Secretory Pathway 2 (Golgi) Flashcards

1
Q

whats the name of the coat around vesicles going from ER to cis golgi?

A

COP2

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2
Q

whats the name of the coat around vesicles going from cis golgi to ER?

A

COP1

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3
Q

where are cop2 vesicles made?

A

SER

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4
Q

whats the pathway to a cop2 out of the ER?

A

RER>SER> COP2 vesicles via cytoplasmic tails of membrane proteins>out to cis golgi

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5
Q

What is ERGIC?

A

a receptor that helps certain clotting factors get packed into cop2/helps recruit coat. hemophilia if ERGIC mutation in liver

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6
Q

What if certain chaperones and other factors like Bip need to stay in ER? What are 2 ways?

A
  1. are part of larger complexes that don’t diffuse freely into COP2 zones, membrane proteins held by microtubules 2. if get packaged accidentally KDEL sequence gets bound by KDEL receptors in cis golgi and get repackaged back in cop1 to go back to ER
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7
Q

What happens at cis cisternae

A

mannose trimming and synthesis of M6P on lysosomal hydrolases

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8
Q

what happens at cis medial

A

sugars added : N-acetyl glucosamine

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9
Q

what happens at trans

A

Sialic acid (NANA) and galactose, negatively charged

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10
Q

What happens at trans golgi network right before protein gets transported out?

A

furin-mediated cleavage at certain dibasic amino acids, activates certain proteins like

HIV glycoprotein precursor, insulin receptor

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11
Q

Where can oligosaccharide-linked sugars be attached to?

What residues do they get attached to?

where does this happen???

A

glycoproteins and glycolipids…

attached to serine or threonine

The golgi

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12
Q

What are the 3 pathways that proteins can go after the golgi?

A

endosome/lysosome

plasma membrane (constitutive secretory pathway)

secretory granules

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13
Q

Explain secretory granule pathway (include explanation of proinsulin cleavage)

A

stimulation of secretory system..

acidic environemnt drives aggregation of proteins. proinsulin cleaved to insulin bc of acidic, insulin aggregates>maturation of granule

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14
Q

Explain the Endosomal/Lysosomal pathway from

ER>cis golgi>trans golgi>TGN>CCV>early endosome

A
  1. ER: N-glycosolation of asp residues via lysosomal hydrolase
  2. Cis golgi: GlcNAC phosphotransferase puts 1-phosphate on mannose
  3. Trans golgi: remove sugar and uncover m6p signal
  4. TGN: m6p binds to m6pR> CCV>fuse w early endosome lower pH causes receptor to be released
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15
Q

Elaborate on the constitutive secretory pathway…how can it happen and describe the separate domains of 2 types of polarized cells where it occurs

A

either directly trans golgi>plasma membrane or indirectly from endosome>plasma

neurons and epithelial cells

epithelial have apical an basolateral membranes

neurons have dendrite and axon membranes

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16
Q

Which proteins control vesicle docking? what type of an -ase are they

A

Rab. GTP-ase. Rab GTP as is part of vesicle and when docks to Rab effector proteins on membranes hydrolyzes.

17
Q

Which rab protein is involved in insulin docking and griscelli syndrome?

A

Rab 27. secretory pathway issues.

18
Q

What are the complexes that govern vesicle fusion? what are the two types by letter/protein? how many helices?

A

SNARE complex. V-snare=vesicle snare, synaptobrevin

T-snare, target synaxin

4 helices

19
Q

What are the proteins that bind ca and help form the SNARE complex?

A

synaptotagmins

20
Q

What can’t break the V complex thats usually used to break down plasma membrane proteins?

A

SDS

21
Q

What toxin can cleave SNARE to prevent fusion of vesicles?

A

botox