Membrane trafficking Flashcards

1
Q

Cell polarity

A

Differences at each end
(eg. apical and basolateral domain)

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2
Q

What can polarized cells do or have?

A
  1. they have different function at different cell regions
  2. they define the inside v/s the outside
  3. transmit signals from one end to the other
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3
Q

What does membrane trafficking do?

A

Sends different proteins to different domains

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4
Q

Two main types of membrane trafficking

A
  1. exocytosis directly to target domain
  2. exocytosis to any domain and then endocytosis followed by recycling to target domain
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4
Q

Key concepts in secretory pathway

A
  1. Some trafficking routes are polarized (ER to Golgi to PM)
  2. Proteins are organized at sorting stating (trans golgi network)
  3. Different routes are balanced by retrieval pathways (ER retrieval from golgi)
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5
Q

What pathway is the default pathway?

A

Constitutive secretion

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6
Q

What is NOT required for constitutive secretion?

A

Specific signals

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7
Q

What do clathrin-coated vesicles do?

A

They can return the membrane to the Golgi, this shrinks the vesicle and makes cargo more concentrated.

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8
Q

Regulated secretion

A

Here membranes are fully formed but only fuse with the plasmam membrane when a signal is recieved.

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9
Q

Example of regulated secretion

A

Mast cell storing histamine

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10
Q

Ways in which regulated secretion can deliver extra membrane material

A
  1. cytokinesis
  2. phagocytosis
  3. plasma membrane repair
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11
Q

3 options that endocytosed proteins have

A
  1. recycling to the same domain of the plasma membrane
  2. transcytosis to other domain of plasma membrane
  3. degradation in the lysosome
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12
Q

3 types of membrane changes during vesicle trafficking

A
  1. vesicle forms from the donor membrane into the cytoplasm
  2. vesicle fusion: vesicle merges with a target membrane
  3. vesicle forms from a donor membrane away from the cytoplasm
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13
Q

What coat can mediate vesicle formation into the cytoplasm?

A

Clathrin

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14
Q

What helps vesicle fusion?

A

SNARES
Both t and v SNARES
they must be on opposite membrane

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15
Q

ESCRT proteins

A

pinch
They form vesicles away from the cytoplasm (into the lumen or extracellular space)
Vesicle formation machinery is in the cytoplasm.

16
Q

Phosphoinositides

A

they label different membrane domains

17
Q

where are phosphoinositides found?

A

different PIPs are found at different subcellular locations

18
Q

Basic structure of PIP

A

inositol sugar, phosphate group (C1), glycerol and lipids

19
Q

Where can phosphoinositides phosphorylted?

A

They are always phosphorylated at C1 but they can also be phosphorylated at C 3,4 and 5.

20
Q

What are PIPS interconverted by?

A

PIP kinase (adds phosphate) and PIP phosphotase (removes phosphate)
Not all PIPs can be directly interconverted

21
Q

What proteins bind to PIP, cargo and clathrin

A

adaptor proteins

22
Q

which PIP targets clathrin coat assembly?

A

PI(4.5)P2

23
Q

RAB GTPAses

A

they are molecular switched that can direct vesicles
GEF exchanges GDP for GTP
GAP activates GTPase

24
Q

How do Rabs and PIPs combine to give membrane different identities?

A
  1. Rab 5 GTP recruits PI 3 - kinase
  2. PI3P can recruit RAB 5 GEF
  3. More Rab 5 GEF makes more active Rab 5 GTP
25
Q

How do Rabs and PIPs combine to give membrane different identities? process

A

With a rab 5 GEF, rab 5 will release the GDP and bind to GTP, GDI leaves once this exchange happens, Rab 5 is on - lipid tether is exposed and it can insert into membrane.

26
Q

What work together in vesicle targetting and fusion?

A

Rabs and SNAREs