A Stochastic Multiscale Model of Cardiac Thin Filament Activation Using Brownian-Langevin Dynamics

Biophys J. 2019 Dec 17;117(12):2255-2272. doi: 10.1016/j.bpj.2019.08.003. Epub 2019 Aug 9.

Abstract

We use Brownian-Langevin dynamics principles to derive a coarse-graining multiscale myofilament model that can describe the thin-filament activation process during contraction. The model links atomistic molecular simulations of protein-protein interactions in the thin-filament regulatory unit to sarcomere-level activation dynamics. We first calculate the molecular interaction energy between tropomyosin and actin surface using Brownian dynamics simulations. This energy profile is then generalized to account for the observed tropomyosin transitions between its regulatory stable states. The generalized energy landscape then served as a basis for developing a filament-scale model using Langevin dynamics. This integrated analysis, spanning molecular to thin-filament scales, is capable of tracking the events of the tropomyosin conformational changes as it moves over the actin surface. The tropomyosin coil with flexible overlap regions between adjacent tropomyosins is represented in the model as a system of coupled stochastic ordinary differential equations. The proposed multiscale approach provides a more detailed molecular connection between tropomyosin dynamics, the trompomyosin-actin interaction-energy landscape, and the generated force by the sarcomere.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Actin Cytoskeleton / chemistry*
  • Actin Cytoskeleton / metabolism*
  • Actins / chemistry
  • Actins / metabolism
  • Biomechanical Phenomena
  • Calcium / metabolism
  • Models, Molecular*
  • Movement
  • Myocardial Contraction
  • Myocardium / metabolism*
  • Protein Conformation
  • Sarcomeres / metabolism
  • Sarcomeres / physiology
  • Stochastic Processes
  • Tropomyosin / metabolism

Substances

  • Actins
  • Tropomyosin
  • Calcium