Cell Orgnells Flashcards

1
Q

What is the plasma membrane and what are its functions?

A

Outer body of the cells, bilayer.

-Protective barrier, has transporters, signaling

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2
Q

What is the nucleus and what are its functions.

A

The nucleus contains the genome.

It is the principle site for DNA and RNA synthesis.

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3
Q

What is the cytoplasm and what is its function.

A

The cytoplasm consists of cytosol and cytoplasmic organelles.
-Intermediary metabolism

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4
Q

What is the Endoplasmic Reticulum (ER) and what are its functions?

A

-Ribosomes attached-(Rough ER)
-No Ribosomes - (Smooth ER)
It is involved in protein synthesis, lipid synthesis, protein folding, and storage of calcium.

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5
Q

What is the GOLGI APPARATUS and what are its functions.

A

The golgi apparatus is composed of stacks of disc-like compartments.
-It is involved in post-translational changes on proteins and lipids, trafficking

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6
Q

Mitocondria and what are their functions?

A

Outer and inner membrane and matrix.

Mitochondria are involved in making ATP, signaling, cell differentiation, and cell death.

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7
Q

What are lysosomes and what is their function?

A

Lysosomes contain digestive enzymes that degrade organelles and biomolecules

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8
Q

What are peroxisomes and what is their function?

A

Peroxisomes are small vesicular compartments that contain enzymes used in oxidation reactions

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9
Q

What are the three topological compartmentalization categories?

A
#1 Nucleus and cytosol -(communicate through nuclear pore complex)
#2 Organelles in secretory and endocrine pathways (ER, Golgi apparatus, endosomes, and lysosomes) - (Communicate through vesicles)
#3 Mitochondria
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10
Q

What does membrane budding and fusion allow topological equivalent organelles to do?

A

communicate with each other and with the cell exterior

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11
Q

Rough Endoplasmic Reticulum

A

-Parallel sacks of flat, elongated cisternae, studded with ribosomes.
-Functions include:
Protein modification and assembly
Segregation of proteins for intracellular use
Export from cell (ciollagen, cell membrane proteins)

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12
Q

What do cells that make secreted proteins have a lot of?

A

Rough ER

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13
Q

The mechanism by which secretory proteins are directed to the ER is explained by the what?

A

Signal sequence

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14
Q

In what do most proteins exit the RER and where are they usually transported to?

A

Most proteins leave in vesicles and are transported to the cis portion of the Golgi apparatus

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15
Q

How does the SER differ from the RER

A

The SER lacks ribosomes and has tubular cisternae

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16
Q

What are important functions of the SER

A

glycogen metabolism, lipid synthesis, phospholipid synthesis, detoxification, steroidogenesis, calcium regulation

17
Q

Where do the cis and trans section of the golgi apparatus face?

A

Cis is adjacent to the endoplasmic reticulum

Trans points to the plasma membrane or the nucleus

18
Q

What are the functions of the golgi apparatus?

A
  • modification of carbs
  • polysaccharide and oligosacchride synthesis
  • synthesis of sphingomycin and glycosphingolipids
  • Sorting of secretory products (marking w/ M6P)
  • packing ans storing secretory products
19
Q

When does the golgi apparatus disassemble? and reassemble?

A
  • disassembles during mitosis/meiosis

- reassembles in interphase

20
Q

Clathrin-coated vesicles

A

transport products from GOLGI to lysosomes

*seen in exocytosis/secretory and endocytosis pathway

21
Q

COP-coated vesicles

A

transport products between stacks of golgi apparatus and from ER to golgi apparatus

22
Q

What couses vesicles to pinch off from the plasma membrane

23
Q

Primary lysosomes

A

the storage site of lysosomal hydrolases.

  • no digestive events
  • homogeneous
  • inactive enzymes
24
Q

Secondary lysosomes

A

Engaged in catalytic process

  • digestive enzymes
  • heterogeneous
  • active enzymes
25
What are the three pathways for intracellular degradation?
Phagocytosis, autophagy, receptor-mediated endocytosis
26
Endocytosis
Lysosomes digest material taken up from outside the cell
27
Peroxisomes (microbodies)
organelles that are found in the cytoplasm of almost all cells, roughly spherical, and bound by a single membrane
28
what is the function of peroxisomes
- synthesis and degradation of hydrogen peroxide, - beta-oxidation of long chain fatty acids - bile acid and cholesterol synthesis - detoxify alcohol
29
What are Zellweger spectrium disorders
They are peroxisome biogenesis disorders | -caused by defects in the assembly of the peroxisome
30
Zellweger syndrome
characterized by an absence or reduced number of peroxisomes in the cells
31
What are mitochondria often associated with?
microtubular cytoskeleton
32
What do the enzymes within peroxisomes form?
They form hydrogen peroxide (can damage cell) which is immediately broken down by catalase