Endomembrane System Flashcards

(55 cards)

1
Q

Rough ER Jobs

A

1- adding carbs to glycoprotein
2- folding of polypeptides
3- fixing misfolded proteins
4- assembly of multimeric proteins

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2
Q

Smooth ER Jobs

A

1- drug detoxification
2- carb metabolism
3- calcium storage
4- steroid biosynthesis

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3
Q

Hydroxylation

A

NADPH dependent process of adding OH groups to drugs to make them easier to excrete

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4
Q

cytochrome p-450

A

protien catalyst of hydroxylation

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5
Q

glucose-6-phosphatase

A

converts glucose-6-phosphate to free glucose in carb metabolism

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6
Q

HMG-CoA reductase

A

commited step in cholesterol biosynthesis

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7
Q

flippases

A

transfer phospholipids from the cytoplasm to the ER lumen

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8
Q

phospholipid exchange (transfer) proteins

A

move phospholipids to designated organelles (mitochondria, chloroplast, or peroxisomes)

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9
Q

Golgi Role

A

further processing, sorting, and packaging of membrane lipids

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10
Q

N-glycosylation/O-glycosylation

A

Addition of side chains to the N of asparagine or OH of serine, threonine, or tyrosine to create a glycoprotein

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11
Q

Core oligosaccharide

A

2x N-acetylglucosamine, 9x mannose, 3x glucose. Beginning side chain of all glycoproteins until trimmed and modified in the ER lumen

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12
Q

cotranslational glycosylation

A

addition of oligosaccharide as the polypeptide is being formed

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13
Q

calnexin/calreticulin/ERp57/UGGT

A

form a protein complex to promote proper folding and disulfide bond formation of glycoproteins

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14
Q

terminal glycosylation

A

further processing of glycoproteins withing the golgi, involving removal and addition of units to the core oligosaccharide

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15
Q

protein tag

A

targets the protein to a transport vesicle that will take it to the right location

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16
Q

posttranslational import

A

uptake of completed polypeptides with targeting signals into their designated organelle (after translation in cytoplasm)

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17
Q

cotranslational import

A

polypeptide is brought into the ER as synthesis occurs (stays in endomembrane system)

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18
Q

signal hypothesis

A

polypeptides destined for ER have an ER signal sequence that direct the mRNA to the RER

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19
Q

preprotein

A

protein containing an ER signal sequence

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20
Q

SRP (signal recognition particle)

A

mediates the contact of the ribosome to the ER

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21
Q

translocon

A

structure of ER membrane responsible for translocation of polypeptides across the ER membrane

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22
Q

retention tag

A

protien tag that keeps them in the ER

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23
Q

retrieval tag

A

tag on proteins that return from the golgi to the ER

24
Q

mannose-6-phosphate

A

tag that sends lysosomal proteins to lysosomes

25
Hsp70
chaperone that keeps the protein unfolded during posttranslational import
26
sec62/63/7172 and Sec6
protein complex that targets cytosolic proteins for translocation
27
BiP + ATP hydrolysis
pulls polypeptide into ER lumen
28
constitutive secretion
vesicles move directly to cell membrane and fuse with plasma membrane
29
regulated secretion
vesicles accumulate in the cell and fuse with membrane ONLY in response to specific signals
30
polarized secretion
exocytosis limited to specific surface of the cell
31
Clathrin depended endocytosis
ligands bind to receptors on the membrane surface to internalize macromolecules
32
fluid-phase endocytosis
pinocytosis for nonspecific internalization of extracellular fluid
33
coated vesicles
vesicles in protien/lipid transport covered in layers of protein (clathrin/COPI/COPII)
34
caveolin/clathrin/COPI/COPII
proteins associated with coating vesicles for transport
35
Clathrin/adaptor protien(AP)/dynamin
coats involved in clathrin-coated vesicles
36
triskelion
3-legged structure of clathrin proteins
37
AP complexes
sites of regulation of clathrin assembly/disassembly (ATP/GTP dependent)
38
dynamin
required for constricting and closing clathrin vesicles
39
COPI/COPII
involved in retrograde transport from golgi to ER and between golgi cisternae
40
SNARE/SNAP protein
Involved in proper sorting and targeting of vesicles. Allow recognition between vesicles and targets
41
v-SNARE
SNARE proteins found in vesicles
42
t-SNARE
SNARE proteins found on target membranes
43
acid hydrolases
Enzymes found in lysosomes. Activation is the last step in lysosomal development from endosome --> lysosome
44
Heterophagic lysosome
contain substances that originated outside the cell
45
autophagic lysosome
contain materials originating inside the cell
46
residual body
lysosomes once digestion ceases
47
autophagy
method of breaking down cellular structures that are damaged or unneeded
48
macrophagy
form of autophagy where an organelle is wrapped in a double membrane from the ER forming an autophagosome
49
microphagy
form of autophagy in which a small vacuole is surrounded by a single membrae bilayer
50
glycogeneosis/hurler/tay-sachs
lysosomal storage diseases leading to the accumulation of substances that cannot be broken down
51
plant vacuole
Act as lysosomes as well as maintaining turgor pressure, regulating pH, and storage
52
peroxisome
Vesicle stemming from the ER that contains catalase and cyrtalline. 1- Peroxide metabolism 2- Detoxification 3- Fatty acid oxidation 4- Metabolize N-containing compounds 5- Catabolism of unusual substances
53
plant peroxisomes
associated with aspects of cell energy metabolism and in close contact with mitochondria and chloroplasts
54
glycoxysomes
specialized plant peroxisome in seedlings
55
peroxins
proteins required for the process of increasing number of peroxisomes in a cell