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Generative Machine Learning Produces Kinetic Models That Accurately Characterize Intracellular Metabolic States

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Journal Nat Catal
Date 2024 Oct 28
PMID 39463726
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Abstract

Generating large omics datasets has become routine for gaining insights into cellular processes, yet deciphering these datasets to determine metabolic states remains challenging. Kinetic models can help integrate omics data by explicitly linking metabolite concentrations, metabolic fluxes and enzyme levels. Nevertheless, determining the kinetic parameters that underlie cellular physiology poses notable obstacles to the widespread use of these mathematical representations of metabolism. Here we present RENAISSANCE, a generative machine learning framework for efficiently parameterizing large-scale kinetic models with dynamic properties matching experimental observations. Through seamless integration of diverse omics data and other relevant information, including extracellular medium composition, physicochemical data and expertise of domain specialists, RENAISSANCE accurately characterizes intracellular metabolic states in . It also estimates missing kinetic parameters and reconciles them with sparse experimental data, substantially reducing parameter uncertainty and improving accuracy. This framework will be valuable for researchers studying metabolic variations involving changes in metabolite and enzyme levels and enzyme activity in health and biotechnology.

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References
1.
Gopalakrishnan S, Dash S, Maranas C . K-FIT: An accelerated kinetic parameterization algorithm using steady-state fluxomic data. Metab Eng. 2020; 61:197-205. DOI: 10.1016/j.ymben.2020.03.001. View

2.
Heckmann D, Lloyd C, Mih N, Ha Y, Zielinski D, Haiman Z . Machine learning applied to enzyme turnover numbers reveals protein structural correlates and improves metabolic models. Nat Commun. 2018; 9(1):5252. PMC: 6286351. DOI: 10.1038/s41467-018-07652-6. View

3.
Miskovic L, Alff-Tuomala S, Soh K, Barth D, Salusjarvi L, Pitkanen J . A design-build-test cycle using modeling and experiments reveals interdependencies between upper glycolysis and xylose uptake in recombinant and improves predictive capabilities of large-scale kinetic models. Biotechnol Biofuels. 2017; 10:166. PMC: 5485749. DOI: 10.1186/s13068-017-0838-5. View

4.
Kummel A, Panke S, Heinemann M . Putative regulatory sites unraveled by network-embedded thermodynamic analysis of metabolome data. Mol Syst Biol. 2006; 2:2006.0034. PMC: 1681506. DOI: 10.1038/msb4100074. View

5.
Hameri T, Fengos G, Ataman M, Miskovic L, Hatzimanikatis V . Kinetic models of metabolism that consider alternative steady-state solutions of intracellular fluxes and concentrations. Metab Eng. 2018; 52:29-41. DOI: 10.1016/j.ymben.2018.10.005. View