Maximizing Information Gain for the Characterization of Biomolecular Circuits

Abstract

Quantitatively predictive models of biomolecular circuits are important tools for the design of synthetic biology and molecular communication circuits. The information content of typical time-lapse single-cell data for the inference of kinetic parameters is not only limited by measurement uncertainty and intrinsic stochasticity, but also by the employed perturbations. Novel microfluidic devices enable the synthesis of temporal chemical concentration profiles. The informativeness of a perturbation can be quantified based on mutual information. We propose an approximate method to perform optimal experimental design of such perturbation profiles. To estimate the mutual information we perform a multivariate log-normal approximation of the joint distribution over parameters and observations and scan the design space using Metropolis-Hastings sampling. The method is demonstrated by finding optimal perturbation sequences for synthetic case studies on a gene expression model with varying reporter characteristics.