Cell Bio II Flashcards

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1
Q

Integral Proteins

A

Can go either all the way across the membrane, or just partway

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2
Q

Peripheral Proteins

A

Can be removed from the plasmalemma with salt solutions

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3
Q

Symptoms of Creutzfeldt-Jakob disease

A

ataxia, dementia, paralysis

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4
Q

Lab results in Creutzfeldt-Jakob disease

A

spongiform change in cerebrum and kuru plages of abnormal aggregates in cerebellum. Can use PAS or congo red to see

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5
Q

How does Creutzfeld-Jakob disease happen

A
  • Normal prion gets converted to abnormal form
  • Abnormal makes cross-linked filaments that are resistant to proteolysis
  • Stimulates production of more abnormals over wild type
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6
Q

Functions of membrane proteins

A

Pumps and carries, channels, receptors, linkers, enzymes, and structural proteins

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7
Q

Na+/K+ATPase Pump

A

cleaves ATP to transports Na+ out of the cell and K+ into the cell. Regulates intracellular volume

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8
Q

Digoxin

A

Partially inhibits the Na+/K+ pump, leading to decrease in the activity of Ca/Na transporter which increases sacroplasmic Ca ion concentration, which improved cardiac pump performance

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9
Q

Co-transport of glucose and Na

A
  • example of secondary active transport
  • Does not require ATP
  • Na+ and glucose are co-transported into the cell as Na moves down it’s conc. gradient
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10
Q

Multidrug resistant transports

A

subfamily of primary transport proteins that are ATPases

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11
Q

MDR-1

A

expressed in kidny, liver, intenstine and blood-brain barrier. Transports drugs

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12
Q

MDR-2

A

transports conjugated (direct) bilirubin

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13
Q

MDR-3

A

expressed in liver. Flippase of phosphatidylcholine

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14
Q

Dubin-John Syndrome

A
  • Caused by mutation in ATP binding region of MDR-2 Protein.

- Impaired transcription and mislocation of the MDR-2 protein

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15
Q

Cystic Fibrosis

A

-mutation in CFTR, which is a chloride channel that regulates Na+ and HCO-3. Causes salty sweat, viscous secretion in intestine, pancreas, bile duct, and airways.

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16
Q

Lab findings in DMD and becker muscular dystrophy

A

pale staining muscle fibers lacking dystrophin

17
Q

5 pathways of endocytosis

A
  1. Macropinocytosis
  2. Clarthrin-dependent (mediated) with and without receptors
  3. Nonclathrin/noncaveolar
  4. Caveolar-dependent
  5. Pagocytosis-actin dependent