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Membrane waves driven by actin and Myosin.

R Shlomovitz1, N S Gov

  • 1Department of Chemical Physics, The Weizmann Institute of Science, P.O. Box 26, Rehovot, Israel 76100.

Physical Review Letters
|May 16, 2007
PubMed
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We developed a model linking membrane dynamics to actin polymerization and myosin motor forces. This model predicts robust membrane waves driven by myosin activity, consistent with cellular observations.

Area of Science:

  • Biophysics
  • Cell Biology
  • Computational Biology

Background:

  • Cellular membranes undergo dynamic shape changes driven by internal forces.
  • Actin polymerization and myosin motor activity are key regulators of cell mechanics and morphology.

Purpose of the Study:

  • To model the interplay between membrane properties, actin polymerization, and myosin contractility.
  • To investigate the emergence of membrane dynamics, specifically transverse waves, from these coupled forces.

Main Methods:

  • Developed a theoretical model coupling membrane mechanics with protrusive (actin polymerization) and contractile (myosin motors) forces.
  • Incorporated freely diffusing membrane proteins with spontaneous curvature to activate actin polymerization.
  • Modeled myosin motor recruitment from a constant reservoir and their contractile force generation.

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  • Analyzed the system in the linear limit for all forces and variables.
  • Main Results:

    • Demonstrated that convex membrane proteins, when coupled with myosin activity, generate robust transverse membrane waves.
    • The model successfully reproduces wave-like membrane deformations similar to those observed experimentally in various cell types.
    • Showcased the critical role of myosin activity in driving these emergent wave phenomena.

    Conclusions:

    • The presented model provides a mechanistic explanation for transverse membrane wave formation.
    • Highlights the significance of coupled actin-myosin dynamics and membrane protein curvature in cellular mechanics.
    • Offers a framework for understanding force generation and membrane remodeling in biological systems.