Criticality and Adaptivity in Enzymatic Networks
Tuesday, November 17, 2015 - 2:30pm - 3:30pm
A major challenge for systems biology is to deduce the molecular interactions that underlie correlations observed between concentrations of different intracellular molecules. Although direct explanations such as coupled transcription or direct protein-protein interactions are often considered, potential indirect sources of coupling have received much less attention. In this work we show how strong correlations can arise generically from a post-translational coupling mechanism involving the processing of multiple protein species by a common enzyme. Using multiclass queueing theory for a stochastic model of the enzymatic network, we obtain a closed-form expression for the multi-dimensional steady-state distribution for the numbers of protein molecules which allow us to deduce moments and correlations associated with this distribution. Strikingly, correlations peak near the critical balance-point where the total input rate of proteins into the system is equal to the maximum processing capacity of the enzymes. We further extend these results to multi-component enzymatic networks and show that they also exhibit significant long-range correlations among all protein levels near the balance-point. We further show that allowing enzyme levels to adapt to protein load leads to strong correlations across a broad range of system parameters.