DSA Organelles Flashcards

1
Q

The outer boundary of cells is the _

What are its functions?

A

Plasma Membrane

Protective barrier, Transportation, Signaling

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

This organelle contains the genome.

It is the principial site for what?

A

Nucleus

DNA and RNA synthesis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

This consists of the cytosol and cytoplasmic organelles

A

Cytoplasm

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What is the difference between the two types of Endoplasmic Reticulum (ER)?

What is it involved with?

A
  • Rough ER has ribosomes attached to it, Smooth ER has no ribosomes
  • Protein and Lipid synthesis, Protein folding, and Calcium storage
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

This organelle is stacks of disc like compartments

What is it involved with?

A

Golgi Apparatus

Post-Transitional Changes and Protein Trafficking

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Functions of the Mitochondria

A

Making ATP

Signaling

Cell Differentiation

Cell Death

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

This organelle contains digestive enzymes that degrade organelles and biomolecules

A

Lysosomes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

This organelle has small vesicular compartments that contain enzymes used in oxidation reactions

A

Peroxisomes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

The cell is divided into 3 Topological categories

A
  • Nucleus and cytosol
    • Communicate through nuclear pore complex
  • Organelles in secretory and endocytic pathways (ER, Golgi Apparatus, Endosomes, Lysosomes)
    • ​Communicate though vesicles
  • Mitochondria
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Topologically Equivalnet Organelles

What allows the lumen of these compartments to communicate with each other and with the cell exterior?

A

Membrane budding and fusion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

The ER divides the cytoplasm into two compartments

A

Luminal (cisternal compartment) & Cytoplasmic (cytosolic compartment)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Rough ER

What makes this organelle unique from Smooth ER?

What type of cells have lots of RER?

A

Presence of ribosomes

Cells that make secreted proteins

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

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

A

Signal sequence

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Most proteins exit the RER in vesicles transported to where?

A

Cis portion of the Golgi apparatus

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Smooth ER

Different from RER in what two ways?

Important functions include?

It is abundant in cells that make what?

A

Lacks ribosomes and has tubular cisternae

Lipid & Phospholipid Synthesis, Detoxification

Cells that make steroids or lipids

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Golgi Apparatus

What are the two distinct faces and what structures do they face?

A

Cis-Golgi (entry face) is adjacent to ER

Trans-Golgi (exit face) points toward plasma membrane

17
Q

Golgi Apparatus Functions

A
  • CHO modification attached to glycoproteins and proteoglycans
  • Poly- and oligosaccharide synthesis
  • Sphingomyelin and glycosphingolipid synthesis
  • Sorting Secretory Products
    • Ex: Marking lysosomal enzymes with M6P
  • Packaging/Storing Secretory products into secretory granules/vesicles
18
Q

Vesicular transport mechanism involves two types of coated vesicles:

_ transport products from Golgi apparatus to lysosomes or products from the exterior of the cell to the lysosomes

_ transport products between stacks of Golgi apparatus and from the ER to the Golgi apparatus

A

Clathrin-Coated Vesicles

COP-Coated Vesicles (Coat Protein)

19
Q

Clathrin-Coated Vesicles

Which pathways are they involved with?

What surrounds the neck of the invaginated coated pit, causing the neck of the vesicle to pinch off from the PM?

A

Exocytosis/Secretory and Endocytosis pathways

Dynamin

20
Q

Lysosomes

Organelle that contains 50-60 hydrolytic _ that are capable of breaking down proteins, CHO, lipids, and nucleic acids

A

Enzymes most active at acidic pH

21
Q

What do Lysosomes have that maintain acidic intralysosomal environment?

A

ATP-dependent H+ pump

22
Q

What are Primary Lysosomes? Secondary Lysosomes?

A
  • Primary: Storage site of lysosomal hydrolases
    • No digestive events, inactive enzymes, homogenous
  • Secondary: Engage in catalytic process
    • Digestive, active enzymes, Heterogenous
23
Q

What are 3 pathways for intracellular degradation?

A

Phagocytosis (Cell/Particle)

Autophagy (Damaged organelle)

Receptor mediated endocytosis (Macromolecules)

24
Q

How are lysosomes formed?

How do early endosomes mature into late endosomes?

What is the important change in endosome maturation?

A

Fusion of transport vesicle with endosome (contain molecules taken up by endocytosis)

Clathrin components recycled and early endosomes mature into late endosomes (precursor of secondary endosome)

Lowering of internal pH to 5.5

25
Q

Peroxisomes contain number of enzymes that form _ which is immediately broken down by _

What is its function?

A
  • Hydrogen Peroxide broken down by Catalase
  • Functions:
    • Hydrogen Peroxide Synthesis/Degradation
    • B-Oxidation of LCFAs
    • Bile Acid and Cholesterol Synthesis
    • Detoxify Alcohol
26
Q

Peroxisome biogenesis disorders that are caused by defects in the assembly of the peroxisome

A

Zellweger Spectrum disorders

27
Q

Mitochondria make up _% of the cytoplasmic volume

How can mitochondrial diseases arise?

A

20%

Mutation in the mtDNA that affect mitochondrial function or mutations in genes of nuclear DNA whose products are imported as mitochondria proteins

28
Q

Mitochondrial diseases are sometimes caused by mutations in the _ that affect mitochondrial function

A

Mitochondrial DNA