Team:BCCS-Bristol/Modeling-GRN

Gene Regulatory Networks (GRN) Modelling

Introduction

Sender

The sender device consists of two genes (LuxI, GFP) and a single promoter (pCpxR). We are interested in the relationship between the activator protein CpxR and the production of the signalling compound N-acyl-homoserine lactone (AHL). AHL is produced by the LuxI enzyme which uses S-adenosylmethionine and the acylated-acyl carrier protein as substrates for the reaction. The concentration of the activator protein CpxR is specified as a contact profile mimicking the discovery of a particle. A linear piece-wise function was selected, ranging from 0 at t = 0, to a maximal CpxR protein concentration C_pMax after 1 hour, taken from [15]. In the following equation time t is measured in minutes,

Both LuxI and GFP are controlled by the promoter pCpxR. In reality, because both genes are under the control of a single promoter, transcription would lead to the creation of a single mRNA strand. This mRNA would contain both genes, however, have separate ribosome binding sites (RBS) for each to allow for parallel translation. Due to the negligible effect on dynamics and a lack of information regarding degradation rates of this mRNA sequence, each gene transcription was treated separately. The transcription phase was modelled using a Hill function for the activation of the promoter with a degradation term for existing mRNA. This gives the following for mRNA concentrations of LuxI I_m and GFP G_m:

Translation of the mRNAs into proteins of LuxI I_p and GFP G_p was modelled as proportional to the current mRNA concentrations minus a degradation term, yielding the model:

Transport

Reciever