55 research outputs found
Quantitative Performance Bounds in Biomolecular Circuits due to Temperature Uncertainty
Performance of biomolecular circuits is affected by changes in temperature, due to its influence on underlying reaction rate parameters. While these performance variations have been estimated using Monte Carlo simulations, how to analytically bound them is generally unclear. To address this, we apply control-theoretic representations of uncertainty to examples of different biomolecular circuits, developing a framework to represent uncertainty due to temperature. We estimate bounds on the steady-state performance of these circuits due to temperature uncertainty. Through an analysis of the linearised dynamics, we represent this uncertainty as a feedback uncertainty and bound the variation in the magnitude of the input-output transfer function, providing a estimate of the variation in frequency-domain properties. Finally, we bound the variation in the time trajectories, providing an estimate of variation in time-domain properties. These results should enable a framework for analytical characterisation of uncertainty in biomolecular circuit performance due to temperature variation and may help in estimating relative performance of different controllers
Period-Amplitude Co-variation in Biomolecular Oscillators
The period and amplitude of biomolecular oscillators are functionally
important properties in multiple contexts. For a biomolecular oscillator, the
overall constraints in how tuning of amplitude affects period, and vice versa,
are generally unclear. Here we investigate this co-variation of the period and
amplitude in mathematical models of biomolecular oscillators using both
simulations and analytical approximations. We computed the amplitude-period
co-variation of eleven benchmark biomolecular oscillators as their parameters
were individually varied around a nominal value, classifying the various
co-variation patterns such as a simultaneous increase/ decrease in period and
amplitude. Next, we repeated the classification using a power norm-based
amplitude metric, to account for the amplitudes of the many biomolecular
species that may be part of the oscillations, finding largely similar trends.
Finally, we calculate "scaling laws" of period-amplitude co-variation for a
subset of these benchmark oscillators finding that as the approximated period
increases, the upper bound of the amplitude increases, or reaches a constant
value. Based on these results, we discuss the effect of different parameters on
the type of period-amplitude co-variation as well as the difficulty in
achieving an oscillation with large amplitude and small period
Dynamical Consequences of Bandpass Feedback Loops in a Bacterial Phosphorelay
Under conditions of nutrient limitation, Bacillus subtilis cells terminally differentiate into a dormant spore state. Progression to sporulation is controlled by a genetic circuit consisting of a phosphorelay embedded in multiple transcriptional feedback loops, which is used to activate the master regulator Spo0A by phosphorylation. These transcriptional regulatory interactions are “bandpass”-like, in the sense that activation occurs within a limited band of Spo0A~P concentrations. Additionally, recent results show that the phosphorelay activation occurs in pulses, in a cell-cycle dependent fashion. However, the impact of these pulsed bandpass interactions on the circuit dynamics preceding sporulation remains unclear. In order to address this question, we measured key features of the bandpass interactions at the single-cell level and analyzed them in the context of a simple mathematical model. The model predicted the emergence of a delayed phase shift between the pulsing activity of the different sporulation genes, as well as the existence of a stable state, with elevated Spo0A activity but no sporulation, embedded within the dynamical structure of the system. To test the model, we used time-lapse fluorescence microscopy to measure dynamics of single cells initiating sporulation. We observed the delayed phase shift emerging during the progression to sporulation, while a re-engineering of the sporulation circuit revealed behavior resembling the predicted additional state. These results show that periodically-driven bandpass feedback loops can give rise to complex dynamics in the progression towards sporulation
A Kalman Filter Approach for Biomolecular Systems with Noise Covariance Updating
An important part of system modeling is determining parameter values,
particularly for biomolecular systems, where direct measurements of individual
parameters are typically hard. While Extended Kalman Filters have been used for
this purpose, the choice of the process noise covariance is generally unclear.
In this chapter, we address this issue for biomolecular systems using a
combination of Monte Carlo simulations and experimental data, exploiting the
dependence of the process noise covariance on the states and parameters, as
given in the Langevin framework. We adapt a Hybrid Extended Kalman Filtering
technique by updating the process noise covariance at each time step based on
estimates. We compare the performance of this framework with different fixed
values of process noise covariance in biomolecular system models, including an
oscillator model, as well as in experimentally measured data for a negative
transcriptional feedback circuit. We find that the Extended Kalman Filter with
such process noise covariance update is closer to the optimality condition in
the sense that the innovation sequence becomes white and in achieving a balance
between the mean square estimation error and parameter convergence time. The
results of this chapter may help in the use of Extended Kalman Filters for
systems where process noise covariance depends on states and/or parameters.Comment: 23 pages, 9 figure
Negative Feedback Facilitates Temperature Robustness in Biomolecular Circuit Dynamics
Temporal dynamics in many biomolecular circuits can change with temperature because
of the temperature dependence of underlying reaction rate parameters. It is generally unclear what
circuit mechanisms can inherently facilitate robustness in the dynamics to variations in temperature.
Here, we address this issue using a combination of mathematical models and experimental measurements
in a cell-free transcription-translation system. We find that negative transcriptional feedback
can reduce the effect of temperature variation on circuit dynamics. Further, we find that effective
negative feedback due to first-order degradation mechanisms can also enable such a temperature
robustness effect. Finally, we estimate temperature dependence of key parameters mediating such
negative feedback mechanisms. These results should be useful in the design of temperature robust
circuit dynamics
Quantitative Performance Bounds in Biomolecular Circuits due to Temperature Uncertainty
Performance of biomolecular circuits is affected by changes in temperature, due to its influence on underlying reaction rate parameters. While these performance variations have been estimated using Monte Carlo simulations, how to analytically bound them is generally unclear. To address this, we apply control-theoretic representations of uncertainty to examples of different biomolecular circuits, developing a framework to represent uncertainty due to temperature. We estimate bounds on the steady-state performance of these circuits due to temperature uncertainty. Through an analysis of the linearised dynamics, we represent this uncertainty as a feedback uncertainty and bound the variation in the magnitude of the input-output transfer function, providing a estimate of the variation in frequency-domain properties. Finally, we bound the variation in the time trajectories, providing an estimate of variation in time-domain properties. These results should enable a framework for analytical characterisation of uncertainty in biomolecular circuit performance due to temperature variation and may help in estimating relative performance of different controllers
Synchronization Conditions for Nonlinear Oscillator Networks
Understanding conditions for the synchronization of a network of
interconnected oscillators is a challenging problem. Typically, only sufficient
conditions are reported for the synchronization problem. Here, we adopted the
Lyapunov-Floquet theory and the Master Stability Function approach in order to
derive the synchronization conditions for a set of coupled nonlinear
oscillators. We found that the positivity of the coupling constant is a
necessary and sufficient condition for synchronizing linearly full-state
coupled identical oscillators. Moreover, in the case of partial state coupling,
the asymptotic convergence of volume in state space is ensured by a positive
coupling constant. The numerical calculation of the Master Stability Function
for a benchmark two-dimensional oscillator validates the synchronization
corresponding to the positive coupling. The results are illustrated using
numerical simulations and experimentation on benchmark oscillators.Comment: 6 pages, 7 figures, Journa
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