Sliding filament model
Key terms
Sliding filament model: movement of actin and myosin filaments in relation to each other to cause contraction
Sliding filament model
Contraction
Myosin filaments pull actin filaments inwards
Towards centre of sarcomere
Light band becomes narrower
Z lines move closer
Shortens sarcomere
H-zone becomes narrower
Dark band remains same width
Myosin filaments overlap actin filaments
Greater amount
Simultaneous contraction of lots of sarcomeres
Myofibrils and muscle fibres contract
Enough force to pull on a bone
Causes movement
Sarcomeres return to original length
Muscle relaxes
Structure of myosin
Globular heads which are hinged
Allows to move back and forwards
Binding site for each actin and ATP
Tails of myosin molecules aligned together
Form myosin filament
Structure of actin
Actin filaments have binding sites for myosin heads
Actin-myosin binding sites
Muscle in resting state
Actin-myosin sires blocked by tropomyosin
Heads can’t bind to actin
Filament can’t slide past each other
Muscle stimulated to contract
Myosin heads form bonds with actin filaments
Actin-myosin cross bridges
Myosin heads flex in unison
Pull actin filaments along myosin filament
Myosin detaches from actin
Head returns to original angle
Uses ATP
Myosin reattaches further along actin filament
Process occurs again
Repeated up to 100 times per second
Neuromuscular junction
Action potential arrives at neuromuscular junction
Muscle contraction triggered
Point where motor neurone and skeletal muscle fibre meet
Many neuromuscular junctions along muscle length
Ensure muscle fibres contract simultaneously
Contraction is powerful and fast
One one would mean this isn’t possible
Muscle fibres supplied by single motor neurone
Motor unit
Fibres act as single unit
Strong force needed
Large number of motor units stimulated
Small force needed
Small number stimulated
Action potential reaches neuromuscular junction
Stimulates calcium ion channels
Open
Calcium ions diffuse from synapse
Into synaptic knob
Synaptic vesicles fuse with presynaptic membrane
Acetylcholine released into synaptic cleft
Exocytosis
Diffuses across synapse
Binds to receptors
On postsynaptic membrane
Opens sodium ion channels
Results in depolarisation
Acetylcholine broken down by acetylcholinesterase
Into choline and ethanoic acid
Prevents muscle being overstimulated
Choline and ethanoic acid diffuse back into neurone
Recombined into acetylcholine
Uses energy provided by mitochondria
Sarcoplasm
Depolarisation of sarcolemma travels deep into muscle fibre
Spreads through T-tubules
Contact with sarcoplasm reticulum
Sarcoplasm reticulum contains stored calcium ions
Actively absorbs from sarcoplasm
Action potential reaches sarcoplasmic reticulum
Stimulates calcium ion channels to open
Calcium ions diffuse down concentration gradient flooding with calcium ions
Calcium ions bind to troponin
Causes it to change shape
Pulls on tropomyosin
Moves it away from actin-myosin binding sites
Binding sites exposed
Myosin head binds to actin filaments
Form actin-myosin cross-bridge
Attached to actin filament
Myosin head flexes
Pull actin filament along
Molecule of ADP bound to myosin head released
ATP molecule binds to myosin head
Head detaches from actin filament
Calcium ions present in sarcoplasm activate ATPase activity of myosin
Hydrolyses ATP to ADP and phosphate
Releases energy
Myosin head returns to original position
Myosin head attaches to another actin-myosin binding site
Further along actin filament
Cycle repeats
Cycle continues as long as muscle remains stimulated
During stimulation
Many actin-myosin bridges form and break rapidly
Pulls actin filament along
Shortens sarcomere
Muscle contracts
Energy supply during muscle contraction
Requires large quantities of energy
Provided by hydrolysis of ATP into ADP and phosphate
Energy required
Movement of myosin heads
Enable sarcoplasmic reticulum to reabsorb calcium ions from sarcoplasm
Aerobic respiration
ATP used by muscle cells
Regenerated from ADP during oxidative phosphorylation
Chemical reaction takes place inside mitochondria
Only occurs in presence of oxygen
Used for long periods of low-intensity exercise
Interaction of myosin and actin during muscle contraction
Tropomyosin molecule prevents myosin head from attaching to binding site on actin molecule
Calcium ions released from endoplasmic reticulum
Tropomyosin molecule pulls away from binding sites
Myosin head
Attaches to binding site on actin filament
Head of myosin changes angle
Moving actin filament along
ADP molecule released
ATP molecule fixes to myosin head
Detach from actin filament
Hydrolysis of ATP to ADP by myosin
Provides energy for myosin head
Resume its normal position
Head of myosin reattaches to binding site further along actin filament
Cycle repeated
Anaerobic respiration
Very active muscle
Oxygen used up more quickly than blood supply can replace it
ATP generated anaerobically
Made by glycolysis
Pyruvate produced converted into lactic acid
Builds up quickly
Results in muscle fatigue
Used for short periods of high-intensity exercise
Creatine phosphate
Stored in muscle
Acts as reserve supply of phosphate
Available immediately
Combine with ADP
Reforms ATP
Generates ATP rapidly
Store of phosphate used up quickly
Muscle relaxes
Creatine phosphate store replenished using phosphate from ATP
Used for short bursts of vigorous exercise