thin, flexible, give mechanical support, and can change shape of a membrane for muscle contraction
microfilament size
7nm
microfilaments change length by rapid polymemerisation and depolymerisation of actin subunits
when actin subunit is bound to ATP, it has a higher affinity for the filament, the longer it is bound the higher the likelyhood of ATP hydralising to from ADP
monomers are incorporated into filament via non covalent interactions
actin regulates microfilament dynamics (stop or facilitate polymerisation)
actin forms a track fro the myosin protein to form contractile structures
microtubules
made from tubulin, long hollow cylinders
microtubule action
form cell division spindle, transport tracks for kinesin and dynein, power flagella and cilia
microtubule size
25nm and less flexible
how do microtubules constantly change length
rapid polymerisation and depolymerisation of tubulin subunits
when a microtubule is no longer needed, it can be removed and subunits reassemble elsewhere
how is a GDP cap formed
polymer assembles quickly, meaning a new subunit will be added before hydrolisation
if something slows formation of microtubule, formation of GDP from GTP occurs more quickly and results in disassembly
MTOC action
anchors minus end of microtubules
intermediate filament
stable to provide strength and support
intermediate filament size
10nm
intermediate filament composition
fibrous proteins
myosin action
travels along microfilaments for cell movement and contraction
dynein action
travels towards negative end of microtubules for vesicle transport, also beating of flagella and cilia
kinesin action
travel towards positive end of microtubules for vesicle and organelle transport
3 motor proteins
myosin, dynein, kinesin
bundles of myosin forms muscle thick filaments
actin thin filaments slide past thick filaments to contract muscle
sacomere shortens from contraction of myosin, contracting muscle
tropomyosin action at rest
blocks access to myosin binding sites on actin
calcium action in contraction
nerve imulses release calcium, that binds to toponin, complex then exposes myosin binding sites for contraction
dynein in flagella nad cilia
dynein moves along microtubules to power movement
microfilament distribution is concentrated beneath the plasma membrane
microfilaments form:
microvilli, cytoplasmic contractile bundles, lamellipodia, filipodia, cell division contractile ring
actin molecules are joined by non-covalent bonds
microfilaments can have proteins bound to them to make them more stable
betatubulin is always exposed at the positive end
MTOC is found at the base of flagella and cilia, as well as anchoring microtubules
centrosome is the starting point for tubular formation
cycles of conformationalchange produce movement of myosinhead along actin filament