Cell Membrane Trafficking Flashcards

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1
Q

Why is membrane trafficking needed?

A
  • Cell compartmentalisations
  • Movement of signals
  • Modifications
  • Retrieval of proteins
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2
Q

What are the two types of membrane trafficking?

A
  • Endocytic
  • Exocytic
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3
Q

How are proteins modified?

A

Addition of oligosaccharide in the ER
Processing in the golgi

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4
Q

What does N and O linked glycosylation do?

A

Assists folding
Acts as a ligand

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5
Q

What are the advantages of using yeast as a model organism?

A
  • Whole genome is sequenced
  • Amenable for study (can be diploid or haploid)
  • Limited gene diversity
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6
Q

What are the disadvantages of using yeast as a model organism?

A
  • Limited diversity
  • Small
  • Not mulitcellular
  • Has a cell wall
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7
Q

What is endocytosis?

A

The invagination of the plasma membrane into the cell producing a vesicle that fuses with endosomes

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8
Q

What was Novick and Shekman 1980’s hypothesis for the yeast experiment to identify membrane trafficking genes?

A

If proteins were not secreted, the cell would become more dense because of the build up of vesicles.

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9
Q

What are secretory (sec) mutants?

A

Cells that synthesis the protein but fail to export and secrete it.

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10
Q

How many genes were identified in the 1980 yeast experiment?

A

23.

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11
Q

Why were not all genes identified in the 1980s yeast experiement?

A

The test only tested for genes under the effect of temperature.
Only considered transport to the membrane.

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12
Q

How many genes in the 1980 yeast experiment were involved in endocytosis?

A

5

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13
Q

How is alpha factor and CPY easy to follow?

A

They are glycosylated and proteolytically cleaved.

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14
Q

What are the possible destinations from the late golgi?

A
  • Membrane
  • Early endosome
  • Later endosome
  • Vacuole
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15
Q

What is a MVB

A

Multi Vesicular body

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16
Q

What happens to CPY after the late golgi?

A

Recognised by receptor Vps10
CPY dissociates and travels to MVB/Late endosome
Vsp10 is retrieved back to late golgi.