TY - JOUR
T1 - Predicting metabolic fluxes from omics data via machine learning
T2 - Moving from knowledge-driven towards data-driven approaches
AU - Gonçalves, Daniel M.
AU - Henriques, Rui
AU - Costa, Rafael S.
N1 - Funding Information:
info:eu-repo/grantAgreement/FCT//2022.12633.BD/PT#
info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F50006%2F2020/PT#
info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDP%2F50006%2F2020/PT#
info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F50021%2F2020/PT#
info:eu-repo/grantAgreement/FCT/CEEC IND 2017/CEECIND%2F01399%2F2017%2FCP1462%2FCT0015/PT#
The authors also wish to acknowledge the European Union's Horizon BioLaMer project under grant agreement number [ 101099487 ].
Publisher Copyright:
© 2023 The Authors
PY - 2023/10/17
Y1 - 2023/10/17
N2 - The accurate prediction of phenotypes in microorganisms is a main challenge for systems biology. Genome-scale models (GEMs) are a widely used mathematical formalism for predicting metabolic fluxes using constraint-based modeling methods such as flux balance analysis (FBA). However, they require prior knowledge of the metabolic network of an organism and appropriate objective functions, often hampering the prediction of metabolic fluxes under different conditions. Moreover, the integration of omics data to improve the accuracy of phenotype predictions in different physiological states is still in its infancy. Here, we present a novel approach for predicting fluxes under various conditions. We explore the use of supervised machine learning (ML) models using transcriptomics and/or proteomics data and compare their performance against the standard parsimonious FBA (pFBA) approach using case studies of Escherichia coli organism as an example. Our results show that the proposed omics-based ML approach is promising to predict both internal and external metabolic fluxes with smaller prediction errors in comparison to the pFBA approach. The code, data, and detailed results are available at the project's repository [1].
AB - The accurate prediction of phenotypes in microorganisms is a main challenge for systems biology. Genome-scale models (GEMs) are a widely used mathematical formalism for predicting metabolic fluxes using constraint-based modeling methods such as flux balance analysis (FBA). However, they require prior knowledge of the metabolic network of an organism and appropriate objective functions, often hampering the prediction of metabolic fluxes under different conditions. Moreover, the integration of omics data to improve the accuracy of phenotype predictions in different physiological states is still in its infancy. Here, we present a novel approach for predicting fluxes under various conditions. We explore the use of supervised machine learning (ML) models using transcriptomics and/or proteomics data and compare their performance against the standard parsimonious FBA (pFBA) approach using case studies of Escherichia coli organism as an example. Our results show that the proposed omics-based ML approach is promising to predict both internal and external metabolic fluxes with smaller prediction errors in comparison to the pFBA approach. The code, data, and detailed results are available at the project's repository [1].
KW - Flux balance analysis
KW - Genome-scale models
KW - Metabolic fluxes
KW - Omics data
KW - Supervised machine learning
KW - Systems biology
UR - http://www.scopus.com/inward/record.url?scp=85174449267&partnerID=8YFLogxK
U2 - 10.1016/j.csbj.2023.10.002
DO - 10.1016/j.csbj.2023.10.002
M3 - Article
C2 - 37876626
AN - SCOPUS:85174449267
SN - 2001-0370
VL - 21
SP - 4960
EP - 4973
JO - Computational and Structural Biotechnology Journal
JF - Computational and Structural Biotechnology Journal
ER -