The dynamic properties of enzymatic reaction networks (ERNs) are difficult to predict due to the emergence of allosteric interactions, product inhibitions and the competition for resources, that all only materialize once the networks have been assembled. Combining experimental kinetics studies with computational modelling allows us to extract information on these emergent dynamic properties and build predictive models. Here, we utilized the pentose phosphate pathway to demonstrate that previously reported approaches to construct maximally informative datasets can be significantly improved by pulsing both enzymes and substrates into microfluidic flow reactors (instead of substrates only). Our method augments information available from online databases, to map the emergent dynamic behaviours of a network.
No takes yet. Share an insight, caveat, or question.
Jakštaitė et al. (2024) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: