Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2023 Jan 25:11:1129717.
doi: 10.3389/fchem.2023.1129717. eCollection 2023.

Innovation in identifying metabolites from complex metabolome-Highlights of recent analytical platforms and protocols

Affiliations
Review

Innovation in identifying metabolites from complex metabolome-Highlights of recent analytical platforms and protocols

Shi Qiu et al. Front Chem. .

Abstract

Metabolites are closely intertwined genotypes that can provide clear information about the final phenotype. The high-throughput analysis platform used to identify candidate metabolites and describe their contributions can help to quickly detect metabolic characteristics from large spectral data, which may lead to peak data preprocessing, statistical analysis and functional interpretation. Developing a comprehensive strategy for discovering and verifying bioactive metabolites can provide a large number of new functional biomarkers, and then more closely reveal their functional changes, which has relevant biological significance for disease diagnosis and prognosis treatment.

Keywords: diagnosis; functional biomarkers; metabolic pathway; metabolites; metabolomics.

PubMed Disclaimer

Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

FIGURE 1
FIGURE 1
Analytical workflow of typical metabolomic analysis. It includes several basic steps: experimental design (A), sample collection (B), metabolite profling (C), data analysis (D−F), functional interpretation (G, H) and potential application of the integrated datasets (I). Step (A) The experimental design based on phenotype analysis or diagnosis and treatment. Step (B) Sample preparation through deproteinization and/or centrifugation of biofluids. Step (C) Metabolite separation on a column (chromatography) and detection of analyte signal through MS or NMR spectroscopy. Metabolites can be identified on the basis of a combination of retention time and MS signature. Step (D) The data pre-processing and normalization of raw signals). Then, pattern recognition analysis and computational methods after data collection. Step (E) Expression analysis of the differential metabolites by which data is filtered for significant biomarkers of interest. Heatmap plot shows the differential metabolites in the statistical analysis function. Step (F) Clustering correlation patterns analysis among different data sets. Step (G) Pathway enrichment overview. Circle size and color are based on the pathway size and p-value. Step (H) The enriched metabolism pathway and joint pathway analysis in the correlation network. Step (I) Analysis model of diagnosis, prognosis and treatment based on the candidate metabolite features using classical univariate and multivariate ROC curve analyses. All images were obtained using the example data provided by the MetaboAnalyst 5.0 and figures also created by BioRender.

References

    1. Fu J., Zhang Y., Wang Y., Zhang H., Liu J., Tang J., et al. (2022). Optimization of metabolomic data processing using NOREVA. Nat. Protoc. 17, 129–151. 10.1038/s41596-021-00636-9 - DOI - PubMed
    1. Horvath T. D., Haidacher S. J., Engevik M. A., Luck B., Ruan W., Ihekweazu F., et al. (2022). Interrogation of the mammalian gut-brain axis using LC-MS/MS-based targeted metabolomics with in vitro bacterial and organoid cultures and in vivo gnotobiotic mouse models. Nat. Protoc. 10.1038/s41596-022-00767-7 - DOI - PubMed
    1. Kilgour M. K., MacPherson S., Zacharias L. G., LeBlanc J., Babinszky S., Kowalchuk G., et al. (2022). Principles of reproducible metabolite profiling of enriched lymphocytes in tumors and ascites from human ovarian cancer. Nat. Protoc. 17, 2668–2698. 10.1038/s41596-022-00729-z - DOI - PubMed
    1. Kirkwood K. I., Pratt B. S., Shulman N., Tamura K., MacCoss M. J., MacLean B. X., et al. (2022). Utilizing Skyline to analyze lipidomics data containing liquid chromatography, ion mobility spectrometry and mass spectrometry dimensions. Nat. Protoc. 17, 2415–2430. 10.1038/s41596-022-00714-6 - DOI - PMC - PubMed
    1. Pang Z., Zhou G., Ewald J., Chang L., Hacariz O., Basu N., et al. (2022). Using MetaboAnalyst 5.0 for LC-HRMS spectra processing, multi-omics integration and covariate adjustment of global metabolomics data. Nat. Protoc. 17, 1735–1761. 10.1038/s41596-022-00710-w - DOI - PubMed

LinkOut - more resources