Cell trafficking Flashcards

1
Q

Name the 3 cell signaling pathways steps

A

1 Target cell rec binds to ligand
2 transduction - activation of intracellular messenger
3 cell response

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2
Q

Name the 3 classes of receptor

A

GPCR
Enzyme coupled receptor
Ion Channel receptor

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3
Q

Which of the class of receptors is serpentine

A

GPCR

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4
Q

Explain the pathway of GPCR

A

g protein binds to gdp (inactive)—> binding of ligand—> GDP converts to GTP and bind to alpha subunit—–> alpha subunit brings in changes—-> these changes require gtp to convert to gdp——> gdp inactivates gpcr

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5
Q

Which pathway does Gq activate

A

Phospholipase C which forms IP3 and DAG

IP3 opens Ca and DAG uses them to activate kinase and cause changes

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6
Q

Which pathway does Gs activate

A

By adenylyl cyclase —-> activates cAMP—-> binds pKa—–> dissociates regulatory subunit

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7
Q

What are 3 types of Enzyme Coupled receptor

A

i) Receptor tyrosine kinase
ii) Tyrosine kinase associated receptor
iii) Serine threonine kinase

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8
Q

Give the mechanism of Receptor tyrosine kinase

A

ligand binds—> dimerization—-> partial activation——> cross phosphorylation—-> Ras activation——–> MAP kinase

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9
Q

Which toxin inhibits Gi

A

Cholera toxin and Pertussis toxin

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10
Q

what are the 3 types of endocytosis

A

Phagocytosis
Pinocytosis
Receptor mediated endocytosis

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11
Q

Steps involved in phagocytosis

A

binding of subs to rec—-> pseudopod formation—-> phagosome formation—> binding of phagosome with lysosome to form phagolysosome —-> digestion of subs

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12
Q

Both endocytosis and exocytosis require atp (T/F)

A

True

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13
Q

What mechanism does receptor mediated endocytosis follow

A

Clathrin mediated endocytosis

clathrin also transports trans golgi to lysosome

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14
Q

What organelle is the distribution center for proteins

A

Golgi

From ER to vessicles

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15
Q

What are the post translational modifications that take place in the Golgi apparatus

A

modifying N oligosaccharide on asparagine
Adding O oligosaccharide on serine and threonine
Adding mannose 6 phosphate to proteins from lysosome

3. N acetylglucosaminyl 1 phosphotransferase

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16
Q

What are the sorting center for material from outside cell and Golgi

A

Endosome

send to lysosome for destruction and golgi for further use

17
Q

I cell disease is also known as

A

Mucolipidoses type 2

18
Q

genetic makeup of I cell disease

A

Autosomal recessive

19
Q

Reason of I cell disease

A

Loss of enzyme N acetylglucosaminyl 1 phosphate which adds mannose 6 phosphate to proteins

20
Q

Mechanism of I cell disease

A

def in N acetylglucosaminyl 1 phosphate—–> failure of golgi to phosphorylate mannose—-> enzyme secreted extracellularly than in lysosome —–> lysosome def in dig enzymes—–> Buildup of cellular debris in lysosomes called inclusion bodies

21
Q

Symptoms of I cell disease

A

Coarse Facial features
**Gingival hyperplasia
**corneal clouding
claw hand
restricted joint movement
kyphoscoliosis

22
Q

What does dysfunctional SRP cause

SRP- signal recognizing particle

A

Accumulation of protein in cytosol

23
Q

COPI and COPII transport

A

COPI - retrograde (Golgi to Golgi or cis golgi to ER)
COPII - anterograde (ER to cis golgi)

Two steps forward one step back

24
Q

Signal ______ is the process where a receptor protein changes in response to binding a ligand and activates the second messenger proteins.

A

Transduction

25
Q

Gq protein activates the enzyme _____

A

Phospholipase C