cytoskeliton Flashcards

1
Q

size and function of microfillaments

A

5-7nm
Actin Determine cell shape
Allow cell movement

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2
Q

size and function of intermediate filaments

A

10-12nm
Intermediate filament proteins: large family of proteins
Mechanical strength and structure

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3
Q

size and function of micro-tubules

A

25 nm in diameter
Organelle and chromosome movement:
Determine position of membrane -bound organelles
Direct transport in the cell
Separate sister chromatids during cell division

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4
Q

actin micro-filaments are used to

A

1) alow dynamic movement e.g. chemo attraction fillapodia
2) define shape of cell e.g. growth cones fillapodia
3) pinching off of cell in cell division

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5
Q

explain how actin filament polarity contributes to function

A

G actin can polymerize at both - & + end but polymerizes faster at + end this is used to move actin in a controlled direction

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6
Q

Capping proteins can be used to create unidirectionality in actin explain:
Cap-z
Tropomodulin

A

Cap-Z blocks + end (normal growth end) limits growth to - end.
Tropomodulin blocks - end where it usually depolymerises stabilizing it for growth.

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7
Q

microtubule composition:

A
  • Polymers of Α and β tubulin forming dimers
  • dimers organised in protofilament chains (thermaly unstable)
  • multiple protofilaments organised round into 13 subunit tubes which are stable
  • can be connected into singlet dublets or triplets
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8
Q

microtubule assembly involes addition of

A

GTP bound beta tubulin

while GDp bound tubulin is removed

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9
Q

Cytoplasmic kinesin family members walk cargo along microtubules in which diection

A

towards + end away from centromere

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10
Q

dyenin members walk cargo along microtubules in which diection

A

towards - end towards centromere

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11
Q

properties of intermidiate fillaments

A
No intrinsic polarity
No nucleotide binding
No known motors
High stability
Unique to metazoans
Many different types: -Nuclear lamins -Keratin -Vimentin
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12
Q

keratin structure

A

Conserved alpha-helical rod domain that forms a coiled -coil motif.
then form protofillaments -pairs of coiled coils (simetric no polarity
these coil together to form microfibrils

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13
Q

Actin cytoskeleton basis of cellular movement in 3 main ways

A

Chemotaxis = movent response to chemical signal
Muscles
Flagelum

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14
Q

Actin also enables cells to crawl by:

A

assembling in growth direction and disassembling at other end.

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15
Q

Actin polymerisation drives envagination and phagocytosis by:

A

by ARP2/3 dependent actin polymerization around nucleation factors on cell surface

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16
Q

there are 3 main classes of myosin explain differences:

A
class 1 with a singular motor head. 
Class II and class v are diners class two often conjoining more= less flexibility often used in muscle
Class v can walk along an actin filament due to the splay of its motor head enabling e.g. vesicle transport
17
Q

eukaryotic flagellum consist of:

A

circular arrangement of micro-tubules with ATP dependent dyenin cross links that bend the flagellum

18
Q

structure and variation of actin filaments alpha beta and gama

A

Two stranded helical polymers of G-actin monomers

Alpha form in muscle, beta and gamma in other cells

19
Q

microtubules convert between growth and shrinkage GTP favours growth GDP favours shrinkage what is this called

A

dynamic instability

20
Q

Microtubules often radiate from organising centers (often centrosome) - stable minus end is embedded to prevent breakdown. examples include

A

Fibroblast: All microtubules head out from MTOC
Neuron axon: microtubule plus end at synapse; minus end in cell body
Transport down long axons; degeneration: starvation of axon terminals
Vesicles transported along microtubules at synapse

21
Q

(micro-tubules) tubulin mutations:

A

a-tubulin mutations cause impaired neuronal migration in mice and lissencephaly in humans (a brain development abnormality)
b-tubulin mutations cause cortical malformations in the brain

22
Q

intermediate filaments- Neurofilament proteins:

A

light, medium and heavy (NF-L, NF-M, NF-H) NF proteins form cross-links to provide axons with tensile strength The Level of NF gene expression controls axon diameter (structure), hence rate of electrical signal (function)

23
Q

intermediate filaments- Nuclear lamin proteins

A

Nuclear lamin proteins A, B and C Form nuclear lamina: meshwork of intermediate filaments lining inside of inner nuclear membrane Determines nuclear shape and provides anchoring point for chromosomes and proteins of nuclear pore complex. Lamin genes are the ancestral intermediate filament. Regulates nuclear reassembly after mitosis

24
Q

what are the 3 types of cell junction

A

adherant juctions- hold cells together
occluding junctions- seal the gap
gap junctions- alow transport/comunication
synapses

25
Q

adherent/anchoring junctions types

A

Desmosomes: cell to cell
Hemidesmosome: cell to basal lamia
adherins junction connects actin bundeles of two cells
desmosomes connect intermidiate fillaments of once cell to the next

26
Q

what family of protines hold two desmosomes together

A

cadherin family

27
Q

tight occlusion junctions
function:
Examples:

A

Control permeability between cells paracellular transport
Prevent proteins leaking into the interstitial fluid from capillaries or into bladder from glomerulous.
Barrier to ‘harmful’ luminal contents but allows uptake of nutrients/drugs
Permeability changes dependant on type of tissue small intestine vs blood brain barrier

28
Q

occlusion junction pathology

A

Pathologies affect tight junction permeability e.g. Crohn’s disease tight junctions more permeable

29
Q

gap junction structure/ example

A

Hexamers of conexin subunit connected end to end

Used for synchronized electrical conductance in brain and cardiac muscle.