DSA: Cell Organelles Flashcards

1
Q

4 functions of the ER

A
  1. Protein synthesis
  2. Lipid synthesis
  3. Protein folding
  4. Storage of calcium
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2
Q

Golgi apparatus functions

A

Post translational changes on proteins and lipids, trafficking

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3
Q

% of pancreatic exocrine cell membrane that is rough ER

A

60%

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4
Q

% of liver hepatocyte membrane that is mitochondria inner membrane

A

32%

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5
Q

3 topological categories of cell

A
  1. Nucleus and cytosol
    - communication through nuclear pore complex
  2. Organelles in secretory and endocrine pathway
    - ER, golgi, endosomes, lysosomes
  3. Mitochondria
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6
Q

What two compartments does the ER divide the cytoplasm in to

A

Luminal or cistern always compartment

Cytoplasmic or cytosolic compartment

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7
Q

3 important functions of rough ER

A
  1. Proteins modification and assembly
  2. Segregation of proteins for intracellular use
  3. Export proteins from the cell
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8
Q

How do most proteins exit the rough ER and where do they go

A

In vesicles transported to the cis portion of the Golgi apparatus

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9
Q

5 functions of smooth ER

A
  1. Glycogen metabolism
  2. Lipid and phospholipid synthesis
  3. Detoxification
  4. Steroidogenesis
  5. Calcium regulation
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10
Q

5 functions of the Golgi apparatus

A
  1. Modification of carbohydrates attached to glycoproteins and proteoglycans
  2. Polysaccharide and oligosaccharide synthesis
  3. Synthesis of sphingomyelin and glycosphingolipids
  4. Sorting secretory products
  5. Packaging and storing secretory products into secretory granules or vesicles
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11
Q

When does the golgi disassemble and reassemble

A

Disassembles during mitosis/meiosis

Reassembles in interphase

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12
Q

Clathrate coated vesicles

A

Vesicles are coated in clathrin; these vesicles are seen in the exocytosis/secretory and endocytosis pathway

Transport products from:
Golgi apparatus —> lysosomes

products from the exterior of the cell —> lysosomes

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13
Q

COP-coated vesicles

Coat protein

A

Transport products:

Between stacks of the Golgi apparatus (COP 1)

ER —> Golgi apparatus (COP 2)

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14
Q

2 important steps in the lysosomal sorting pathway

A
  1. Phosphorylation of lysosomal enzymes

2. Binding of lysosomal enzymes to M6P receptor

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15
Q

Primary lysosome

A

Storage site of lysosomal hydrolases

  • no digestive enzymes
  • homogenous
  • inactive enzymes
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16
Q

Secondary lysosomes

A

Engaged in a catalytic process

  • digestive enzymes
  • heterogenous
  • active enzymes
17
Q

Important step in endosome maturation

A

Lower internal pH to 5.5

18
Q

Familial hypercholesterolemia

A

Mechanism of cholesterol uptake is disrupted; characterized by elevated LDL (predominant cholesterol transport protein in the plasma)

High levels of LDL lead to atherosclerotic plaques

19
Q

4 functions of peroxisomes (micro bodies)

A
  1. Synthesis and degradation of H202
  2. Beta oxidation of long chain FA
  3. Bile acid and cholesterol synthesis
  4. Detoxify alcohol
20
Q

Zellweger spectrum disorders

A

Peroxisome biogenesis disorders caused by defect in assembly of the peroxisome; normally causes death within first year of life

21
Q

What type of cells typically would have lots of rough ER

A

Cell that make secreted proteins

22
Q

Lysosomes contain enzymes that are most active when

  • what do they do
A

At acidic pH

Break down proteins, carbs, lipids, nucleus acids