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18.8: The Microcontraction Cycle Resolves the Contraction Paradox

  • Page ID
    89026
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    The microcontraction cycle resolves the contraction paradox:

    • ATP is necessary for muscle contraction: In step e in the illustration above, as ATP on myosin heads is hydrolyzed, the heads change from a low energy to a high-energy conformation. The myosin heads can now bind to actin monomers (step b in the microcontraction cycle). This results in the power stroke (step c). Free energy that is released by an allosteric change in myosin will pull the actin along the myosin, in effect causing a micro-shortening of the sarcomere—in other words, a contraction!
    • ATP is necessary for muscle relaxation: At the end of step c, myosin remains bound to actin until ATP can again bind to the myosin head. Binding of ATP in step d displaces ADP and inorganic phosphate (Pi)…and breaks actin-myosin crossbridges. A removal of \(\rm Ca^{++}\) from sarcomeres at the end of a contraction event blocks myosin-binding sites on actin, while the rapid breakage of actin-myosin crossbridges by ATP-myosin binding allows muscle relaxation and the sliding apart of the actin and myosin filaments (i.e., stretching). This leaves the myosin heads in the “cocked” (high-energy) conformation, ready for the next round of contraction.

    No more paradox! The displacement of ADP and Pi by ATP binding to myosin heads breaks actin-myosin crossbridges, allowing for relaxation (stretching) of the sarcomeres, and hence muscles. The hydrolysis of the ATP bound to myosin cocks the myosin head in a high free-conformation that is released during the microcontraction power stroke.

    Electron-microscopic examination of myosin-monomer heads at different ionic strengths provides visual evidence that myosin heads are flexible and can take on alternate stable conformations, as would be expected during the microcontraction cycle (Figure 18.23).

    Screen Shot 2022-05-25 at 7.41.53 PM.png
    Figure 18.23: The ability of flexible myosin heads to bend and to change conformation is consistent with their proposed activity during the microcontraction cycle.

    The arrows point to myosin heads in different conformations. This visualization was made possible by treating the preparations with antimyosin antibodies (immunoglobulins). See a cool video of conformational change in myosin monomers at Myosin Heads in Action.

    335-2 Actin-Myosin Contraction Cycle Resolves the Contraction Paradox

    336-2 ATP Binding & Hydrolysis Changes Myosin-Head Conformation


    This page titled 18.8: The Microcontraction Cycle Resolves the Contraction Paradox is shared under a not declared license and was authored, remixed, and/or curated by Gerald Bergtrom.