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Linden-Santangeli, N.

Publications and source records attributed to Linden-Santangeli, N..

2 recordsLinked to original sources

Systems modeling and uncertainty quantification of AMP-activated protein kinase signaling

AMP-activated protein kinase (AMPK) plays a key role in restoring cellular metabolic homeostasis after energy stress. Importantly, AMPK acts as a hub of metabolic signaling, integrating multiple inputs and acting on numerous downstream targets to activate catabolic processes and inhibit anabolic ones. Despite the importance of AMPK signaling, unlike other well-studied pathways, such as MAPK/ERK or NF-{kappa}B, only a handful of mechanistic models of AMPK signaling have been developed. Epistemic uncertainty in the biochemical mechanism of AMPK activity, combined with the complexity of the AMPK pathway, makes model development particularly challenging. Here, we leveraged uncertainty quantification methods and recently developed AMPK biosensors to construct a new, data-informed model of AMPK signaling. Specifically, we applied Bayesian parameter estimation and model selection to ensure that model predictions and assumptions are well-constrained to measurements of AMPK activity using recently developed AMPK biosensors. As an application of the new model, we predicted AMPK activity in response to exercise-like stimuli. We found that AMPK acts as a time- and exercise-dependent integrator of its input. Our results highlight how uncertainty quantification can facilitate model development and address epistemic uncertainty in a complex signaling pathway, such as AMPK. This work shows the potential for future applications of uncertainty quantification in systems biology to drive new biological insights by incorporating state-of-the-art experimental data at all stages of model development.

systems biology↗

Increasing certainty in systems biology models using Bayesian multimodel inference

Mathematical models are indispensable to the system biology toolkit for studying the structure and behavior of intracellular signaling networks. A common approach to modeling is to develop a system of equations that encode the known biology using approximations and simplifying assumptions. As a result, the same signaling pathway can be represented by multiple models, each with its set of underlying assumptions, which opens up challenges for model selection and decreases certainty in model predictions. Here, we use Bayesian multimodel inference to develop a framework to increase certainty in systems biology models. Using models of the extracellular regulated kinase (ERK) pathway, we first show that multimodel inference increases predictive certainty and yields predictors that are robust to changes in the set of available models. We then show that predictions made with multi-model inference are robust to data uncertainties introduced by decreasing the measurement duration and reducing the sample size. Finally, we use multimodel inference to identify a new model to explain experimentally measured sub-cellular location-specific ERK activity dynamics. In summary, our framework highlights multimodel inference as a disciplined approach to increasing the certainty of intracellular signaling activity predictions.

systems biology↗