Abstract

Cellular receptors on the cell membrane can bind ligand molecules in the extra-cellular medium to form ligand-bound monomers. These interactions ultimately determine the fate of a cell through the resulting intra-cellular signalling cascades. Often, several receptor types can bind a shared ligand leading to the formation of different monomeric complexes, and in turn to competition for the common ligand. Here, we describe competition between two receptors which bind a common ligand in terms of a bi-variate stochastic process. The stochastic description is important to account for fluctuations in the number of molecules. Our interest is in computing two summary statistics—the steady-state distribution of the number of bound monomers and the time to reach a threshold number of monomers of a given kind. The matrix-analytic approach developed in this manuscript is exact, but becomes impractical as the number of molecules in the system increases. Thus, we present novel approximations which can work under low-to-moderate competition scenarios. Our results apply to systems with a larger number of population species (i.e., receptors) competing for a common resource (i.e., ligands), and to competition systems outside the area of molecular dynamics, such as Mathematical Ecology.

Highlights

  • Receptors play a significant role in determining the fate of cells through the initiation of intra-cellular phosphorylation cascades [1,2,3,4,5]

  • We explore the timescales for monomer formation where bound monomers are only considered to be productive if they remain bound for longer than a given dwell time, τ

  • Along with the exact analysis, and for scenarios where the large number of molecules leads to a huge number of states in SX, in turn making the Exact Matrix-Analytic Approach (EMA) computationally intractable, we propose novel approximations to compute the proposed summary statistics

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Summary

Introduction

Receptors play a significant role in determining the fate of cells through the initiation of intra-cellular phosphorylation (signalling) cascades [1,2,3,4,5]. For receptors on the cellular membrane, these cascades can be initiated by the binding of a ligand molecule, in the extra-cellular medium, to the extra-cellular domain of the receptor, forming a monomer. The fate of the cell, for example division, death or migration, will be determined by the specific receptor-ligand interaction and by the number of phosphorylated monomers. Ligand molecules are capable of binding to more than one kind of receptor [4,6] These receptors may be similar in structure, yet different receptor-ligand interactions might lead to strikingly diverse cellular outcomes [7]. It is important to quantify the number, and timescales of formation, of the different ligand-bound monomers on the cell membrane

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