Myosins are a family of proteins that utilize ATP hydrolysis to move along actin filaments.
Myosin II was the first identified and isolated from skeletal muscle; previously believed to be the only type.
Today, multiple classes of myosin are known, each with diverse functions:
Movement of organelles
Muscle contraction
Cell migration
Myosins categorize as mechanochemical enzymes or motor proteins.
Composition:
Heavy chains (1-2) and several light chains.
Regions:
Head: Actin binding and nucleotide binding sites (ATP).
Neck: Contains α-helical regions, associates with light chains that regulate head activity.
Tail: Binding sites that define myosin specificity.
Consists of:
Head and Neck Domain: Includes actin-binding site.
Nucleotide-binding site.
Light chains: Essential and regulatory types.
Class I: 10-14 nm step size, functions in membrane association, endocytosis.
Class II: 5-10 nm step size, primarily involved in contraction.
Class V: 36 nm step size, movement of organelles.
In the absence of ATP, the myosin head is firmly attached to the actin (rigor mortis).
Binding ATP: Myosin head releases from actin.
Hydrolysis of ATP: Converts ATP to ADP + Pi, inducing a rotation and storing energy in a "cocked state".
Binding to Actin: Myosin in cocked state attaches to actin.
Power Stroke: Release of Pi couples with elastic energy release, moving the actin filament.
Myosin remains bound as ADP is released, awaiting ATP rebinding.
Skeletal Muscles: Composed of muscle fibers with bundles of multinucleated cells.
Each fiber contains myofibrils made up of sarcomeres:
Z Disk: Located at each end of a sarcomere, shared with adjacent sarcomeres.
I Bands: Actin thin filaments anchored to Z disk, not overlapped with myosin.
A Band: Thick filaments interdigitate with thin filaments.
Relaxed Sarcomere: Low Ca2+ concentration.
Contraction: Increased Ca2+ stimulates ATP-dependent contraction, shortening the sarcomere length by pulling actin filaments toward the center.
Tropomyosin (TM): Coiled-coil dimer covering actin, blocking myosin binding in low Ca2+
Troponin: Complex that regulates TM position via Ca2+ binding.
Low Ca2+: TM prevents cross-bridge cycling.
High Ca2+: TM exposes myosin-binding sites on actin, allowing contraction.
Mutations in TN or TM can lead to cardiomyopathies.
14 distinct families; humans have 45.
N-terminal microtubule binding domain and coiled coil linker
Move processively using ATP, mainly transporting cargo to + end.
Move towards the minus end of microtubules.
Composed of heavy chains (1-3) that contain the motor domain, and intermediate and light chains, a very large protein complex (1.5 megaDaltons)
1) Cytoplasmic, directs organelle movement and positions centrosome and nucleus during cell migration, aids construction of microtubular spindle
2) Axonemal Dyneins – required for beating of cilia and flagella
Contains multiple subunits, ATP hydrolysis facilitates movement.
Stalk contains the MT binding head
ATP bound the stalk is detached from MT
ATP hydrolysis causes attachment to MT
Release of ADP + Pi cause powerstroke and movement of MT by 8nm
Dynactin Complex:
Assists cytoplasmic dynein in cargo transport; binds to dynein and cargo, regulated by protein interactions.
The protein BicD connects dynein and dynactin
BicD then interacts with other proteins bound to cargo allowing the complex to identify and move a range of cargos
Kinesin transports cargo to the + end; dynein to the - end.
Various cargoes include organelles like lysosomes, mitochondria, Golgi, etc.
Types of motors: Myosin V, Kinesin 1, Dynein.
Functions supported by cargo-binding tail domains and motor head domains.