Zaidi Vesicular Traffic 2 Flashcards

1
Q

Lysosome contains about 40 different ____ enzymes.

For optimal activation, lysosomes require ___ ___ and an ___ environment.

This protein, ___ ___, pumps H+ into the lysosome to maintain the acidic pH inside.

The approximate acidity of a lysosome inside is near a pH of ___.

A

hydrolytic.

proteolytic cleavage. acidic.

Vacuolar ATPase.

5.

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2
Q

Lysosomes go through these three stages before becoming a lysosome

A

early endosome –> late endosome –> endolysosome –> lysosome.

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3
Q

These three pathways deliver materials to lysosomes:

A
  1. Phagocytosis
  2. Endocytosis
  3. Autophagy
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4
Q

During autophagy, the cytosol and organelles get engulfed into this structure, a(n) ___, which fuses with the ___ to make a ___.

A

autophagosome.

lysosome.

autophagolysosome.

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5
Q

Transport from TGN (trans golgi network) to lysosomes delivers ___ ___ and ___ to lysosomes.

The transported proteins to the TGN initially come from the ___, transported via the ___ ___.

TGN buds off into ___ and develops into ___.

A

membrane proteins. hydrolases.

Rough ER. Golgi complex.

endosomes. lysosomes.

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6
Q

This sorting signal ___ is located on the ___ ___, and they become attached to them in the ___.

M6P is recognized by ___ ___, which are located in the ___ ___ ___.

M6P receptors are packaged into ___-___ ___ that bud from the TGN.

Contents delivered into ___ and then to ___.

A

mannose-6-phosphate (M6P). lysosomal hydrolases. cis golgi network (CGN).

M6P receptors. trans golgi network (TGN).

clathrin-coated vesicles.

endosomes. lysosomes.

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7
Q

This enzyme, ___ ___, adds M6P to the lysosomal hydrolases. Without it the enzymes are not phosphorylated and not sorted into vesicles or delivered into lysosomes.

A

GlcNAc phosphotransferase.

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8
Q

Name two genetic defects in lysosomal hydrolases and describe them.

Both lead to accumulation of ___ ___ in lysosomes.

A

Hurler’s Disease (mutation in the enzyme required to break down glycosaminoglycan chains) and Inclusion Cell Disease (defective/missing GlcNAc phosphotransferase).

undigested material.

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9
Q

What is endocytosis? The plasma membrane does this to form the endocytic vesicle.

Large particle ingestion is referred to as ___. Small particle ingestion is referred to as ___.

A

Uptake of macromolecules from exterior.

PM invaginates and then pinches off to form the endocytic vesicle.

phagocytosis (ingested by phagosomes). pinocytosis.

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10
Q

T/F: The fusion of vesicles coming from the TGN is called endocytosis?

A

False. endocytosis only refers to uptake from the exterior of the cell’s plasma membrane.

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11
Q

What is a common example of receptor-mediated endocytosis?

Describe receptor-mediated endocytosis.

Receptor-mediated endocytosis provides a selective ___ mechanism.

Blockage of this pathway results in ___.

A

cholesterol uptake.

Used to import select macromolecules from the outside. Molecules bind to receptors on membrane surface, accumulating in clathrin-coated pits.

concentration.

Atherosclerosis.

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12
Q

Steps of cholesterol uptake:

A
  1. Endocytosis
  2. Uncoating (of clathrin)
  3. Fusion with Endosome
  4. Budding off of transport vesicles.
  5. Return of LDL receptors to plasma membrane.
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13
Q

The return of LDL receptors to the plasma membrane happens when vesicles bud off of this stage of endosome.

A

Early.

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14
Q

A defective ___ ___ ___, normally located in the clathrin coated pits, prevents ___ uptake by the cell. This leads to high levels of ___ in the blood, increasing the chance of forming atherosclerotic plaques.

A

LDL receptor protein.

LDL.

cholesterol.

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15
Q

This kind of tag helps to sequester endocytosed proteins.

What are three possible fates of endocytosed receptor proteins?

A

ubiquitin.

  1. degradation in endolysosome.
  2. transcytosis of transport vesicle.
  3. recycling of transport vesicles.
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16
Q

Binding of ___ acts like an intracellular signal, causing relocalization of glucose receptors from ___ ___ to the plasma membrane in order to increase glucose uptake.

A

recycling endosomes. insulin.

17
Q

These two WBCs are phagocytes.

Phagosomes fuse with ___ and ingested material is degraded.

___ material is secreted out by exocytosis.

A

macrophages and neutrophils.

lysosomes.

Undigested.

18
Q

phagocytosis is triggered by binding of particle to receptors on phagocyte surface. Binding triggers formation of ___ which engulfs the particle and forms ___.

Formation of pseudopod driven by localized ___ ___ and ___, and controlled by ___ ___ and ___ ___.

A

pseudopod.

phagosome.

actin polymerization. reorganization.

Rho GTPases. phosphoinositide signaling.

19
Q

This enzyme, ___, converts PIP2 to ___. This conversion causes the bacteria to get phagocytosed by WBCs.

A

PI 3-kinase.

PIP3.

20
Q

This process, where the cell ingests bits of PM, occurs continuously in all eukaryotic cells. The process begins at ___-___ ___. Invagination includes both the extracellular fluid and various solutes.

A

Pinocytosis.

clathrin-coated pits.

21
Q

Flash-shaped invaginations in the PM are known as ___, which are enriched in ___ and ___, and GPI-anchored.

The major structural protein of caveolae is ___. Caveolae invaginate into membrane by virtue of ___ ___.

A

Caveolae. cholesterol. glycosphingolipids.

caveolin.

lipid composition.

22
Q

T/F: Pinched off caveolae connect with lysosomes.

A

False. Caveolae do NOT connect with lysosomes.

23
Q

Exocytosis involves transport of vesicles from and to what cellular compartments?

Secretory pathways triggered by signals are called ___, and pathways operating continuously are called ___.

A

Exocytosis: From TGN to PM. Fusion of vesicles with PM is called exocytosis.

Regulated. Constitutive.

24
Q

Proteins destined for secretion are packed into secretory vesicles in the ___. The protein packing occurs via ___ ___.

TGN also promotes ___ ___ of the secretory proteins.

Proteins going back to the TGN are concentrated in clathrin-coated ___ vesicles.

A

TGN.

selective aggregation/clumping.

proteolytic processing.

retrieval.

25
Q

Name the two types of t-snares.

v-snares, aka ___, is located on the lumen of the synaptic vesicle.

Name the 5 steps of synaptic vesicle exocytosis.

A

SNAP25 and syntaxin are the two types of t-snares.

synaptobrevin.

  1. Docking
  2. Priming I
  3. Priming II
  4. Fusion Pore Opening
  5. Fusion Complete
26
Q

Calcium binds to this protein on the synaptic vesicle, ___. This functions to remove the ___ block of the SNARE bundle.

This allows the fused pore to do what?

A

synaptotagmin.

complexin.

Removing the complexin block allows fusion pore binding and opening.