Organelles Flashcards

1
Q

What are some benefits of having distinctive organelles in a eukaryotic cell?

A

Membrane-bound spaces permit the segregation of functions within the cell and the concentration of specific functions. organization of protein movement through the cell. Both facilitate increasing levels of complexity found in eukaryotes. Another key function is to facilitate degradation of worn-out cell components in the longer-lived eukaryotes. The same degradative system can be modified to process extracellular material.

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2
Q

What is the major benefit of having membrane-bound organelles?

A

Organelles increase membrane surface area, maintain specificity and complexity of function

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3
Q

Which organelles are not membrane bound?

A

Ribosomes and proteasomes are macromolecular complexes.

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4
Q

What is the function of mitochondria?

A

Powerhouse of cell. Produces ATP through the electron transport chain and citric acid cycle.

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5
Q

Describe process of ATP generation in mitochondria

A
  1. Electron goes through 3 complexes, pumping out H+ out of matrix (creates gradient). ATP synthase rotates due to gradient change, driving ATP synthesis
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6
Q

What is the function of the Golgi?

A

The Golgi apparatus consists of stacks of flattened vesicles that have been likened to pita bread. Proteins from the ER are modified (e.g. glycosylation) and then sorted to their various specific final locations.

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7
Q

About what proportion of cells are within the membrane bound organelles? Which, are the largest?

A

Cytosol 50%; Mitochondria- 20%; Golgi and ER: 15%; nucleus 6%; rest take up small portions

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8
Q

Where are most of the proteins involved in ATP generation located?

A

The inner mitochondrial membrane (which is folded into christae) contains the proteins of the electron transport system and the enzyme ATP synthase.

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9
Q

What is the driving force for ATP synthesis?

A

The electrochemical gradient of hydrogen ions in the intermembrane space, created by the electron transport system, is the driving force that activates ATP synthase.

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10
Q

What is the role of the two components of the ribosomal complex?

A

The small subunit binds mRNA, which then binds to the large ribosomal unit. The large ribosomal unit has three sites (A-site, P-site and E-site) for binding of tRNAs

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11
Q

What is the function of the smooth ER?

A

Synthesis of membrane lipids (phospholipids, cholesterol and glycolipids), synthesis of steroid hormones, drug detoxification (cytochrome p450 enzymes) and sequestration of calcium.

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12
Q

How does protein know to go into the endoplasmic reticulum?

A

There is a signal recognition particle (SRP) that recognizes a signal sequence on the beginning of the developing protein. This particle binds to the endoplasmic reticulum and the forming protein is inserted through the membrane of the endoplasmic reticulum, where it folds.

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13
Q

What kinds of proteins are inserted into the endoplasmic reticulum?

A

Secreted proteins and proteins that become associated with the membranes of the cell surface or other organelles.

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14
Q

Why do ribosomes represent an important target of antibiotics?

A

Prokaryotes (such as bacteria) have different ribosomal subunits which can be targeted by specific chemicals (killing the bacteria and not damaging the eukaryotic cell).

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15
Q

What is the role of proteosomes and what would happen if these were not functional?

A

They degrade proteins attached to ubiquitin. This is used to recycle some normal proteins, but also to eliminate misfiled proteins. These proteins would accumulate in the cell if the system were not functional.

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16
Q

Can misfolded proteins be “fixed?

A

There are “chaperone proteins” that can aid in refolding by their interaction with the misfiled protein. This often does not work and the protein needs to be recycled.

17
Q

How do things transit through the Golgi apparatus?

A

They transit from the cis-face to the trans-face by vesicular transport between the cisterns.

18
Q

What marker on the membrane is most important in moving vesicles from the RER to the Golgi and from the cis Golgi through the cistern to the trans Golgi? What marker is present on vesicles moving in the other direction?

A

COPII (coat protein II) is present on things moving from the RER and from cis to trans faces. COPI is present on vesicles moving retrogradely.

19
Q

What are the three main categories of vesicles budding off of the trans-Golgi face?

A

Lysosomes, secretory vesicles, and vesicles fusing with the surface membrane.

20
Q

What is the tag on enzymes destined for inclusion in the lysosomes?

A

Mannose 6-phosphate.

21
Q

What functions take place in the cis Golgi? The medial Golgi cisterns? The trans Golgi cisterns?

A

In the cis Golgi cisterns, N-linked oligosaccarides are trimmed and other sugars added. In the medial Golgi cisterns there is glycosylation of some lipids and serene and threonine residues. Also, there is further modification of N-linked oligosaccarides. In the trans Golgi cisterns, sialic acid is added to some carbohydrates along with sulfation of tyrosine and some sugars.

22
Q

What is the function of a peroxisome?

A

They contain enzymes involved in the beta-oxidation of long-chain fatty acids, detoxification (including alcohol) and synthesis of plasmalogens (mostly in myelin of nerves). Oxydation results in generation of hydrogen peroxide.

23
Q

What happens with deficiency of specific acid hydrolases in lysosomes?

A

There is accumulation of the product that can’t be broken down (and often cell death).

24
Q

What is the function of autophagocytosis?

A

Recycling old, worn out organelles within the cell.

25
Q

What blocks the A site of ribosomes?

A

Tetracyclines

26
Q

What blocks the peptidyl transferase reaction of ribosomes during translation?

A

Chloramphenicol

27
Q

What blocks the exit channel of ribosomes during translation?

A

Erythromycin

28
Q

What is I-cell disease?

A
Inclusion bodies on histo slides
Lipids not broken down; results from a defective enzyme in Golgi --> lysosomal proteins cannot be targeted to lysosomes correctly so bad stuff can't be broken down in the lysosomes
Coarse facial features
Skeletal abnormalities
Mental retardation
Fatal by 7yo