Cytoskeleton Flashcards

1
Q

Why do cells need a cytoskeleton

A

Cells need to be strong and dynamic

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2
Q

Why don’t plant cells move

A

Because they have a cell wall

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3
Q

What are the 3 core filament proteins in the cytoskeleton

A

Actin microfilaments
microtubules
Intermediate filaments

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4
Q

What is this a cross section of

A

Actin microfilament

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5
Q

What is this a cross section of

A

Microtubule
Around 25nm in diameter

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6
Q

What is this a cross section of

A

Intermediate filaments

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7
Q

What are the characteristics of actin microfilaments

A
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8
Q

What are the characteristics of microtubules

A
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9
Q

What are the characteristics of intermediate filaments

A
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10
Q

Label this diagram of an actin microfilament

A
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11
Q

Actin Microfilaments :

A
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12
Q

Mictrotubules:

A
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13
Q

Intermediate filaments:

A
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14
Q

Why are filaments used for strength in a cell

A
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15
Q

Why are filaments made up of subunits

A
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16
Q

What is the structure of intermediate filaments and how is its structure formed

A
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17
Q

What happens if something goes wrong with intermediate filaments

A

Lead to disease e.g amyotrophic lateral sclerosis

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18
Q

What are the characteristics of the bacterial cytoskeleton

A
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19
Q

What are some different examples of microfilaments in a cell and what do they do

A
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20
Q

What are the characteristics of actin

A
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21
Q

What characteristic does microfilaments have

A

They are dynamic

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22
Q

What are the phases of dynamic filament

A
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23
Q

What is the critical concentration

A
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24
Q

What is nucleation needed for

A

Neede to facilitate growth
It brings G actin together to form oligomers

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25
Q

Using a diagram, describe the process of treadmilling

A
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26
Q

What is treadmilling

A
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27
Q

What happens when ATP vinds to actin

A

The conformation of actin changes
This changes the affinity in the filament

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28
Q

What is the rate of ATP/ADP addition at the plus and minus ends of the microfilament

A

Rate of ADP addition is slower than ATP addition at both ends of the microfilament
ADP not readily added to the plus end
The rate if loss of ADP actin is greater than the rate of addition of ATP at the minus end, but at the plus end loss of ADP actin is faster than at the minus end

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29
Q

Where does ADP actin tend to end up in a microfilament

A

Tends to end up in older parts of the filament

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30
Q

Using a diagram, explain the concept of critical concentration

A

Treadmilling occurs when the concentration of free subunits is between the critical concentrations for the two ends

Plus End Critical Concentration :The concentration of monomers required for polymerization at the plus end.
Minus End Critical Concentration : The concentration of monomers required for polymerization at the minus end

Is above Cc+, the filament will grow at the plus end.
Is below Cc- , the filament will shrink at the minus end.
Is between Cc+ and Cc- , treadmilling can occur, where the filament grows at the plus end and shrinks at the minus end.

Critical Concentration: Describes the equilibrium concentration of free monomers required for no net growth or shrinkage at a filament end.

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31
Q

What are nucleators and why are they needed

A

Nucleators are proteins or complexes that facilitate the formation of new actin filaments or microtubules, a process known as nucleation

They are needed because spontaneous nucleation takes too long (as it relies on diffusion)

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32
Q

What are the two main types of nucleators and what are their main roles

A
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33
Q

What is the role of ARP 2/3

A

ARP= actin related proteins
They can act as a starting point for nucleation as they have a similar structure to Actin

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34
Q

How does ARP 2/3 help produce microfilaments

A

It holds the minus ends and allows the plus ends to grow

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35
Q

Why is growth of the branches (daughter filaments) important for a cell

A

They produce a force that pushes the plasma membrane forward at the leading edge of motile cells
(Cells need it to move)

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36
Q

What is the role of formins

A

They provide a template for the growing plus ends of microfilaments
2 actin subunits are held by formin

37
Q

How does formin work to help nucleation/ filament formation

38
Q

What are actin binding proteins and what do they do

39
Q

What are the proteins involved in controlling the growth of microfilaments

40
Q

What are filament severing proteins and what do they do

41
Q

What is the role of filamin

42
Q

What do filament binding proteins do. Name two types and what they do

43
Q

What is the role of microtubules

44
Q

What is the structure of microtubules

45
Q

How does microtuble nucleation occur

46
Q

What is the microtubule organising centre

47
Q

How are microtubules organise themselves from the centrosome

48
Q

What do centrosomes contain

A

-they contain a centriole pair

49
Q

What are microtubules able to do if they are severed from their centriole

50
Q

How does microtubule treadmilling work

51
Q

What is dynamic instability and how does it occur

A

involves the rapid switching between phases of microtubule growth (polymerization) and shrinkage (depolymerization).

Beta tubulin binds GTP before polymerizing onto the growing end of a microtubule.
The β-tubulin subunit of the dimer hydrolyzes GTP to GDP after incorporation into the microtubule lattice.
Tubulin bound to GTP (GTP-tubulin) is more stable and promotes microtubule growth, while tubulin bound to GDP
(GDP-tubulin) is less stable and promotes depolymerization

A growing microtubule typically has a “GTP cap” at its plus end (the rapidly growing end), where GTP-tubulin dimers are added faster than GTP is hydrolyzed to GDP.
The presence of this GTP cap stabilizes the microtubule and promotes further growth.

If the rate of GTP hydrolysis exceeds the rate of GTP-tubulin addition, the GTP cap is lost, exposing GDP-tubulin. This destabilizes the microtubule and leads to rapid depolymerization or shrinkage.
Rescue: The switch from shrinkage to growth can occur if enough GTP-tubulin dimers are incorporated to re-establish the GTP cap, stabilizing the microtubule and allowing it to start growing again.

52
Q

Draw a diagram to represent how dynamic instability and catastrophe occurs

53
Q

Draw a graph to show how length of the microtubule varies over time

54
Q

Why may dynamic instability be useful for a cell

55
Q

What are 2 types of microtubule binding proteins and what do they do

56
Q

What does MAP2 and tau do

57
Q

How is tau targeted in Alzheimer’s

58
Q

What are microtubule stabilising proteins and give an example

59
Q

What do katanins do

A

Makes disassociation of microtubules more likely

60
Q

How does katanin work

61
Q

What drugs can be used to perturb the cytoskeleton

62
Q

How can cell wall formation be guided by microtubules - draw a diagram to help explain this

63
Q

What is the role of microtubules in cell division

64
Q

Why is diffusion not enough for transport around the cell

65
Q

What are the 3 main classes of motor proteins

66
Q

How are energy and force produced for motor proteins

67
Q

What kind of motor protein does prokaryotes have

A

They have a bacterial flagella

68
Q

What are the 2 ways in which motor proteins are anchored

A

If elastic force exceeds resistance the track or motor will move (depending on which is anchored)
So if motor is anchored the track will move and vice Vera’s

69
Q

What structures are conserved in motor proteins

70
Q

Which class of motor protein is this

71
Q

What class of motor protein is this

A

Cytoplasmic dynein

72
Q

What class of motor protein is this

73
Q

How do kinesins and dyneins work

74
Q

Describe the structure of kinesins

75
Q

Describe the structure of dynein

76
Q

How do dyneins move across microtubules

A

As dynein-1 moves along an MT, ATP hydrolysis in the AAA+ ring of each monomer generates a series of conformational changes, which detach the monomer from the MT and reorient its linker domain to produce a net step toward the minus end

77
Q

What is the function of dyneins

78
Q

What is this a cross section of

79
Q

How do ciliary dyneins cause the cilia to bend

80
Q

How does dynein and Kinesin work together

81
Q

Draw a diagram to show how kinesins and dyneins work in a cell

82
Q

How does influenza hijack the cytoskeleton

83
Q

What are the characteristics of the myosin superfamily

84
Q

What is the structure of myosin

85
Q

How do myosin motors produce force and move along the actin filament

86
Q

What is the structure of actin and myosin in muscles

87
Q

What happens when myosin goes wrong

88
Q

What is the role of myosin motors in cell division