Sliding Filament Theory (Muscle Contraction) Flashcards
Explains how actin and myosin filaments interact during skeletal muscle contraction.
During skeletal muscle contraction, actin (thin) and myosin (thick) filaments interact via a “sliding filament” mechanism, where myosin heads, powered by ATP, bind to actin, pull it inward, and then detach, repeating this cycle to shorten the muscle fiber
1st Steps in Muscle Contraction
- Excitation: An action potential reaches the neuromuscular junction.
- Acetylcholine (ACh) is released from the presynaptic terminal.
- ACh binds to nicotinic receptors on the sarcolemma (muscle membrane).
- This triggers depolarization, initiating an action potential that propagates along the sarcolemma and down the T-tubules.
2nd Steps in Muscle Contraction
Calcium Release: The action potential activates voltage-sensitive dihydropyridine receptors (DHPR) on T-tubules, mechanically linked to ryanodine receptors (RyR) on the sarcoplasmic reticulum (SR).
* This causes calcium ions (Ca²⁺) to be released from the SR into the sarcoplasm.
3rd Steps in Muscle Contraction
Cross-Bridge Formation:
Ca²⁺ binds to troponin C, a component of the troponin complex on the actin filament.
* This induces a conformational change that shifts tropomyosin, exposing myosin-binding sites on actin.
* Energized myosin heads (with ADP + Pi bound) attach to the exposed sites on actin, forming cross-bridges.
4th Steps in Muscle Contraction
Power Stroke: ADP and Pi are released from the myosin head.
* This triggers the power stroke, where the myosin head pivots, pulling the actin filament toward the center of the sarcomere (M-line).
* ATP binds to the myosin head, causing it to detach from actin.
5th Steps in Muscle Contraction
Relaxation: Ca²⁺ is actively pumped back into the SR by SERCA (sarcoplasmic/endoplasmic reticulum Ca²⁺ ATPase) pumps.
* The drop in Ca²⁺ levels leads to tropomyosin covering the myosin-binding sites on actin.
* Without cross-bridge cycling, the muscle relaxes and returns to its resting length.
Role of ATP in Muscle Contraction
Required to detach myosin from actin after the power stroke.
* Hydrolysis of ATP re-cocks the myosin head for another cycle.
* Powers calcium reuptake into the SR via SERCA pumps during relaxation.
Muscular Dystrophy:
A group of genetic disorders, including Duchenne Muscular Dystrophy, caused by mutations in the dystrophin gene.
* Dystrophin stabilizes the sarcolemma during contraction.
* Lack of dystrophin leads to muscle fibre damage, weakness, and progressive wasting due to impaired transmission of force and calcium handling.