Mass spectrometry-based workflow for accurate quantification of E. coli enzymes: how proteomics can play a key role in metabolic engineering.

Abstract : Metabolic engineering aims to design high performance microbial strains producing compounds of interest. This requires systems-level understanding; genome-scale models have therefore been developed to predict metabolic fluxes. However, multi-omics data including genomics, transcriptomics, fluxomics and proteomics may be required to model the metabolism of potential cell factories. Recent technological advances to quantitative proteomics have made mass spectrometry-based quantitative assays an interesting alternative to more traditional immuno-affinity based approaches. This has improved specificity and multiplexing capabilities. In this study we developed a quantification workflow to analyse enzymes involved in central metabolism in Escherichia coli (E. coli). This workflow combined full-length isotopically labelled standards with Selected Reaction Monitoring (SRM) analysis. First, full-length 15N labelled standards were produced and calibrated to ensure accurate measurements. Liquid chromatography conditions were then optimised for reproducibility and multiplexing capabilities over a single 30-minute LC-MS analysis. This workflow was used to accurately quantify 22 enzymes involved in E. coli central metabolism in a wild-type reference strain and two derived strains, optimised for higher NADPH production. In combination with measurements of metabolic fluxes, proteomics data can be used to assess different levels of regulation, in particular enzyme abundance and activity. This provides information which can be used to design specific strains used in biotechnology. In addition, accurate measurement of absolute enzyme concentrations is key to the development of predictive kinetic models in the context of metabolic engineering.
Type de document :
Article dans une revue
Molecular and Cellular Proteomics, American Society for Biochemistry and Molecular Biology, 2014, 13 (4), pp.954-968. 〈10.1074/mcp.M113.032672〉
Liste complète des métadonnées

https://hal.inria.fr/hal-00947196
Contributeur : Hidde De Jong <>
Soumis le : vendredi 14 février 2014 - 18:10:07
Dernière modification le : mardi 3 juillet 2018 - 09:38:03

Lien texte intégral

Identifiants

Collections

Citation

Mathieu Trauchessec, Michel Jaquinod, Aline Bonvalot, Virginie Brun, Christophe Bruley, et al.. Mass spectrometry-based workflow for accurate quantification of E. coli enzymes: how proteomics can play a key role in metabolic engineering.. Molecular and Cellular Proteomics, American Society for Biochemistry and Molecular Biology, 2014, 13 (4), pp.954-968. 〈10.1074/mcp.M113.032672〉. 〈hal-00947196〉

Partager

Métriques

Consultations de la notice

1540