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Baetica, A.-A.

Publications and source records attributed to Baetica, A.-A..

5 recordsLinked to original sources

Context Dependence of Biological Circuits

It has been an ongoing scientific debate whether biological parameters are conserved across experimental setups with different media, pH values, and other experimental conditions. Our work explores this question using Bayesian probability as a rigorous framework to assess the biological context of parameters in a model of the cell growth controller in You et al. When this growth controller is uninduced, the E. coli cell population grows to carrying capacity; however, when the circuit is induced, the cell population growth is regulated to remain well below carrying capacity. This growth control controller regulates the E. coli cell population by cell-cell communication using the signaling molecule AHL and by cell death using the bacterial toxin CcdB.\n\nTo evaluate the context dependence of parameters such as the cell growth rate, the carrying capacity, the AHL degradation rate, the leakiness of AHL, the leakiness of toxin CcdB, and the IPTG induction factor, we collect experimental data from the growth control circuit in two different media, at two different pH values, and with several induction levels. We define a set of possible context-dependencies that describe how these parameters may differ with the experimental conditions and we develop mathematical models of the growth controller across the different experimental contexts. We then determine whether these parameters are shared across experimental contexts or whether they are context-dependent. For each of these possible context-dependencies, we use Bayesian inference to assess its plausibility and to estimate the growth controllers parameters assuming this context-dependency. Ultimately, we find that there is significant experimental context-dependence in this circuit. Moreover, we also find that the estimated parameter values are sensitive to our assumption of a context relationship.

synthetic biology

Hard Limits And Performance Tradeoffs In A Class Of Sequestration Feedback Systems

Feedback regulation is pervasive in biology at both the organismal and cellular level. In this article, we explore the properties of a particular biomolecular feedback mechanism implemented using the sequestration binding of two molecules. Our work develops an analytic framework for understanding the hard limits, performance tradeoffs, and architectural properties of this simple model of biological feedback control. Using tools from control theory, we show that there are simple parametric relationships that determine both the stability and the performance of these systems in terms of speed, robustness, steady-state error, and leakiness. These findings yield a holistic understanding of the behavior of sequestration feedback and contribute to a more general theory of biological control systems.

systems biology

Population regulation in microbial consortia using dual feedback control

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.

synthetic biology

Finding analytic stationary solutions to the chemical master equation by gluing state spaces at one or two states recursively

Noise is often indispensable to key cellular activities, such as gene expression, necessitating the use of stochastic models to capture its dynamics. The chemical master equation (CME) is a commonly used stochastic model that describes how the probability distribution of a chemically reacting system varies with time. Knowing analytic solutions to the CME can have benefits, such as expediting simulations of multiscale biochemical reaction networks and aiding the design of distributional responses. However, analytic solutions are rarely known. A recent method of computing analytic stationary solutions relies on gluing simple state spaces together recursively at one or two states. We explore the capabilities of this method and introduce algorithms to derive analytic stationary solutions to the CME. We first formally characterise state spaces that can be constructed by performing single-state gluing of paths, cycles or both sequentially. We then study stochastic biochemical reaction networks that consist of reversible, elementary reactions with two-dimensional state spaces. We also discuss extending the method to infinite state spaces and designing stationary distributions that satisfy user-specified constraints. Finally, we illustrate the aforementioned ideas using examples that include two interconnected transcriptional components and chemical reactions with two-dimensional state spaces.\n\nSubject AreasSystems biology, synthetic biology, biomathematics, bioengineering

systems biology

A Bayesian approach to inferring chemical signal timing and amplitude in a temporal logic gate using the cell population distributional response

1. Introduction 1. Introduction 2. The temporal logic... 3. Bayesian event detection... 4. Applying the Bayesian... 5. Conclusion References Stochastic gene expression poses an important challenge for engineering robust behaviors in a heterogeneous cell population [1]. Cells address this challenge using the distribution of cellular responses during some gene regulation and differentiation processes [2]. Similarly, the temporal logic gate design in Hsiao et al. [3] considers the distribution of responses across a cell population. The design employs integrases Bxb1 and TP901-1 [4] to engineer an E. coli strain with four DNA states that record the temporal order of two chemical signals. Hsiao et al. [3] also use the heter ...

synthetic biology