The process of muscular contraction occurs over a number of key steps, including:
Depolarisation and calcium ion release
Actin and myosin cross-bridge formation
Sliding mechanism of actin and myosin filaments
Sarcomere shortening (muscle contraction)
1. Calcium Ion Release
Contraction of a muscle fibre begins when an action potential from a motor neuron triggers the release of acetylcholine into the neuromuscular junction (motor end plate)
Acetylcholine initiates depolarisation within the sarcolemma, which is spread through the muscle fibre via membrane invaginations called T tubules
Depolarisation causes the sarcoplasmic reticulum to release stores of calcium ions, which play a pivotal role in initiating muscular contractions
2. Cross-Bridge Formation
Muscle fibres contain long myofibrils composed of a protein complex of actin and myosin (myofilaments)
On actin, the binding sites for the myosin heads are covered by a blocking complex (troponin and tropomyosin)
Calcium ions bind to troponin and reconfigure the complex, exposing the binding sites that were being blocked by tropomyosin
With the binding sites now exposed, the myosin heads form a cross-bridge with the actin filaments
3. Sliding Mechanism
ATP binds to the myosin head, breaking the cross-bridge between actin and myosin
ATP hydrolysis causes the myosin heads to change position and swivel, moving them towards the next actin binding site
The myosin heads bind to the new actin sites and return to their original conformation
This reorientation drags the actin along the myosin in a sliding mechanism
4. Sarcomere Shortening
The myofilaments form structural units called sarcomeres (each sarcomere functions as a contractile unit)
Actin filaments are attached directly to Z lines, while myosin filaments are anchored to Z lines via the protein titin
As actin filaments slide along the myosin, the actin pulls the Z lines closer together, shortening the sarcomere
As the individual sarcomeres become shorter in length, the muscle fibres as a whole contracts
Muscle relaxation relies on a protein called titin, which connects the myosin filaments to the Z line
The many folds of the titin molecule gives it spring-like properties, allowing it to store elastic potential energy
Titin can either be compressed (during muscle contraction) or stretched (during muscle relaxation)
The titin can then recoil and convert its elastic potential energy into kinetic energy, moving Z lines apart (if compressed) or closer together (if stretched)
The stretching of a muscle requires a second muscle, as muscles can only work by contracting
Hence, skeletal muscles work in antagonistic pairs – when one muscle contracts, the other muscle relaxes
When titin is compressed in one muscle, it will lengthen in the antagonistic muscle (gaining elastic potential energy in both)