Lecture 14: Intracellular trafficking Flashcards

1
Q

What is the order of protein exocytic sequence?

A

RER -> SER -> (COPII) Cis
Golgi -> Trans Golgi ->(Clathrin) Secretory vesicle -> Exocytosis

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2
Q

What is the acronym that helps us remember COP proteins

A

COP’s investigation went
II steps forward and I step
backwards.

-COP 1: towards ER
-COP II: cell membrane

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3
Q

______________and ___________ are protein coats

A

caveolin and clathrin*caveolin linked to transcytosis

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4
Q

Endoscopes and lysosomes are made from _______________

A

golgi

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5
Q

____________________: Common 1 in every 250 individuals
Low Density Lipoproteins (LDL):
* Part of the transport system for cholesterol, needed by cells for membrane.
* Acquired through receptor-mediated endocytosis.
* Presentation:
* Xanthomas (cholesterol deposits in skin or
tendons like Achilles or wrist).
* Xanthelasma (cholesterol deposits in eyelids).
* Corneal arcus (deposits cause a white or gray
ring around iris)

A

Familial Hypercholesterolemia

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6
Q

Hypercholestrolemia can be homozyous or heterozygous. Can you explain what this means in terms of this disease?

A

Heterozygous -> Heart attack before 50 (men) or 60 (women)
* Homozygous -> High probability of cardiac death before 20 yo.

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7
Q

What happens in hypercholesterolemia?

A
  • Mutations in the LDL receptor can lead to non-binding or failure to internalize the receptor.
  • Less LDL internalized -> More LDL in circulation -> High Cholesterol in plasma -> Endothelial deposits -> Macrophage ingestion -> Foamy cell formation -> Atherosclerosis
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8
Q

______________ is a process that moves large molecules and waste out of a cell and into the extracellular space. It’s a type of bulk transport, which is a process that moves large numbers of molecules in and out of a cell

A

Exocytosis

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9
Q

_________ is where different models for profession and transport occur

A

Golgi apparatus.

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10
Q

__________ is involved in retrograde flow of membrane and return of proteins

A

COPI

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11
Q

___________ glycosylated proteins tags them for end-some and lysosomal transport

A

phosphorylation of mannose in N linked glycosylated protein tags

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12
Q

________________
Part of Lysosomal Storage Diseases (LSD).
* Presents in infancy with hypotonia, developmental delay, limited
mobility, clubfeet, and thickened skin.
* Frequent bone and joint abnormalities and umbilical and inguinal hernia.
* Narrow airway and thoracic abnormalities can lead to respiratory
infections and insufficiency. Often fatal in first decade.

A

I cell disease

Mucolipidosis

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13
Q

In Mucolipidosis or I cell disease what happens

A

Failure to phosphorylate mannose residues in lysosomes so lysosomes re secreted instead of transported

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14
Q

What are two two sides of the plasma membrane?

A

-Basolateral membrane: (end-some sorting)
-Apical membrane:

*There are specific signals that determine which side proteins or molecules go to

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15
Q

Maturation from vacuole to __________ occurs int eh regulated secretory pathway

A

secretory granule

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16
Q

In terms of secretory granules what is the movement?

A

Kinesins transport to the + end
of microtubules.

  • Dyneins transport to the – end of
    microtubules.
17
Q

What is the granule and vesicle fusion mediated by

A
  • SNARE complex: Synaptobrevin, Syntaxin, SNAP-25.
  • Synaptotagmin mediates fusion (controlled by [Ca++].
18
Q

Fusion regulators ____________. They regulate vesicular traffic and SNARE assembly.

A

RAB proteins

19
Q

Alterations in Rabs proteins reduce _________________

A

adipose cell response to insulin ->
Predisposition to insulin resistance.