Microfilaments Flashcards

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1
Q

What does the bacterial cytoskeleton contain ?

A

Proteins that are homologous in structure to eukaryotic actin and tubulin and also other protein classes, possibly including intermediate filaments

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2
Q

What does the hydrolysis of ATP destabilise ?

A

The actin polymer

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3
Q

When does treadmilling occur ?

A

Treadmilling occurs with actin, where monomers are added at the plus end and lost at the minus end

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4
Q

What does dynamic instability involve ?

A

Dynamic instability involves a switch from growth to shrinkage (or opposite) at the plus end

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5
Q

What does alpha actinin help with ?

A

To create a scaffold

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6
Q

Explain the function of Profilin ?

A
  • Prevents globular actin from nucleating (ie forming new filaments)
  • Binds to ATP bound globular actin
  • Enhance formation of longer filaments
  • Replenish the pool of ATP–actin monomers by increasing the rate of nucleotide exchange on the bound actin monomer 1000-fold compared with the rate of exchange based on simple diffusion
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7
Q

Explain the function of Cofilin ?

A
  • Severs microfilaments

- Helpful when filaments need to be broken up and monomers recycled

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8
Q

Cell Migration via Lamellipodium

A
  1. Polymerisation of actin at the leading edge PUSHES plasma membrane forward (PROTRUSION) forming new actin cortex regions
  2. New anchor points are made between cell & substratum – via integrins
  3. As new anchorage sites are made at the front, some at the back are released (using myosin & actin interactions)
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9
Q

What is Lamellipodia ?

A

Based upon a thin sheet-like branched network of actin filaments

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10
Q

What is Filopodia ?

A

They are highly organised and tightly cross-linked long bundles of unidirectional and parallel actin filaments

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11
Q

What does the resulting branching structures push?

A

The plasma membrane forward. The plus ends of the actin filaments become protected from depolymerising by capping proteins (dark green), while the minus ends of actin filaments nearer the centre of the cell continually disassemble with the help of depolymerising proteins

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12
Q

Because of this directional growth and disassembly, individual actin monomers?

A

Accumulate at the rear, while the web of actin as a whole undergoes a continual forward movement

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13
Q

Nucleation of new actin filaments (pink ) is mediated by ?

A

ARP (Actin Related Protein) complexes (light green) attached to the sides of preexisting actin filaments

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14
Q

Myosin-I has a ?

A

Single globular head that attaches to an actin filament and a tail that attaches to another molecule or organelle in the cell

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15
Q

What does this arrangement allow ?

A

The head domain to move a vesicle relative to an actin filament, which in this case is anchored to the plasma membrane

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16
Q

Myosin-I can also bind to ?

A

An actin filament in the cell cortex, ultimately pulling the plasma membrane into a new shape

17
Q

Activation of Rho family GTPases can have a dramatic effect on ?

A

The organisation of actin filaments in fibroblasts

18
Q

A small, bipolar myosin-II filament can slide two ?

A

Actin filaments of opposite orientation past each other

19
Q

Skeletal muscle contraction is triggered by?

A

The release of Ca2+ from the sarcoplasmic reticulum into the cytosol

20
Q

a Ca2+-release channel in the sarcoplasmic reticulum membrane is opened by ?

A

A physical linkage to a voltage-gated Ca2+ channel in the T-tubule membrane

21
Q

Skeletal muscle contraction is controlled by?

A

Tropomyosin and troponin complexes

22
Q

Cross section of the muscle actin filament reveals how ?

A

Ca2+ binding to the troponin complex (not shown) leads to movement of tropomyosin away from the myosin-binding site

23
Q

Actin exists in a ? and what is it called ?

A

Monomeric form (g) and polymer form (f) and the polymer is called a ‘microfilament’

24
Q

Actin interacts with partner proteins including

A
  1. Myosin

2. And cofactors that stabilise or destabilise the polymers

25
Q

Actin is responsible for a lot of cellular movement including

A
  1. Phagocytosis
  2. Muscle movement
  3. Cytokinesis
  4. Cell migration