Endoplasmic reticulum Flashcards

1
Q

Important for intracellular —-storage

A

Ca+

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2
Q

RER makes most__ destined for secretion

A

protein

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3
Q

___embedded in the ER gives the rough appearance

A

ribosomes

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4
Q

Rough Er is the site of protein—- and —— also lipid —-

A

production and modification
lipid synthesis

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5
Q

Smooth ER is involved in lipid——, production of ——-and detoxification of —-

A

metabolism production of lipoprotein particles and detoxification of lipid soluble drugs

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6
Q

Transition ER are areas of—

A

smooth ER which form transport vesicles fro delivery to the Golgi

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7
Q

Smooth ER is important for intracellular —storage

A

Ca2+

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8
Q

Smooth microsomes have —-density and stop sedimenting and float at low sucrose concentration

A

low

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9
Q

Rough microsomes have a —-density and stop sedimenting and float at high sucrose concentration

A

high

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10
Q

ER reseals upon homogenization to form ——

A

microsomes

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11
Q

Proteins are either imported ——-or——-

A

co-translationally or post-translationally

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12
Q

Proteins are built from —- to —- term

A

N to C

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13
Q

The endomembrane system is composed of

A

the ER, Golgi, endosomes and lysosomes

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14
Q

RER appears in the ——micrographs b/c?

A

EM b/c of the ribosomes

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15
Q

RER is important for

A

protein folding and processing

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16
Q

What are the three ways proteins get translated?

A

translated completed
unfolded and then transported inot the ER lumen
co-translationally translocated

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17
Q

The smooth ER is important for?

A

storing calcium and detoxifying drugs

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18
Q

Both RER and SER are important for?

A

lipid biosynthesis

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19
Q

Proteins can enter the ER by which two ways?

A

post-translationally or co-translationally translocated

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20
Q

Co-translational translocation is dependent on?

A

an N-terminal signal sequence
the signal recognition patricle(SRP)
the SRP receptor and the translocon

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21
Q

What do stop transfer sequences allow for?

A

transmembrane domains to insert in cell membranes

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22
Q

What do start transfer sequences allow?

A

Non-N-terminal portions of the protein to iniate translocation

23
Q

Combination of start and stop sequences allow?

A

production of multi pass transmembrane proteins as well as transmembrane proteins with C rather then N terminus to the ER lumenal side

24
Q

What is N-linked glycosylation?

A

During translocation a block of 14 carbohydrates may be covalenty attached to the nitrogen on a asparagin residue within the recognition sequence Asn-X-Ser/Thr

Most proteins made at the RER are N-glycosylation in a co-translational manner by Oligosaccharyltransferase( a transmembrane protein complex of the RER)

25
The N-linked carbohydrates are only added in the —-and modified in the —-
ER Er and Golgi
26
p450 enzymes are associated with
SER membranes
27
p450 can?
oxidize drugs, this increases their solubility and may introduce OH groups which are sites for conjugation
28
What is conjugation?
is the process by which fairly large soluble molecules are covalently attached to OH groups which allows drugs to be removed by kidneys or intestines
29
What is the Golgi important for?
protein modification and sorting
30
The golgi is the site for?
O-linked glycosylation, which makes up about 10% of all protein glycosylation
31
What are the three components of the Golgi?
cis Golgi network medial cisternae tran Golgi network proteins have to move through this network in endosomes !> stationary cisternae model-vesiclules moving 2.cisternal maturation model-Sack matures into trans Anterograde movement is ER-Golgi-plasma membrane Retrograde Vesicleus-golgi-ER
32
The three compartments of the Golgi carry out ——functions thus requiring a —-of enzymes
distinctive specific set These enzymes must have either a system for retention or retrieval
33
____secretion occurs continuously
constitutive
34
—-secretion requires specific signal
regulated
35
Acid hydroplanes are modified by? This allows them to? What happens when the pH drops? What happens when this fails?
A mannose-6-phosphate(M6P) moiety in the golgi. This allows the, top binds to a M6P receptor which they are then packed into vesicles going to the lysosomes. As the pH drops, the cargo and receptor separate, with the receptor returning to the Golgi and the cargo going on to the lysosome. Failure leads to one or more hydrolases in the lysosomes, which mean cellular components are not broken down correctly. These diseases are collectively called as lysosomal storage diseases.
36
Secretion via vesicles is called?
ecocytosis
37
____can physically move vesicles around the cell. This requires any inputs of energy.
Motor proteins
38
What are the three types are motor proteins?
Kinesins dyneins myosins
39
____move towards the plus end of the mircotubules
kinesins
40
____move towards the minus end of the mircotubules
dyneins
41
___move along microfilaments
myosins
42
Endocytosis
taking components from outside the cell in vesicles
43
___is similar to endocytosis but it involves cytoskeletal rearrangements and it can be used to bring very large macromolecules even other cells into the cell
phagocytosis
44
Selection of endocytosis can be______ or ______
non-selective-pinocytosis selective-receptor-mediated
45
___form the vesicle, and they may be important for cargo selection by associating directly or indirectly with receptors
Coat proteins
46
The LDL-receptor associates indirectly with the____, allowing for selective uptake of LDL
coat protein clathrin
47
What are the three coat proteins?
Clathrin COPI COPII
48
Clathrin
out from the Golgi and in from plasma membrane triskelion-3 large and 3 small polypeptides polymerizes into a soccer ball shape Coat assembly initiated by ARFs(GTPase) Dynamin(GTPase) pinches off membrane
49
COPI
back from Golgi to ER initiated by ARF
50
COPII
out from ER utilizes Sar1 for initiation
51
Initiation of coat formation if mediated by
monomeric GTPases
52
Pinching off the vesicle requires a —
second monomeric GTPases called dynamin
53
Vesicular targeting requires a third monomeric GTPas called
Rab
54
SNARE complexes?
mediate membrane fusion of vesicles and target membranes. Generally there is a single helix on a vesicle and 3 on the target membrane. These spontaneously fold into a four helical bubble when they are close. The energy released from formation is used to drive membrane fusion, which is an unfavourable process