The monomers of microtubules are a-tubulins and b-tubulins
The monomers of microfilaments are g-actins
Unlike microtubules and microfilaments, intermediate filaments are not polar
Functions of microtubules include support, intracellular transport, and cell organization
Motor units of microtubules are kinesins and dyneins
Motor proteins of microfilaments, specifically actin filaments, are myosins.
External stimuli are converted to signal transduction pathways that convey information to the cytoskeleton, resulting in the reorganization and movement of organelles or the change of cell shape, movement, and contraction
There are two types of microtubules: cytoplasmic and axonemal microtubules
Cytoplasmic microtubules are found in the cytosol and are responsible for
maintaining axons
formation of mitotic and meiotic spindles
placement and movement of vesicles
maintaining or altering cell shape
Axonemal microtubules include the organized and stable microtubules found in structures specialized for movement such as
cilia
flagella
basal bodies to which cilia and flagella attach
Microtubules are composed of typically 13 protofilaments, whose subunits are a heterodimer of tublin, consisting of an a-tubulin and a b-tubulin, both being globular proteins
a-tubulin and b-tubulin bind non-covalently to form an ab-heterodimer
GTP in a tubulin is physically trapped at the dimer interface and is never hydrolyzed or exchanged
The GTP in the b tubulin can be hydrolyzed, exchanged, and converted to GDP
All the dimers in microtubules are oriented in the same way, resulting in protofilaments having polarized minus ends and plus ends
Microtubules resist forces that might compress or bend the fiber for mechanical support
Nocodazole or colchicine promotes microtubule assembly, resulting in the dispersal of golgi elements into separate golgi stacks scattered throughout the cytoplasm
Kinesin is an anterograde motor, heading towards the plus end of the microtubule.
Dynein is a retrograde motor, heading towards the minus end of a microtubule
Kinesin and dynein move along microtubule tracks
Myosin moves along microfilament tracks
Molecular motors convert energy from ATP into mechanical energy
Molecular motors move unidirectionally along their cytoskeletal track in a stepwise manner
Each kinesin step is approximately 8 nm, the length of one tubulin dimer, and requires the hydrolysis of a single ATP molecule
Kinesin movement
proportional to the ATP concentration
moves in a "hand-over-hand" mechanism
is high processive
Dynamic instability: process of alternating between growing and shrinking
The dissociation rate of a GDP tubulin dimer is much more rapid than the dissociation of a GTP tubulin dimer
Nucleation of microtubules occur at microtubule-organizing centers
Microtubule-organizing centers (MTOCs) control the number of microtubules, their polarity, the number of protofilaments that make up their walls, and the time and location of their assembly
Centrioles: short cylinders of modified microtubules
Y turc: tubulin ring complex where nucleation occurs
The growth of microtubules occurs by addition of subunits at the plus end of the polymer away from the centrosome, while the minus end is anchored at the centrosome
Centrioles: short cylinders of modified microtubules
Nucleation of a microtubule begins with y-tubulin at the minus end and is initiated by the yturcs: tubulin ring complex
Y-turc: helical array of y-tubulin subunits where ab-tubulin dimers assemble
Astral microtubules: project towards the cell cortex and interact with it thereby orienting the spindle of division
Kinetochore microtubules: connected to chromosomes
Polar microtubules: interact with microtubules from the opposite pole of the cell
At prophase, the nuclear lamina (intermediate filaments) is phosphorylated and de-polymerized
At prometaphase, the plus end of the kinetochore microtubules attach to the kinetochore belonging to the centromere of a chromosome