Cell structure Flashcards

1
Q

What classes of phospholipids are on the cytosolic side of the membrane?

A

Amino phospholipids (ex. phosphatidyl-ethaloamine and phosphatidyl-serine)

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2
Q

What classes of phospholipids are on the extracellular side of the membrane?

A

Choline derived phospholipids (ex. phosphatidyl-choline and sphingo-myelin)

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3
Q

What kind of lipid is sphingolipid?

A

Glycolipid from the golgi.

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4
Q

This functions as protection in the gut?

A

Glycocalyx - many covalently attached sugar groups

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5
Q

Where are the following synthesized?
Phosphoglycerides
Sphingomyelin
Glycolipids

A
  • ER
  • Golgi from sphingosine
  • Golgi from sphingosine
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6
Q

What is integrin?

A

It is a transmembrane protein that binds extracellularly to collagen or fibronectin as well as intracellularly to cytoskeleton (keratin)

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7
Q

Two integral membrane proteins in RBC plasma membrane?

A

Glycophorin and Band 3. Bind to cytoskeleton of actin and spectrin giving elastic properties.

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8
Q

Name protein for cell to cell adhesion?

A

cadherins

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9
Q

What determines if protein is translated into the ER membrane? What determines if it crosses the membrane?

A

Signal sequence of mRNA that recognizes SRP receptor in membrane. Protein translocator facilitates entry into membrane. The number and orientation of hydrophobic start/stop signals determines position in membrane.

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10
Q

What is the cellular pathology of cystic fibrosis?

A

It is caused by a faulty membrane protein (CFTR) that acts a chloride transporter. This transporter functions in formation of sweat, mucous, pancreatic digestive fluid, and other exocrine secretions.

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11
Q

Pathology of Duchenne muscular dystrophy?

A

It is caused by a mutation in dystrophin which is a protein linking an integral membrane complex with the actin cytoskeleton. There are 9 forms of muscular dystrophy but all are associated with loss of structural integrity at intracellular (actin) to extracellular (collagen) linkage.

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12
Q

What is the pathology of hereditary spherocytosis and what cells does it effect?

A

Dysfunction of mechanical support proteins in the RBCs. Ankyrin is covalently bonded to Band 3 integral membrane complex. Spectrin interlinks short actin protofilaments in the cytoskeleton normally.

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13
Q

Where is N-linked glycosylation and how?

A

Occurs in ER, modified in golgi. Linked to asparagine. N-linked makes up most of glycoproteins.

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14
Q

Where are O-linked glycoproteins made and what type does it produce.

A

Made in the golgi. Make proteoglycans.

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15
Q

Where are misfoled ER proteins degraded?

A

Degraded in cytosol. Detected in ER.

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16
Q

What do heat shock proteins do in the ER?

A

They are sensors for misfolding and respond by increasing transcription for chaperones, translocators, and proteasomes as well as decrease general protein synthesis.

17
Q

Where is lipid synthesis in cell?

A

Primarily smooth ER (high in hepatocytes)

18
Q

A cell that uses a lot of calcium likely has a lot of what organelle?

A

Endoplasmic reticulum.

19
Q

What organelle is reponsible for detoxification carried out by p450 enzyme?

A

Smooth endoplasmic reticulum.

20
Q

What is protein in cytosolic leaflet causing invaginations that give rise to uncoated vesicles?

A

Caveolae - usually goes to the golgi

21
Q

What are the two proteins in coated vesicles?

A

Clathrin - Lattice protein associated with trans side of golgi (Lysosomes)
Coatamer (Cop I and II) - Associated with cis side of golgi Cop I - From golgi to ER or plasma membrane
Cop II - From ER to plasma membrane

22
Q

Vesicle with KDEL amino acid sequence is going where?

A

It will associate with Cop I coat protein and go to ER

23
Q

Vesicle with M6P signal is going where?

A

To endosome/lysosome via clathrin coat

24
Q

What is the function of Rabs and SNAREs?

A

Docking of vesicle to target membrane

  • Rabs bind to inositol phospholipids on membrane
  • V-SNARES bind to T-SNARES