Zaidi: Trafficking 2 Flashcards

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1
Q

Antibody interaction in phagocytosis

A

Antibodies bind to microbe, Fc chain recognized by Fc receptor on macrophage/neutrophil
Binding triggers formation of pseudopod which engulfs particle and forms phagosome

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2
Q

Regulated secretory pathway

A

Triggered by signals

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3
Q

Blockage of cholesterol uptake pathway results in

A

Atherosclerosis

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4
Q

Constitutive secretory pathway

A

Operates continuously

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5
Q

Hurlers disease

A

Mutation in the enzyme required to break down glycosaminoglycan chains

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6
Q

GlcNAc phosphotransferase

A

Transfers GlcNAc-Pi to mannose to create GlcNAc-M6P

GlcNAc is then removed and you have M6P

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7
Q

Phagocytes include

A

WBCs such as macrophages and neutrophils

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8
Q

Storage of receptor proteins in recycling endosomes

A

Receptor proteins such as glucose transporters can be stored in endosomes.
Cell recieves signal that it needs more glucose when insulin binds insulin receptor
More glucose transporters are then transported to membrane from endosomes

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9
Q

Proteins destined for secretion are packaged where and involves what

A

Into secretory vesicles in the TGN

Involves selective aggregation/clumping of proteins

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10
Q

Lysosomal storage disease

A

Genetic defects in lysosomal hydrolases

Accumulation of undigested material in lysosomes

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11
Q

Vesicle coat involved in pinocytosis

A

Clathrin coated pits

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12
Q

Proteins are concentrated into vesicle by

A

Retrieval of other proteins that go back to TGN and ER

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13
Q

Pseudopod formation driven by and controlled by

A

Driven by localized actin polymerization and reorganization

Controlled by Rho GTPases and PI signaling

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14
Q

LDL receptors have binding site for

A

Clathrin, to ensure the vesicle forms around the LDL receptors

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15
Q

Membrane protein/hydrolases transport to lysosomes

A

Co-translationally transported into RER and then transported via golgi complex to TGN
TGN buds off into endosomes which develop into lysosomes

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16
Q

Phagocytosis

A

Large particles ingested by phagosomes

17
Q

What happens to undigested material

A

It is secreted through exocytosis

18
Q

Lysosomal hydrolases have what sorting signal

A

Mannose-6-Phosphate is attached to them in the Cis golgi network
M6P receptors in TGN recognize the sugar

19
Q

Vacuolar ATPase

A

Pumps H+ into lysosomes to maintain acidid pH and drive transport of small metabolites

20
Q

Caveolae

A

Flask-shaped invaginations in PM, enriched in cholesterol and glycosphingolipids
Major structural protein is Caveolin

21
Q

TGN promotes

A

Proteolytic processing of the secretory proteins- activation mechanism

22
Q

Inclusion cell disease

A

All of the lysosomal hydrolases are missing in many cell types. Undigested substrates accumulate as “inclusions”

23
Q

Defective or missing GlcNAc phosphotransferase

A

Lysosomal hydrolases with mannose are never phosphorylated to create M6P.
Therefore, hydrolases do not get delivered to lysosomes, they are carried to cell surface and secreted

24
Q

Caveolae invaginate into membrane by virtue of, they pinch off from PM by

A

Lipid composition, NOT the clathrin coat
Pinch of PM by dynamin-form caveosome
These DO NOT connect with lysosomes

25
Q

Exocytosis route

A

Transport vesicles move from TGN to PM

26
Q

What happens to LDL receptors after they successfully bring LDL into endosomes

A

They are recycled back to the plasma membrane

27
Q

What type of vesicles bud off from TGN to create endosomes

A

Clathrin-coated vesicles

28
Q

Receptor-mediated endocytosis

A

Imports select macromolecules from outside cell
They bind receptors on membrane and accumulate in clathrin coated pits
Example of this mechanism is cholesterol uptake

29
Q

Endocytosis

A

Uptake of macromolecules from exterior across plasma membrane

30
Q

Pinocytosis

A

Small particles ingested by pinocytic vesicles

31
Q

Lysosomes are derived from and contain

A

Late endosomes

Contain hydrolytic enzymes