Projects per year
Abstract
Background: Different types of analytical methods, with different characteristics, are applied in metabolomics and lipidomics research and include untargeted, targeted and semi-targeted methods. Ultra High Performance Liquid Chromatography-Mass Spectrometry is one of the most frequently applied measurement instruments in metabolomics because of its ability to detect a large number of water-soluble and lipid metabolites over a wide range of concentrations in short analysis times. Methods applied for the detection and quantification of metabolites differ and can either report a (normalised) peak area or an absolute concentration.
Aim of review: In this tutorial we aim to (1) define similarities and differences between different analytical approaches applied in metabolomics and (2) define how amounts or absolute concentrations of endogenous metabolites can be determined together with the advantages and limitations of each approach in relation to the accuracy and precision when concentrations are reported.
Key scientific concepts of review: The pre-analysis knowledge of metabolites to be targeted, the requirement for (normalised) peak responses or absolute concentrations to be reported and the number of metabolites to be reported define whether an untargeted, targeted or semi-targeted method is applied. Fully untargeted methods can only provide (normalised) peak responses and fold changes which can be reported even when the structural identity of the metabolite is not known. Targeted methods, where the analytes are known prior to the analysis, can also report fold changes. Semi-targeted methods apply a mix of characteristics of both untargeted and targeted assays. For the reporting of absolute concentrations of metabolites, the analytes are not only predefined but optimized analytical methods should be developed and validated for each analyte so that the accuracy and precision of concentration data collected for biological samples can be reported as fit for purpose and be reviewed by the scientific community.
Aim of review: In this tutorial we aim to (1) define similarities and differences between different analytical approaches applied in metabolomics and (2) define how amounts or absolute concentrations of endogenous metabolites can be determined together with the advantages and limitations of each approach in relation to the accuracy and precision when concentrations are reported.
Key scientific concepts of review: The pre-analysis knowledge of metabolites to be targeted, the requirement for (normalised) peak responses or absolute concentrations to be reported and the number of metabolites to be reported define whether an untargeted, targeted or semi-targeted method is applied. Fully untargeted methods can only provide (normalised) peak responses and fold changes which can be reported even when the structural identity of the metabolite is not known. Targeted methods, where the analytes are known prior to the analysis, can also report fold changes. Semi-targeted methods apply a mix of characteristics of both untargeted and targeted assays. For the reporting of absolute concentrations of metabolites, the analytes are not only predefined but optimized analytical methods should be developed and validated for each analyte so that the accuracy and precision of concentration data collected for biological samples can be reported as fit for purpose and be reviewed by the scientific community.
Original language | English |
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Article number | 95 |
Number of pages | 19 |
Journal | Metabolomics |
Volume | 20 |
Issue number | 5 |
Early online date | 7 Aug 2024 |
DOIs | |
Publication status | E-pub ahead of print - 7 Aug 2024 |
Keywords
- Quantification
- Untargeted
- Targeted
- UHPLC-MS
- Metabolomics
- Validation
- Semi-targeted
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- 2 Finished
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Standardised metabolite annotation workflows for enhanced biological interpretation in metabolomic data repositories
Dunn, W. (Principal Investigator)
Biotechnology & Biological Sciences Research Council
1/04/20 → 31/03/23
Project: Research Councils
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UK Consortium for Metabolic Phenotyping (MAP UK)
Viant, M. (Principal Investigator), Southam, A. (Researcher), Weber, R. (Researcher) & Dunn, W. (Co-Investigator)
1/06/19 → 31/05/24
Project: Research Councils