mod 4 Flashcards

1
Q

what are the components of the endomembrane system?

A

ER, golgi , endosomes and lysosomes (NOT perosixomes)

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2
Q

Cotranslational import

A

peptide moves across the ER to remain or is transported by vesicles to endomembrane system (ribosome on ER)

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3
Q

posttranslational import

A

peptides for cytosol or nucleus, mito, chloroplasts, or peroxisomes move via postranslational (free ribosomes)

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4
Q

first 3 steps of the signal mechanism

A
  1. signal recognition particle binds to er’s signal sequence and ribosomal subunit stopping translation
  2. SRP and SRP receptor binds and the ribosome and the translocon
  3. the SRP’s bind a GTP each so pore opens and polypeptide is inserted
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5
Q

4-6 steps of signal mechanism

A
  1. GTP hydroylsis releases the SRP
  2. signal sequence is cleaved by signal peptidase
  3. polypeptide is released in the ER lumen, ribosome is releaseed and translocon pore closes
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6
Q

occurs with internal stop transfer sequence and a terminal ER sequence

A

the stop of the protein halts the translocation and moves to the side in the translocon to anchor the polypeptide so the N-terminus is in the ER lumen and the C-terminus in the cytosol.

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7
Q

occurs w single internal start transfer sequence

A

the polypeptide loops straight thru the channel starting at the sequence

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8
Q

N-glycosylation

A

proteins made at RER cotranslationally by oligosaccharyltransferase (protein complex), they are added to an ASN. Has a nitrogen in the link.

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9
Q

where is drug detoxification?

A

the smooth ER in liver cells, hydroxylation is the first step, the p450 in the liver plays huge role

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10
Q

functions of the smooth ER

A

lipid metabolism, detoxification, caro metabolism, calcium storage, steroid biosynthesis.

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11
Q

where are most phospholipids and cholesterol are made ?

A

on the cytosolic face of ER

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12
Q

specifications of lipid biosynthesis

A

flippases (double membrane), even distribution and asymmetry.

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13
Q

Golgi faces, and 2 models of formation

A

cis- oriented towards ER and trans- face away.
1. stationary cisternae model and cisternal maturation model
membrane incresaes in thickness from 5 to 8nm

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14
Q

Anterograde and retrograde transport

A

anter- ER - golgi - plasma mem.
retro- vesicles from golgi- ER

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15
Q

N-linked glycosylation

A

starts in ER, folds the proteins, and modifies the N-glycosyl group, attaches to serine or threonine.

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16
Q

what could keep proteins retained?

A

kin recognition (cluster to avoid going in vesicles), retention tags keep them in ER ( receptors bind to tags), and retrievel tags, KDEL and KKXX

17
Q

Constitutive secreation and regulated

A

always on, default pathway, unregulated
regulated- vesicles fuse w mem. w a specific signal, and bud from TGN

18
Q

what is receptor mediated encodytosis

A

also clathrin dependent endocytosis, need receptors on outer membrane. can hold about 1000 receptors, more than 2 different receptors have been identified

19
Q

low density receptor mediated endocytosis

A

holds cholesterol

20
Q

caveosomes

A

lipid rafts

21
Q

all the coat proteins

A

Clathrin: PS to endosomes
COPI: golgi to ER
COPII: PS to ER

22
Q

clathrin coat

A

initiated by ARF (GTpase) , dynamin pinches off the coat

23
Q

dynamin

A

binding domain and GTPase domain

24
Q

COPI and COPII coat

A

COPI: initiated by ARF protein
COPII: initiation of Sar1

25
Q

Snare

A

stable and favourable fusion by the interact of v-snare w t-snare, Snap and NSF take it off