin release from vesicles (SNAREs activated by Ca2+)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

lysosome

A

membrane-bound sacs of hydrolytic enzymes

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

examples of lysosomes digesting extracellular material and worn out cellular organelles (3)

A
  1. endocytosis
  2. phagocytosis
  3. autophagy
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

how do lysosomes maintain a low pH?

A

ATP-driven pump of H+ into lumen

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

why does the lysosome lumen have a low pH?

A

collection of hydrolytic enzymes active in acidic conditions

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

purpose of transporters in lysosome membrane

A

transfer sugars, amino acids, nucleotides to cytoplasm

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

why are lysosomes made as inactive precursors with an extra peptide

A

because theyre dangerous?

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

lysosome activation

A

extra peptide cleaved off

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

what recognise lysosomal proteins in cis-golgi?

A

sorting patch

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

how does sorting patch recognise recognise lysosomal proteins in cis-golgi? (2)

A
  1. add P-GIcNAc to mannose on N-linked sugar
  2. then remove GIcNAc - mannose-6-phosphate
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

role of dynamin in vesicle formation (pinching off)

A

dynamin polymerises around neck (vesicle separates from membrane)

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

what drives conformational change in dynamin (pinching off)

A

GTP hydrolysis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

examples of cell surface to lysosome endocytosis (2)

A
  1. phagocytosis
  2. receptor-mediated endocytosis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

endosome

A

first destination for endocytic vesicles

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

role of endosome

A

sorting station for endocytic pathway (some molecules sent to lysosome some recycled)

20
Q

how does endosome determine where vesicles are next transported?

A

depends whether ligand and receptor within vesicle membrane endocytosed stay associated

21
Q

endosome transport if receptor bound for recycling?

A

vesicle will go there

22
Q

endosome transport if receptor bound for transfer to other side of cell

A

they will transcytose

23
Q

endosome transport if receptor and ligand do not remain bound due to acidic nature of endosome

A

will go to lysosome for degradation

24
Q

lipoprotein particle

A

‘packages’ of lipids and cholesterol bound by apoprotein B-100

25
low density lipoprotein (LDL)
'bad cholesterol'
26
LDL receptor
transmembrane protein
27
LDL receptor role (4)
1. binds to LDL outside cell and adaptins inside cell 2. adaptins bind clathrin 3. LDL internalised in coated vesicles 4. delivered to lysosomes
28
what can a mutation in the LDL receptor cause?
no binding to adaptin
29
aim of transferrin receptor
get iron into cell
30
components of transferrin receptor (3)
1. Fe3+ ions 2. transferrin 3. transferrin receptor
31
iron-dependant binding in transferrin receptor
transferrin to receptor
32
pH-dependant binding in transferrin receptor
Fe3+ to transferrin, transferrin to receptor
33
pH of endosomes
acidic
34
EGF receptor
'epidermal' growth factor receptor
35
EGF receptor role (4)
1. EGF binds 2. receptor becomes dimer 3. tyrosine kinase phosphorylates itself 4. cells proliferate
36
epidermal growth factor
'on' switch for cell proliferation
37
'off' switch for cell proliferation
endocytosis of EGF and receptor to lysosome
38
familial hypercholesterolaemia (3)
1. lots of LDL and receptor 2. receptor spread all over cell surface, not in clathrin coated pits 3. mutation Y in cytoplasmic region impacting adaptin binding signal
39
mannose-6-phosphate disease example
mucolipidosis II
40
LDL receptor disease example
familial hypercholesterolaemia
41
mucolipidosis II (2)
1. lysosomal enzymes secreted into bloodstream 2. defect in GIcNAc phosphotransferase
42
protein involved in cystic fibrosis
ATP-dependant chloride channel
43
most common mutation causing cystic fibrosis
∆F508
44
result of mutation causing cystic fibrosis
ATP-dependant chloride channel protein unable to stay in first place
45
problem with protein folding involved in cystic fibrosis
cytoplasmic chaperones stuck on and cant enter COPII vesicles (most of protein on cytoplasmic side)