The statistical mechanics of cross-bridge action is considered in order to develop constitutive equations that express fiber tension as a function of degree of activation and time history of speed of contraction. The kinetic equation of A.F. Huxley (1) is generalized to apply to the partially activated state. The rate parameters of attachment and detachment, and cross-bridge compliance are assumed to be step functions of extension, x, with a finite number of discontinuities. This assumption enables integration of the kinetic equation and its moments with respect to x resulting in analytic equations from which x has been eliminated. When the constants in the rate parameters and the force function are chosen so that Hill's force-velocity rela...
Force development in smooth muscle, as in skeletal muscle, is believed to reflect recruitment of for...
We describe a model that relates the maximum shortening velocity of a muscle fiber, Vm, to the kinet...
AbstractThe cross-bridge stiffness can be used to estimate the number of S1 that are bound to actin ...
The statistical mechanics of cross-bridge action is considered in order to develop constitutive equa...
We have developed a model for the equilibrium attachment and detachment of myosin cross-bridges to a...
AbstractWe examined whether cross-bridge cycle models with one or two tension-generating steps can a...
A model was developed which can simulate both the transient and steady-state mechanical behavior of ...
AbstractThe presence of compliance in the lattice of filaments in muscle raises a number of concerns...
Whereas the mechanical behavior of fully activated fibers can be explained by assuming that attached...
A model has been developed for characterizing the interaction between strongly-binding myosin cross-...
A simple model of a double-headed crossbridge is introduced to explain the retardation of force deca...
The responses of muscle to steady and stepwise shortening are simulated with a model in which actin-...
Force and length steps, applied to a muscle fiber in the isometric state, are believed to synchroni...
AbstractForce and displacement events from a single myosin molecule interacting with an actin filame...
We recently presented, in a qualitative manner, a cross-bridge model of muscle contraction which was...
Force development in smooth muscle, as in skeletal muscle, is believed to reflect recruitment of for...
We describe a model that relates the maximum shortening velocity of a muscle fiber, Vm, to the kinet...
AbstractThe cross-bridge stiffness can be used to estimate the number of S1 that are bound to actin ...
The statistical mechanics of cross-bridge action is considered in order to develop constitutive equa...
We have developed a model for the equilibrium attachment and detachment of myosin cross-bridges to a...
AbstractWe examined whether cross-bridge cycle models with one or two tension-generating steps can a...
A model was developed which can simulate both the transient and steady-state mechanical behavior of ...
AbstractThe presence of compliance in the lattice of filaments in muscle raises a number of concerns...
Whereas the mechanical behavior of fully activated fibers can be explained by assuming that attached...
A model has been developed for characterizing the interaction between strongly-binding myosin cross-...
A simple model of a double-headed crossbridge is introduced to explain the retardation of force deca...
The responses of muscle to steady and stepwise shortening are simulated with a model in which actin-...
Force and length steps, applied to a muscle fiber in the isometric state, are believed to synchroni...
AbstractForce and displacement events from a single myosin molecule interacting with an actin filame...
We recently presented, in a qualitative manner, a cross-bridge model of muscle contraction which was...
Force development in smooth muscle, as in skeletal muscle, is believed to reflect recruitment of for...
We describe a model that relates the maximum shortening velocity of a muscle fiber, Vm, to the kinet...
AbstractThe cross-bridge stiffness can be used to estimate the number of S1 that are bound to actin ...