Exploiting intrinsic fluctuations to identify model parameters

Parameterisation of kinetic models plays a central role in computational systems biology. Besides the lack of experimental data of high enough quality, some of the biggest challenges here are identification issues. Model parameters can be structurally non‐identifiable because of functional relationships. Noise in measured data is usually considered to be a nuisance for parameter estimation. However, it turns out that intrinsic fluctuations in particle numbers can make parameters identifiable that were previously non‐identifiable. The authors present a method to identify model parameters that are structurally non‐identifiable in a deterministic framework. The method takes time course recordings of biochemical systems in steady state or transient state as input. Often a functional relationship between parameters presents itself by a one‐dimensional manifold in parameter space containing parameter sets of optimal goodness. Although the system''s behaviour cannot be distinguished on this manifold in a deterministic framework it might be distinguishable in a stochastic modelling framework. Their method exploits this by using an objective function that includes a measure for fluctuations in particle numbers. They show on three example models, immigration‐death, gene expression and Epo‐EpoReceptor interaction, that this resolves the non‐identifiability even in the case of measurement noise with known amplitude. The method is applied to partially observed recordings of biochemical systems with measurement noise. It is simple to implement and it is usually very fast to compute. This optimisation can be realised in a classical or Bayesian fashion.Inspec keywords: biochemistry, physiological models, stochastic processes, measurement errors, fluctuations, parameter estimationOther keywords: model parameter identification, deterministic framework, biochemical system, steady state, transient state, stochastic modelling framework, objective function, immigration‐death model, gene expression, Epo–EpoReceptor interaction, stochastic fluctuations, measurement noise