Highlights d Feedback control is an essential component of biomolecular systems d The design of feedback systems necessarily imposes performance tradeoffs d We use control theory to study an important class of molecular feedback motifs d Our work provides a map between biochemical parameters and circuit performance

A common feature of both biological and man-made systems is the use of feedback to control their behavior. In this paper, we explore a particular model of biomolecular feedback implemented using a sequestration mechanism. This has been demonstrated to implement robust perfect adaption, often referred to as integral control in engineering. Our work generalizes a previous model of the sequestration feedback system and develops an analytical framework for understanding the hard limits, performance tradeoffs, and architectural properties of a simple model of biological control. We find that many of the classical tools from control theory and dynamical systems can be applied to understand both deterministic and stochastic models of the system. Our work finds that there are simple expressions that determine both the stability and the performance of these systems in terms of speed, robustness, steady-state error, and noise. These findings yield a holistic picture of the general behavior of sequestration feedback, and will hopefully contribute to a more general theory of biological control systems.

Abstract-An ongoing area of study in synthetic biology has been the design and construction of synthetic circuits that maintain homeostasis at the population level. Here, we are interested in designing a synthetic control circuit that regulates the total cell population and the relative ratio between cell strains in a culture containing two different cell strains. We have developed a dual feedback control strategy that uses two separate control loops to achieve the two functions respectively. By combining both of these control loops, we have created a population regulation circuit where both the total population size and relative cell type ratio can be set by reference signals. The dynamics of the regulation circuit show robustness and adaptation to perturbations in cell growth rate and changes in cell numbers. The control architecture is general and could apply to any organism for which synthetic biology tools for quorum sensing, comparison between outputs, and growth control are available.

Many biological and physical systems exhibit population-density dependent transitions to synchronized oscillations in a process often termed “dynamical quorum sensing”. Synchronization frequently arises through chemical communication via signaling molecules distributed through an external medium. We study a simple theoretical model for dynamical quorum sensing: a heterogenous population of limit-cycle oscillators diffusively coupled through a common medium. We show that this model exhibits a rich phase diagram with four qualitatively distinct physical mechanisms that can lead to a loss of coherent population-level oscillations, including a novel mechanism arising from effective time-delays introduced by the external medium. We derive a single pair of analytic equations that allow us to calculate phase boundaries as a function of population density and show that the model reproduces many of the qualitative features of recent experiments on BZ catalytic particles as well as synthetically engineered bacteria.