Cell Trafficking Flashcards

1
Q

_ is the distribution center for proteins and lipids from the ER to vexicles and plasma membrane

A

golgi

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2
Q

what are the posttranslation events in the golgi

A

addition of N-oligosachrides to asparginine

addition of O-oligosacchrides on serine and threonine

addition of mannose 6-phospahte to proteins

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3
Q

_ are the sorting centers for material outside of the cell or from the golgi sending it to lysosomes for destruction or back to the golgi for further use

A

endosomes

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4
Q

what is I cell disease

mutation?

failure in?

A

inclusion cell disease aka mucolipidosis type II

that is an inherited lysosomal storgae disease (AR)

mutation in N-acetylglucosaminyl-1-phosphotransferase

failure in phosphorylating mannose residues on glucoproteins in the golfi so enzymes are secreted extracellularly instead of eliminated via lysosomes

the lysosomes are decifent in digestive enzymes and inculsion bodies form inside of the lysosomes

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5
Q

symptoms of Inclusion cell disease

A

coarse facial features, gingival hyperplasia, corneal clouding, restricted joint movement, increased plasma levels of lysosomal enzymes

fatal in childhood

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6
Q

what is a signal recognition particle

A

a protein that is in the cytosol that tranfers ribosomes to the RER

*def= accumulation of proteins in the cytosol

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7
Q

COP I vesicular traficking

A

golgi to golgi (retrograde)

cis golgi to RER

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8
Q

COP II vesicular trafficking

A

ER to cis GOGI (retrograde)

Two steps foward (anterograde) one step back (retrograde)

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9
Q

clathrin trafficking

A

trans-golgi to lysosomes, plasma membrane, and endosomes

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10
Q

what are the three types of signaling

A

autocrine (self)
paracrine (neighboring)
endocrine (through the blood stream)

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11
Q

what are the steps of a cell signaling pathway

A

reception (receptor binds to a ligand)
transudction (change in reception, 2nd messenger)
Cell response

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12
Q

what are the cell receptors (most common)

A

G protein, enzyme couples, ion channel receptors

g protein- 7 transmembrane that avtivates G proteins

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13
Q

what happens when a ligand binds a g protein coupled receptor

A

GDP is exchanged for GTP on the alpha subuit which activates the protein and seperates from the beta and gamma subunits and it is not free to interact with other proteins

GDP is the resting state

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14
Q

what are the three types of G proteins ?

A

Gq, Gi, Gs

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15
Q

Gq protein activates what

A

phospholipase Cā€”> DAG and IP3

IP3 goes into the ER and releases calcium into the cytoplasm and depolarization

DAG binds to PKC (relies on Ca+ to activate)

PKC adds phosphate groups to proteins and activates them

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16
Q

protein Gs activates what

A

adneylate cyclase - takes ATP and removes 2 phosphate groups to create CAMP

CAMP binds PKA at the regulatory subunit

regulaltory and catalytic subuit of PKA dissociate and the catalytic subuit will phosphorylate proteins

17
Q

Gi inhibition

A

negative feedback on G3

inhibits adenylate cyclase

18
Q

what is an enzyme coupled receptor

A

single pass transmembrane protein with intrinsic enzyme activity

receptor domain and eznyme domain (protein kinase that phosphoylates the receptor domain)

19
Q

what are the 3 main types of enzyme couple receptors

A
  1. Receptor tyrosine kinase: dimerize and cross phophorylate
  2. tyrosine kinase associated receptor- cytoplasmic tyrosine kinase (no intrinsic ability
  3. receptor serine/threonine kinase: Type 1 and Type 2 ,type 2 activates type 1, type 1 will phosphorylate other proteins.
20
Q

what are ion channel receptors

A

usually closed, but bind to ligands and open up; allow ions to flow down their gradient and trigger a cellular response

21
Q

water channel

A

aquaporins

22
Q

bulk transport

A

endocytosis and exocytosis

need ATP to work

23
Q

endocytosis types

A

phagocytosis- WBC; phagolysosome
pinocytosis- vesicle (takes in solutes), kinesin and dyenin
receptor mediated endocytosis- LDL (clathrin coated pits)- endosome

endsome sepreates the receptor and the ligand (receptor recycling)

24
Q

exocytosis starts where

A

in the golgi apparatus

takes proteins, lipids and hormones to vesicles