Álvaro Altamirano , Ignacio Tapia , Vicente Acuña , Daniel Garrido , Pedro A. Saa
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METACONE: A scalable framework for exploring the conversion cone of metabolic networks
Elementary Conversion Modes (ECMs) – a subset of Elementary Flux Modes (EFMs) – capture the entire production/consumption potential of a metabolic network, providing a more practical view of its interactions with the environment. Despite its reduced size, the set of ECMs is too large for exhaustive enumeration in models reaching genome scale. To address this limitation, we have developed METACONE (METAbolic Conversion cOne for Network Exploration), a scalable algorithm for the computation of a representative linear basis of the conversion cone, the subspace in which all ECMs lie. Two METACONE variants are proposed based on the solution of a series of linear programs following different heuristics. We evaluated the performance of the variants on metabolic models of different sizes, demonstrating their scalability. We further analyzed the resulting basis to explore metabolic capabilities under different environmental conditions in Escherichia coli, identifying metabolic patterns consistent with reported data. Finally, we applied the algorithm to explore metabolic interactions in a microbial consortium of Phocaeicola dorei and Lachnoclostridium symbiosum, recapitulating known cross-feeding interactions and suggesting new possibilities. We envision METACONE as a valuable tool for understanding microbial metabolism in increasingly complex consortia while addressing current scalability challenges.
期刊介绍:
Computational Biology and Chemistry publishes original research papers and review articles in all areas of computational life sciences. High quality research contributions with a major computational component in the areas of nucleic acid and protein sequence research, molecular evolution, molecular genetics (functional genomics and proteomics), theory and practice of either biology-specific or chemical-biology-specific modeling, and structural biology of nucleic acids and proteins are particularly welcome. Exceptionally high quality research work in bioinformatics, systems biology, ecology, computational pharmacology, metabolism, biomedical engineering, epidemiology, and statistical genetics will also be considered.
Given their inherent uncertainty, protein modeling and molecular docking studies should be thoroughly validated. In the absence of experimental results for validation, the use of molecular dynamics simulations along with detailed free energy calculations, for example, should be used as complementary techniques to support the major conclusions. Submissions of premature modeling exercises without additional biological insights will not be considered.
Review articles will generally be commissioned by the editors and should not be submitted to the journal without explicit invitation. However prospective authors are welcome to send a brief (one to three pages) synopsis, which will be evaluated by the editors.