cell cytoskeleton Flashcards

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1
Q

Explain the importance of the cytoskeleton.

A

Network of protein filaments
- Very dynamic, responds to environment quick
- Important in cell shape, interior organisation and movement

  • Support cell
  • Maintain shapes
  • Holds organelles in position
  • Movement of cytoplasm
  • Interacts with extracellular structures, anchors cell in place
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2
Q

Compare and contrast microfilaments, microtubules, and intermediate filaments in terms of structure and function. MICROFILAMENTS

A

microfilaments
- smallest in diameter
- made of globular actin proteins
- actin proteins bind to form helical polymers
- two helical polymers form microfilament
- twisted chain diameter is 7nm
- long, thin and very flexible

  • polarized structures
  • have +/- end, grow quick at + end
  • allow actin monomers to interact with each other to form helical chains
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3
Q

Microfilaments polymerization and depolymerization

A
  • have +/- end, grow at + end, lost from minus end
  • polymerization of actin into microfilaments is reversible
  • hydrolysis of ATP determines polymerization and depolymerization
  • when bound to ATP, actin has high affinity for other actin molecules and binds tightly to them
  • when hydrolyzed to adp, affinity decreases
  • microfilaments break down into monomers of free actin

high concentration –> growth of filament, rate of addition higher than loss

intermediate concentration (tread milling) –> equal growth and loss, filament stays the same length
- loss from - add, add app come back on + end, actin filament is moving in one direction, direction of movement

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4
Q

Microfilaments and actin-binding proteins

A
  • actin binding proteins control organization of actin filaments
  • can exist as, single, linear bundles, 2D networks, 3D gels

stability
- stabilizes microfilament from depolymerizing
- side-binding, prevents branching

organization
- bundling and cross linking proteins involved organization

  • nucleating protein helps polymerization

function and movement
- motor proteins, can walk on microfilaments MYOSIN, vesicle transport and muscle contraction

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5
Q

Explain the cellular processes in which each filament is involved: MICROFILAMENTS

A
  • highly concentrated in cortex beneath cell membrane, in contact with plasma membrane

2 major roles:
- cell stability and shape
- cell movement

in non muscle cells, associated with cell shape

  • microvilli
  • contractile bundles in cytoplasm
  • fingerlike filopodia in moving cell
  • contractile ring during cell division

cell shape- cell division
- pinch contraction of middle of cell, 2 daughter cells into 1, through myosin proteins

cell movement
- form cellular extensions called filopodia pseudopodia

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6
Q

Cellular process: CELL SHAPE AND MICROFILAMENTS

A
  • epithelial cells
  • line intestine to increase absorption have microvilli to increase surface area
  • microvilli supported by microfilaments

-cross linking actin binding proteins form netlike structure of microfilaments

  • interact with intermediate filaments at base of each microvilli which helps stabilize microvilli
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7
Q

Cellular process: VESICLE MOVEMENT AND MICROFILAMENTS

A

movement of vesicle inside cell:

  • microfilament attached to plasma membrane
  • myosin motor proteins walk on microfilament carrying vesicles
  • bring it to plasma membrane

contraction of membrane

  • myosin motor protein attached to membrane
  • one side attached to membrane, other side to microfilament
  • movement of protein takes microfilament (and all other microfilaments associated with it) in one direction
  • pinching during cell division
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8
Q

Cellular process: MUSCLE CONTRACTION AND MICROFILAMENTS

A
  • different class of myosin (II)
  • moment of myosin on microfilaments brings them together
  • actin filaments slide against myosin during muscle contraction
  • acetylcholine detected, calcium increases in cytoplasm, protein that hide binding site removed through changes in conformation, now myosin can walk on actin and bring myosin filaments closer together
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9
Q

Cellular process: CELL MOVEMENT AND MICROFILAMENTS

A

SEE DIAGRAM

  • dynamic properties + motor proteins
  • cell receives signal, in response changes cytoskeleton to move in direction of source of signal

extension

  • at leading edge, actin polymerization pushes plasma membrane forward (protrusion) and forms new region of actin cortex

adhesion
- new anchors made between bottom of cell and surface, substratum, on which its crawling (attachment)

translocation
- depolymerization and contraction at the other end of the cell due to myosin moving along actin filaments draws cell body forward

de-adhesion
- new anchor points made at front, old released at back

  • cycle is repeated
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10
Q

Compare and contrast microfilaments, microtubules, and intermediate filaments in terms of structure and function. INTERMEDIATE FILAMENTS

A

intermediate filaments

  • tough and rope like
  • very flexible
  • tensile strength
  • made of FIBROUS proteins
  • resist mechanical stress (skin cells)
  • more permanent structures, do not rupture under stress but deform
  • more structural support than movement

structure
- long twisted strands of protein
- monomer is alpha helical
- 2 monomers is dimer
- 2 dimer bind laterally to make tetramer
- 8 tetramer interact laterally and now are ready to be added to growing filament
- make rope like structure

4 major classes
- not different in amino acid but terminal sites, bind different proteins

cytoplasmic

  • KERATIN: epithelial cells
  • VITEMIN: connective tissue, muscle, glial cells
  • NEUROFILAMENT: nerve cells

nuclear
- NUCLEAR LAMINS: in all animal cells

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11
Q

Cellular process: INTERMEDIATE FILAMENTS AND MECHANICAL STRENGTH AND CELL SUPPORT

A
  • create strong durable network in cytoplasm

some types:
- form meshwork called nuclear lamina beneath inner nuclear membrane to support and strengthen nuclear envelope

other types:

  • extend across cytoplasm
  • bind 2 parts of the cell, desmosomes are where 2 neighbouring cells bind each other (from one junction to another)
  • intermediate filaments bound to plasma membrane at level of desmosomes
  • collection of intermediate filaments connect cell together allows it to stretch
  • give mechanical strength to cells and distribute mechanical stress in epithelial tissues
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12
Q

Compare and contrast microfilaments, microtubules, and intermediate filaments in terms of structure and function. MICROTUBULES

A
  • rigid hollow tubes
  • need organization centre to grow from, centrosomes
  • made of tubulin dimer which has 2 GLOBULAR subunit tubulin proteins: alpha and beta
  • 13 protofilaments of tubulin
  • several micrometers long
  • more rigid, ruptured when stretched
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13
Q

Microtubule polarization, centrosomes and dynamic instability

A

polarization:
- have +/- end
- addition of tubulin (alpha beta dimer) to + end

centrosomes:
- need organizing centre to grow from
- centrosomes have rings to which alpha and beta tubulin proteins are added
- minus end is inside centrosome connected to ring
- + end extends into cytosplasm
- microtubules grow and shrink fast INDEPENDENT of one another

dynamic instability:
- switching back and forth between polymerization and depolymerization

growing
- subunits of microtubules bind gtp have high affinity for one another
- grow towards positive side

shrinkage
- if addition of tubulin is slow
- hydrolyze gtp and lose affinity for each other
- not tightly packed together
- depolarization from + end happens

very fast
- once gtp is lost, nothing prevents microtubule from depolarization
- add gtp quick to regrow

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14
Q

Microtubules and microtubule binding proteins

A
  • plus end initially free but binds to specific protein which help stabilizes it
  • minus end protected by centrosome
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15
Q

Explain the Cellular processes: STRUCTURAL AND FUNCTIONAL ROLES

A
  • form rigid internal skeleton
  • framework along which motor proteins can move structures within cell
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16
Q

Cellular processes: MICROTUBULES AND MOVEMENT OF CYTOPLASMIC MATERIAL

A
  • transport vesicles, macromolecules and organelles
  • 2 types of motor proteins used
  • kinesins –> move material to +
  • dyneins –> move material to -
  • involved in movement of chromosomes in cell division
  • dynenin allows mictrotubules to slide past each other in cilia and flagella
17
Q

Microtubules and nerve cell transport

A
  • guide transport of organelles, vesicles and macromolecules in both directions along nerve axon
  • microtubules in axon point in same direction with + end towards axon terminal
  • bind to kinesin and take material and walk towards + end
  • back to cell body, bind to dynein taken to cell body to be destroyed (organelles, worn out mitochondria)
  • MORE EFFICIENT MOVEMENT OF MOVING ORGANELLES AND VESICLES INSTEAD OF JUST DIFFUSING
18
Q

Cellular processes: MICROTUBULES AND CHROMOSOME DIVISION

A
  • help distribute chromosomes in a dividing cell
  • in cell division, nuclear envelope breaks down and DNA is condensed into visible chromosomes
  • chromosomes duplicate to form conjoined pair which will be pulled apart into separate cells by microtubules
  • depolymerization of microtubules (shrink), chromosomes taken to either side of cell
19
Q

Cellular processes: MICROTUBULES AND ORGANELLE POSITIONING

A

DRAW DIAGRAM

  • help position organelles in eukaryotic cell
  • kinesin motor protein bind to membrane pull ER outward along microtubules
  • dynein motor protein bind membrane and pull Golgi apparatus inward along microtubule near centrosome
20
Q

Cellular processes: MICROTUBULES AND CILIA AND FLAGELLA MOVEMENT

A

SEE DIAGRAMS

  • cilia and flagella are moveable appendages on eukaryotic cells
  • cilia on surface of epithelial cells in resp tract, role of cilia is to move material on surface of cell (mucus moved to throat then swallowed)
  • flagella in sperm, way longer, role is to move entire cell
  • different size and function but same structure: microtubules arranged in different patterns
  • in all cilia and flagella (9+2 array)

-9 doublet to fused pairs of microtubules are arranged in ring
- surround single pair of unfused microtubules

  • motor proteins between microtubule doublets, moving along neighbouring microtubule to have bending and hair-like wave like movement
  • sliding of microtubule doublets past one another
  • driven by motor protein dynein which bind between 2 neighbouring microtubule pairs
  • as dynein changes shape, pairs move past each other
  • another protein nexis, limits how far they slide
  • inhibition of one side and activity of other causing bending,