• Title of article

    A multisegmental cross-bridge kinetics model of the myofibril

  • Author/Authors

    Stoecker، نويسنده , , Urs and Telley، نويسنده , , Ivo A. and Stüssi، نويسنده , , Edgar and Denoth، نويسنده , , Jachen، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2009
  • Pages
    13
  • From page
    714
  • To page
    726
  • Abstract
    Striated muscle is a mechanical system that develops force and generates power in serving vital activities in the body. Striated muscle is a complex biological system; a single mammalian muscle fibre contains up to hundred or even more myofibrils in parallel connected via an inter-myofibril filament network. In one single myofibril thousands of sarcomeres are lined up as a series of linear motors. We recently demonstrated that half-sarcomeres (hS) in a single myofibril operate non-uniformly. We outline a mathematical framework based on cross-bridge kinetics for the simulation of the force response and length change of individual hS in a myofibril. The model describes the muscle myofibril in contraction experiments under various conditions. The myofibril is modeled as a multisegmental mechanical system of hS models, which have active and viscoelastic properties. In the first approach, a two-state cross-bridge formalism relates the hS force to the chemical kinetics of ATP hydrolysis, as first described by Huxley [1957. Muscle structure and theories of contraction. Prog. Biophys. Mol. Biol. 7, 255–318]. Two possible types of biological variability are introduced and modeled. Numerical simulations of a myofibril composed of four to eight hS show a non-uniform hS length distribution and complex internal dynamics upon activation. We demonstrate that the steady-state approximation holds only in restricted time zones during activation. Simulations of myofibril contraction experiments that reproduce the classic steady-state force–length and force–velocity relationships, strictly constrained or “clamped” in either end-held isometric or isotonic contraction conditions, reveal a small but conspicuous effect of hS dynamics on force.
  • Keywords
    Actomyosin kinetics , Sarcomere dynamics , muscle modeling , Sarcomere length inhomogeneity , Skeletal muscle
  • Journal title
    Journal of Theoretical Biology
  • Serial Year
    2009
  • Journal title
    Journal of Theoretical Biology
  • Record number

    1539800