Lattice-gas model for active vesicle transport by molecular motors with opposite polarities

TL;DR

This paper presents a multi-species lattice gas model based on TASEP to analyze collective vesicle transport by molecular motors with opposite polarities, revealing complex phase behaviors and flux reversal mechanisms.

Contribution

It introduces a novel multi-species lattice gas model incorporating interconversion and boundary processes to study bidirectional vesicle transport.

Findings

Identification of regimes with three-phase coexistence

Discovery of phase re-entrance phenomena

Demonstration of flux reversal and polarization in vesicle distributions

Abstract

We introduce a multi-species lattice gas model for motor protein driven collective cargo transport on cellular filaments. We use this model to describe and analyze the collective motion of interacting vesicle cargoes being carried by oppositely directed molecular motors, moving on a single biofilament. Building on a totally asymmetric exclusion process (TASEP) to characterize the motion of the interacting cargoes, we allow for mass exchange with the environment, input and output at filament boundaries and focus on the role of interconversion rates and how they affect the directionality of the net cargo transport. We quantify the effect of the various different competing processes in terms of non-equilibrium phase diagrams. The interplay of interconversion rates, which allow for flux reversal and evaporation/deposition processes introduce qualitatively new features in the phase diagrams. We observe regimes of three-phase coexistence, the possibility of phase re-entrance and a significant flexibility in how the different phase boundaries shift in response to changes in control parameters. The moving steady state solutions of this model allows for different possibilities for the spatial distribution of cargo vesicles, ranging from homogeneous distribution of vesicles to polarized distributions, characterized by inhomogeneities or {\it shocks}. Current reversals due to internal regulation emerge naturally within the framework of this model. We believe this minimal model will clarify the understanding of many features of collective vesicle transport, apart from serving as the basis for building more exact quantitative models for vesicle transport relevant to various {\it in-vivo} situations.