Endoplasmic Recticulum (ER) Flashcards

(45 cards)

1
Q

ER

A
  • startinf point for scretoru and biosythestic pathway
  • lumen is aquaous space inside tubules and citrune
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2
Q

reticulons

A

mediate tubules and cistrnae shape

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3
Q

rough ER

A
  • mostly cisternae with bound ribosomes
  • protein and membrane phospholobid sythesis
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4
Q

smooth ER

A
  • mostlycurved tubules lacking ribosome
  • Ca2+ storage
  • hormone sythesis
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5
Q

nuclear envelope

A

outer nuclear membrne continous woith RER

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6
Q

mitochondria and plasma membrane-associated membranes

A

ER regions make direct contact with mitochondria or pm

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7
Q

ER exit sites

A

transport vesicles bud off enroute to golgi

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8
Q

free ribosmes in cytoplasm

A

remains in cytoplasm or targets to proper intracellular compartment

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9
Q

membrane bound ribosomes

A
  • remains localized in ER subdomain
  • localixes to other ER derived organelles
  • goes from ER to ? endomembrane compartment
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10
Q

cotranslation of soluble protein into RER lumen

A
  • in cytoplasm tranlation of ribisome begins
  • N terminus emerges containing signal sequence
  • recognized by signal recognition protein which bind and stips translation
  • SRP binds to receptor (RER surface)
  • GTP hydrolysis release SRP
  • polypeptide and ribsome transferred to cytoplasmic side of sec 61 translocon
  • n terminus inserted into opening of tanslocon channel
  • signal peptidase cleaves N terminus into lumen
  • protein enters lumen and pre closes
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11
Q

sec 61 translocon

A

contains pore ring

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12
Q

membrane protein topology

A

of membrane spanning domains and orientation

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13
Q

tran membrane doemain

A
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14
Q

single pas integral membrane protein

A

Type l (STA)
Type ll (SA)
Type ll (SA)

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15
Q

Multi-spanning integral membrane protein

A

type lV (STA and SA)

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16
Q

stop transfer anchor vs signal anchor

A

stop (STA)
signal (SA)

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17
Q

positive outside rule

A
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18
Q

membrane bilayer asymetry

A
  • membrane proteins and lipids distribited in nilayer aymetry
  • exoplamic
  • cytoplasmic
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19
Q

glycosylations

A

most proteins sythesized in ER are glycoproteins linked to one or more sugar chains

20
Q

N linked glycosylation

A

(addition of sepcific chains foo sugaR monomer)
1) core glycosyltrone: glycoytranferase senthisizes core oligosaccharides
2) core modification
3) tranfer core oligosachride from diolchol lipid carrier to nacsent soluble protein (specific aa seq, -N-X-Sh-)
4) 2/3 terminal glucose unites removed by glucocidses

21
Q

protein disulfied isomerse (PDI)

A

catalyizes formation of intra/intermolecular disulfide bonds

22
Q

ER protein quality control

A

rectoplasmins and PDI help mediate proper foldinf and stability
oligomeric assembly

23
Q

if a protein is properlu folded one manlose unit removed by er mamolidase and

A

becomes er resident
goes to golgi

24
Q

UGGT monitoring enzyme

A
  • recongnizes if protein is released from retocplasmins is misfolded
  • adds back single glucose to oligosachride core
  • binds back to calexon
25
ER protein degredation
- AAA ATPase p97 (ATP hydrolisis pull misfolded proteins across membrane into cytosol) - into cytoplasm oligosacride removed and misfolded by poly ubiquitin
26
mono UB
- signal for targetinf membrane proteins
27
poly UB
signal for degradation and degrade by protesomes
28
protesome
- barrel shapped multi subunit degradifinf machine in cytoplasm - bind cap or lib - poly UB removed (recycled) - protein threaded into prelesome degradation prokeolisis
29
unfolded protein response pathway (UPR)
to much misfolded proteins in er er stress Ire1 Perk Atrg all regulate different pathway (Perk and Atrg stress sensing domain inactive by Bio)
30
Perk mediated UPR pathway
- Bip release - perk dimerizes (active) - phosporylate eIF2a (stops protein synthesis) - chaperones (bip available to focus on misfolded proteins)
31
ATF6 mediated UPR pathway
- Bip Release - active AFF goes ER -> Golgi - trancription factor domain cleaved by golgu acociated protease - strand factor target nulcease upregulates genes encoding key proteins in quaternary control
32
ER exit sites (ERes)
- subdomain of ER located next to cis face of gGolfi complex - responsible for budding to send to golgi
33
COat proteins (COPs)
- assemle on cytpoplasmic surface of ERes 1) mediate membrane curvature and formation of vesicles 2) recognize and concentrate specific cargo components into vesicle
34
COPll
move ER to Golgi
35
COPl
move backward Golgi to ER
36
clathrin
- golgi->Golgi-> ER - plasma membrane -> endosomes
37
retrograde transport
38
COPll assembly
Sar1 reqruited - binds to sec12 (guanosine exchange factor GDP->GTP) - SAR 1 binding to GTP binding causes conformational change (exposes N terminus Sar 1 GTP integrated into cytoplasmic facing leaflet of ERes membrane bulayer Sar 1 GTO binds to other copll - recruits sec23 and sec 24 (promote bending)
39
Anterograde vs retrograde vesicle transport
40
vesicle docking and fusion at CGN
- mediated by Rab proteins - rabs and rab effector binding conveys vesicke targetinf specifity and docking
41
snare proteins
- after dockinf they initiate fusion v snare: on transport vesicle T snare: on target AA receptor both interact with snare complex
42
snare motif
cytoplasmic facing coiled coil domain in V and Extend from vesicle target
43
membrane fusion occurs when...
NSF and SNAP mediate disasembly of snare complex
44
ER rtreval sorting signalinf
c terminal - kdel sequence and ce terminal siysre sequence
45
kdel receptor
recognixe escaped soluble ER proteins