LEC37: Cytoskeleton Flashcards

1
Q

cytoskeleton function?

A

organizes intracellular components and helps cells interact mechanically w/ the environment & promote coordinated movements of cells

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2
Q

filament types of cytoskeleton

A

intermediate filaments, microtubules, actin

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3
Q

gross structure of cytoskeleton filaments

A

monomers, protein subunits, that polymerize into filaments

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4
Q

what do eukaryotic cells have in cytoskeleton

A

actin, tubulin

metazoans have IF

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5
Q

IF function?

A

allows cells to be stretched out

have high tensile strength

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6
Q

IF structure

A

IF monomer: elongated and alpha-helical w/ globular N-terminus, globular C-terminal tail

forms a dimer that’s a coiled coil

dimers associate to form staggered tetramer

each tetramer forms associates / 7 others, forms filament of 8 tetramers

IF have NO POLARITY b/c tetramers form head to tail

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7
Q

where are IF

A

around NUCLEUS, forms a network toward cell peripher

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8
Q

what do IF interact w/

A

junction proteins- desmosomes, hemidesmosomes

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9
Q

IF families of proteins?

A

1) keratin: in epithelial cells, barrier function, hair, nails
2) desmins/vimentin: mesenchymal and muscle cells
3) neurofilaments: neurons
4) lamins: nucleus of every cell

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10
Q

mutations in keratins causes?

A

disease i.e. epidermolysis bullosa simplex, blistering of skin as a fxn of mechanical stress

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11
Q

what is keratin function?

A

family of IF

protects cells, assists in resisting stretching forces

works b/c IF in cells can stretch & not break

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12
Q

how are neurofilaments associated w/ disease?

A

NF are an IF

amytrophic lateral sclerosis, ALS, Lou Gegrigs disease, aka motor neuron disease

if NF accumulate abrnoamlly in axon and cell body or motor neurons

overexpression of NF causes similar mouse phenotype

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13
Q

do IF have reversible assembly ability?

A

only nuclear lamins do

during cell cycle, a lamin protein is phoshporylated, which is signal for disassembly; after mitosis, reassembles in the nucleus

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14
Q

result of lamins mutations?

A

Progeria: disease resulting from premature aging

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15
Q

what are microtubules function

A

long, hollow tubes; intracellular oganization and intracellular transport

form the mitotic spindle, cilia, flagella

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16
Q

where do cellular MT grow from

A

the centrosome

17
Q

structure of MT?

A

grow from a tubulin dimer of a-tubin & b-tubulin; both bind GTP

MTs form a linear protofilament, which organizes laterall into a tube containing 13 protofilaments

18
Q

do MT have polarity?

A

yes

b/c dimers prefer to bind to exposed B-tublin surface, rather than a-tubulin in a protofilament

B-tubilin: + end; a-tubulin: - end (centrosome end) which binds to structures composed of gamma-tubulin

19
Q

how does MT growth occur

A

dynamic instability

the minus end is stuck in the centrosome; the plus end grows as the beta subunit hydrolyzes GTP to GDP, causing dimer to bind to a MT and tubulin to peel away at the (+) end

20
Q

what destabilizes/stops MT growth?

A

if there is lots of tubulin dimer bound to the +, cap end of the MT this destabilizes it, GDP tubulin is released into cytosol

21
Q

what prevents MT polymerization?

A

drugs- colchicine/vinblastine

22
Q

what prevents MT depolymerization?

A

taxol, a chemotherapeutics drug

23
Q

what forms mitotic spindles?

A

MT

for chromosome separation during mitosis

24
Q

what forms axon tracks?

A

MT

can be up to a meter long

very stable trakcs, unlike dynamic MT

ensures there’s no instability on the track

25
Q

what are motor proteins of MT?

A

kinesins: plus-end directed
dyneins: minus-end directed

bind to an organelle (i.e. mitochondria), bind on the other end to the MT

26
Q

how does chromosome separation occur?

A

MT, mitotic spindle

MT connects to kientochord, dissolve there, and then rebind; thus pull spindles apart via dynamic instability, during anaphase

27
Q

what is cilia and flagella structure

A

have a 9 + 2 array of MTs inside

facilitates wavelength/beating motion

28
Q

what propagates flagella movement?

A

dynein motors, which’re bind to MT, form a sliding motion, which translates to a bend, where 1 end of motor stays in 1 plae and other end moves

smooth, processive fashion of movement from 1 dynein motor to the other

29
Q

where are cilia found?

A

used for movement of materials over cells

respiratory tract, for moving mucus

oviducts, for moving eggs

30
Q

actin function?

A

for movement - of cells by crawling, and in muscle contraction

in adherens belt

microvilli

filopodia

phagocytosis

moving endocytic vesicles

contractile ring

helps cells divide

31
Q

actin structure?

A

monomer protein, G-actin

has a + and a - end

32
Q

how does cell crawling occur?

A

actin is concentrated underneath plasma membrane, at cell cortex, in network/meshwork, which gives plasma membrane shape

actin polymerization at plus end pushes plasma membrane outward in form of sheets, lamellipodia, and spikes, filopodia

lamellipodia/filopodia attach to a solid surface, drag cell body forward due to actin/myosin contractile bundles

33
Q

what powers bacteria eg listeria movement

A

actin

powers them to move within cells, into neighboring cells

34
Q

what extracellular signals can control cell movement?

A

growth factors, via small GTPases, Rho, Rac, Cdc42

these activate formation of actin into assemblies such as stress fibers, lamellipodia, filopodia

35
Q

how does actin tradmilling occur

A

actin binds & hydrolyzes ATP which allows actin filaments to grow at plus end, shrink at minus end

36
Q

why can actin form so many different structures in cells

A

because of many actin binding proteins

allow actin monomers to form many configurations of proteins

37
Q

sarcomere structure?

A

whole unit: sarcomere

thick filament in middle: myosin

thin filament: actin

Z disc bisects actin filament

38
Q

myosin II structure, function?

A

protein that forms filaments w/ protruding head domains that bind directly to actin, stimulate sliding

this sliding on actin in sarcomere is muscle contraction

39
Q

what activates muscle contraction?

A

influx of Ca2+ from sarcoplasmic reticulum activates myosin binding to actin filaments, binding and sliding is muscle contraction