SLIDING FILAMENT THEORY What are Cross-bridges? •       With an electron microscope, fine cross bridges can be seen...

SLIDING FILAMENT THEORY |FINDYOURSELF

July 19, 2019 2 Comments




SLIDING FILAMENT THEORY






What are Cross-bridges?
      With an electron microscope, fine cross bridges can be seen extending from each thick filament to the thin filament. These are formed by the arm and head of the myosin molecules projecting outward from the tail, and pointing towards the thin filaments.

SLIDING FILAMENT THEORY

Definition:
When a muscle cell contracts, the thin filaments slide past the thick filaments, and the sarcomere shortens. This process comprised of several steps is called the Sliding Filament Theory. It is also called the Walk Along Theory or the Ratchet Theory. 

After the ATP has bound to the myosin head, the binding of Myosin to Actin molecule takes place:
Once the actin active sites are uncovered, the myosin binds to it:

It has the following steps:
1.                      Before contraction begins, An ATP molecule binds to the myosin head of the cross-bridges.
2.                      The ATPase activity of the myosin head immediately cleaves the ATP molecule but the products (ADP+P) remains bound to the head. Now the myosin head is in a high energy state and ready to bind to the actin molecule.
3.                      When the troponin-tropomyosin complex binds with calcium ions that come from the sarcoplasmic reticulum, it pulls the tropomyosin so that the active sites on the actin filaments for the attachment of the myosin molecule are uncovered.
4.                      Myosin head binds to the active site on the actin molecule.
5.                      The bond b/w the head of the cross bridges(myosin) & the actin filaments causes a the bridge to change shape bending 45° inwards as if it was on a hinge, stroking towards the centre of the sarcomere, like the stroking of a boat oar. This is called a POWER STROKE.
6.                      This power stroke pulls the thin filament inward only a small distance.
7.                      Once the head tilts, this allows release of ADP & phosphate ions.
8.                      At the site of release of ADP, a new ATP binds. This binding causes the detachment of the myosin head from the actin.
9.                      A new cycle of attachment-detachment-attachment begins.
10.             Repeated cycles of cross-bridge binding, bending and detachment complete the shortening and contraction of the muscle.
11.             Participant                Will bind to:
1. Myosin                        ATP, Actin
2. Actin                      Myosin, Troponin
3. Tropomyosin          Troponin
4. Troponin                Calcium, Actin ,                                             Tropomyosin
5. ATP                        Myosin
6. Calcium ions          Troponin




      Through the attachment-detachment-attachment cycle, the myosin heads or cross bridges “walk” along an actin filament to pull it inward relative to the stationary thick filament.
       Because of the way the myosin molecules are oriented within a thick filament, all the cross-bridges stroke towards the center of the sarcomere.
      At any time during contraction, part of the cross bridges are attached to the thin filaments and are stroking, while others are returning to their original conformation in preparation for binding with another actin molecule. Thus, some cross-bridges “hold on” while others “let go”. Otherwise, the thin filaments would slip back to their resting position b/w strokes.
      The detachment of the myosin head from the actin cannot take place until and unless a new ATP does not attach to the myosin head. This is important when death occurs, no more ATP is available and thus, rigor mortis occurs. 
Shortening of the Muscle:
    The thick and thin filaments DO NOT shorten.
    Contraction is accomplished by the thin filaments from opposite sides of each sarcomere sliding closer together or overlapping the thick filaments further.
    The H-zone becomes smaller as the thin filaments approach each other.
    The I band becomes smaller as the thin filaments further overlap the thick filaments.
    The width of the A band remains unchanged as it depends on the thick filaments and the thick filaments do not change length.