Stochastic single-particle based simulations of cellular signaling embedded into computational models of cellular morphology

Abstract

Cells exhibit a wide variety of different shapes. This diversity poses a challenge for computational approaches that attempt to shed light on the role cell geometry plays in regulating cell physiology and behavior. The simulation platform Simmune is capable of embedding the computational representation of signaling pathways into realistic models of cellular morphology. However, Simmune's current approach to account for the cell geometry is limited to deterministic models of reaction-diffusion processes, thus providing a coarse-grained description that ignores stochastic local fluctuations. Here we present an extension of Simmune that removes these limitations by employing an alternative computational representation of cellular geometry that is smooth and grid-free. These features make it possible to incorporate a fully stochastic, spatially resolved description of the cellular biochemistry. The alternative computational representation is compatible with Simmune's current approach for specifying molecular interactions. This means that a modeler using the approach needs to create a model of cellular biochemistry and morphology only once to be able to use it for both, deterministic and stochastic simulations.

Tasks

Reproductions