Scaffold of the cell Flashcards

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1
Q

What are the3 major types of protein filament in the cytoskeleton?

A
  • actin microfilaments
  • tubulin microfilaments
  • intermediate filaments
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2
Q

What are the roles of microtubules in cells?

A
  • maintain cell shape
  • swimming and surface movement of fluids
  • formation of the mitotic spindle
  • tracks for movement of vesicles organelles, proteins
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3
Q

What is tubulin?

A

-a dimer made out of α and beta tubulin subunits

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4
Q

What can each dimer of tubulin bind to?

A

2 GTP molecules

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5
Q

What gives tubulin polarity?

A

the GTP on beta tubulin being hydrolysed

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6
Q

How does the polymerisation of microtubulins occur?

A
  1. tubulin monomers from dimers
  2. the dimers polymerise into oligomers
  3. oligomers grow into linear protonfilaments and Mts
  4. MTS elongate reversibly by adding dimers. Dimers attach to both ends of Mts but preferably at + end
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7
Q

what is an MTOC?

A

microtubule organising centre formed from enucleated microtubules

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8
Q

How is the structure of microtubules?

A

13 Tubulin fillaments in a hollow ring

Plus end = Beta subunit
Minus end = Alpha subunit

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9
Q

Describe the growth of MTs?

A

Have dynamic instability

microtubules may grow steadily and then shrink rapidly by loss of tubulin dimers from the + end

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10
Q

What are the two classes of microtubule binding drugs?

A

tubulin dimer binding - Vinblastine

tubulin polymer binding - Taxol

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11
Q

What does the action of the dimer binding microtubule drugs tend to be?

A

inhibit polymerisation

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12
Q

What is an example of a polymer binding microtubule drug and what is its action?

A
  • taxol

- favours polymerisation

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13
Q

What are MT binding drugs used as?

A
  • anti-mitotic agents

- anti-cancer agents

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14
Q

What is taxol used to treat?

A

ovarian carcinomas and advanced breast carcinomas

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15
Q

What is vinblastine/viscristine used to treat?

A

-Hodgkin’s disease
-lymphocytic lymphoma
histiocytic lymphoma
-advanced testicular cancer
-advanced breast cancer
-Kaposi’s sarcoma

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16
Q

What are microtubule-associated proteins (MAPs)?

A

a family of proteins that bind to and stabilise microtubules

17
Q

What is the function of MAPs?

A
  • MAPs binding speeds up polymerisation, facilitates MT assembly and stabilises the microtubules
  • the other end projects outing will bind to vesicles, actin or other MTs
18
Q

What is MAP function regulated by?

A

phosphorylation

19
Q

What are some features of microtubules?

A
  • thickest of cytoskeletal filaments
  • 2 tubulin isoforms: alpha and beta
  • GTP dependant assembly
  • long hollow cylinders made up of 13 protofilaments
  • dynamically unstable
  • attach to microtubule organising centres
  • ovement of organelles and vsicles, cell division
20
Q

What are the roles of actin filaments in cells?

A
  • maintenance of cell shape
  • cell movement of chemotaxis
  • interaction of environment
  • tracks for movement of vesicles, organelles, proteins etc
21
Q

What are the actin filament locations in cells?

A
  • microvilli
  • adhesion belt
  • cell cortex
  • filopodia
  • lamellipodium
  • stress fibres
  • contractile ring
22
Q

What are the three types of actin?

A

α-actin
beta actin
gamma actin

23
Q

What can a monomer of actin bind to?

A

one molecule of ATP or one molecule of ADP

24
Q

How do the actin subunits arrange themselves?

A

the subunits are polar and assemble head to tail with one another

25
Q

What are the stages of actin polymerisation in vitro?

A
  1. nucleation (lag phase) actin subunits form oligomers
  2. elongation (growth phase) actin filaments grow
  3. steady state (equilibrium phase) actin filament with subunits coming on and off
26
Q

What drugs work on actin and how do they work?

A

Phalloidin (stabilises F-actin by locking adjacent subunits together which kills the cell)

Cytochalasin (binds the barbed end of F-actin and prevents polymerisation)

Latrunculin (binds to actin monomers and prevents them from being added onto filaments)

27
Q

What does actin polymerisation provide?

A

a force for cell movement

28
Q

How is actin arranged?

A

organised into many different patterns (2D and 3D patterns)

29
Q

How many actin isoforms are there and where are they found?

A

6
4 in muscle
2 in cytoskeleton

30
Q

What are the difference in mechanical properties of IFs, AFs and MTs?

A
  • MTs are deformable but unable to withstand force
  • actin filaments can withstand moderate force but are not easily deformed
  • IF are able to withstand high forces and are highly deformable
31
Q

What are some features of IFs?

A

-intermediate in size
-nuclear filaments-lamins
-others specific to cell type
mechanical stability-twisted coils

32
Q

What is a key concept to remember about the cytoskeleton?

A

It is dynamic