Lecture 14: Intracellular trafficking Flashcards
What is the order of protein exocytic sequence?
RER -> SER -> (COPII) Cis
Golgi -> Trans Golgi ->(Clathrin) Secretory vesicle -> Exocytosis
What is the acronym that helps us remember COP proteins
COP’s investigation went
II steps forward and I step
backwards.
-COP 1: towards ER
-COP II: cell membrane
______________and ___________ are protein coats
caveolin and clathrin*caveolin linked to transcytosis
Endoscopes and lysosomes are made from _______________
golgi
____________________: 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)
Familial Hypercholesterolemia
Hypercholestrolemia can be homozyous or heterozygous. Can you explain what this means in terms of this disease?
Heterozygous -> Heart attack before 50 (men) or 60 (women)
* Homozygous -> High probability of cardiac death before 20 yo.
What happens in hypercholesterolemia?
- 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
______________ 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
Exocytosis
_________ is where different models for profession and transport occur
Golgi apparatus.
__________ is involved in retrograde flow of membrane and return of proteins
COPI
___________ glycosylated proteins tags them for end-some and lysosomal transport
phosphorylation of mannose in N linked glycosylated protein tags
________________
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.
I cell disease
Mucolipidosis
In Mucolipidosis or I cell disease what happens
Failure to phosphorylate mannose residues in lysosomes so lysosomes re secreted instead of transported
What are two two sides of the plasma membrane?
-Basolateral membrane: (end-some sorting)
-Apical membrane:
*There are specific signals that determine which side proteins or molecules go to
Maturation from vacuole to __________ occurs int eh regulated secretory pathway
secretory granule