Chapter 13: Intracellular Membrane Traffic Flashcards

1
Q

What important concept is maintained during intracellular membrane trafficking?

A

topological equivalence

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2
Q

What are the 3 types of intracellular membrane trafficking pathways?

A
  1. endocytic
  2. biosynthetic-secretory
  3. retrieval
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3
Q

What pathway involves absorbing extracellular material into the cell?

A

endocytic pathway

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4
Q

what pathway involves the transfer of material from the nuclear envelope/ER to the Golgi, vesicles, or outside of the cell?

A

Biosynthetic-secretory pathway

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5
Q

what pathway involves the transfer of cell material from other pathways back to the ER?

A

retrieval pathway

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6
Q

The endocytic pathway utilizes what protein to aid in intracellular transport?

A

clathrin

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7
Q

Retrograde transport utilizes what protein to aid in intracellular transport?

A

COP1

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8
Q

The synthesis and secretory transport utilize what protein to aid in intracellular transport?

A

COP2 (+clathrin)

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9
Q

Cholesterol receptor-mediated endocytosis is typically regulated by what protein/transport type?

A

Clathrin; endocytic pathway

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10
Q

In what scenario would a cell use COP1 proteins for intracellular membrane transport?

A

To return proteins that have been mistakenly transported to certain organelles; retrieval/retrograde pathway

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11
Q

COP2 proteins are found in what portion of the cell? What is their function?

A

ER; transport to topologically equivalent spaces

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12
Q

What are the 4 basic steps of clathrin-based vesicle formation?

A
  1. coat assembly and cargo selection
  2. bud formation
  3. vesicle formation
  4. uncoating
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13
Q

This particular protein attaches to cargo receptors to allow for the association of the clathrin triskeleton

A

adaptor protein

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14
Q

these proteins aid in the vesicular formation of a clathrin-coated membrane

A

membrane-bending and fissure proteins

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15
Q

On what side of the membrane does the clathrin triskeleton bind to?

A

cytosolic

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16
Q

What phenomenon induces the budding and fission of a clathrin-coated vesicle?

A

clathrin triskeleton bending

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17
Q

This is a vesicular formation/fission protein that has contractile function driven by GTP

A

dynamin helix

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18
Q

What are the three steps of directed traffic endocytosis?

A
  1. tethering of vesicle via Rab-GTP
  2. docking on membrane via t-snare/v-snare interaction
  3. Fusion of vesicle into cell (and release of Rab-GTP)
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19
Q

What is required of a protein for COP2 ER transport of it to occur?

A

exit signal corresponding to cargo receptor

20
Q

What are the 2 possible fates of a resident ER protein?

A
  1. retention signal prevents removal – remains in ER lumen
  2. protein is taken up by vesicle formation – diffused out of ER lumen (to topologically equivalent spaces)
21
Q

These are membrane-bound regions between the ER and cis-Golgi network where retrieval transport can occur

A

vesicular tubular cluster

22
Q

What are the 3 cisternae of the Golgi stack?

A
  1. cis
  2. medial
  3. trans
23
Q

What are the 3 total regions of the Golgi apparatus?

A
  1. cis Golgi network
  2. Golgi stack
  3. trans Golgi network (TGN)
24
Q

The cis Golgi network is responsible for what?

A

Sorting & phosphorylation of oligosaccarides

25
The cis cisternae of the Golgi stack is responsible for what?
removal of Man
26
what is the function of the medial cisterna of the Golgi stack?
removal of Man & addition of GlcNAc
27
what is the function of the trans cisterna of the Golgi stack?
addition of Gal & addition of NANA
28
what is the function of the trans cisterna of the Golgi stack?
addition of Gal & addition of NANA
29
what is the function of the TGN?
sorting & sulfation of tyrosines and carbohydrates
30
what are the 3 major fates of TGN sorting?
1. lysosome 2. plasma membrane 3. secretory vesicle
31
what are the three possible sources of a lysosome?
1. phagosome 2. late endosome 3. autophagosome
32
this vesicular structure is responsible for digesting the cell's own structures (i.e. mitochondrion, chloroplasts)
autophagosome
33
this vesicular structure is formed via the endocytosis of large, foreign structures (i.e. bacterium)
phagosome
34
this vesicular structure is formed via the endocytosis of smaller structures and can mature into another structure when introduced to a product of macropinocytosis
early endosome
35
the addition of the products of macropinocytosis to the products of endocytosis results in what structure?
late endosome
36
What are the 7 basic steps (and the locations where they occur) of lysosomal hydrolase transport to endosomes?
1. Addition of P-GlcNAc (cis Golgi network) 2. uncover M6P signal (Golgi stack) 3. Binding to M6P receptor (TGN) 4. Transport to endosome (transport vesicle) 5. Dissociation @ acidic pH (endosome) 6. Removal of phosphate (endosome) 7. Receptor retrieval (transport vesicle)
37
What is essential in providing the acidic endosomal environment to ensure the dissociation of lysosomal hydrolase precursor from the M6P receptor?
V-type ATP proton pump
38
Where is the dysfunction located at in I-cell disease?
lack of M6P signal (no mannose phosphorylation) on lysosomal hydrolase precursor
39
What is the result of I-cell disease?
insufficient endosomal hydrolase activity--largely effects nervous system
40
What are the 8 basic steps of cholesterol delivery via LDLs?
1. LDL binding to extracellular receptors 2. formation of clathrin coat 3. uncoating 4. fusion into Golgi network 5. LDL transfer to late endosome (& retrieval of LDL receptor) 6. late endosome --> endolysosome 7. release of free cholesterol via hydrolytic enzymes 8. recycling of lysosome
41
this secretory pathway is used to transport/release membrane lipids or soluble proteins in an unregulated membrane fusion; this is often the default for molecules with no target info
constitutive secretory pathway
42
this secretory pathway occurs in response to the activity of an extracellular receptor (via hormones/NTMs) to induce regulated membrane fusion
regulated secretory pathway
43
In what cells to secretory vesicles form?
only in cells that perform excretion functions (i.e. toxicant removal)
44
What is the default fate/location of a protein translocated into the ER lumen (only contains an ER localizing signal)?
extracellular space
45
What is the default fate/location of proteins synthesized via cytosolic transcription?
usually mitochondria/chloroplast--otherwise they remain in cytosol