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Interpreting the lipidome: bioinformatic approaches to embrace the complexity

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Abstract

Background

Improvements in mass spectrometry (MS) technologies coupled with bioinformatics developments have allowed considerable advancement in the measurement and interpretation of lipidomics data in recent years. Since research areas employing lipidomics are rapidly increasing, there is a great need for bioinformatic tools that capture and utilize the complexity of the data. Currently, the diversity and complexity within the lipidome is often concealed by summing over or averaging individual lipids up to (sub)class-based descriptors, losing valuable information about biological function and interactions with other distinct lipids molecules, proteins and/or metabolites.

Aim of review

To address this gap in knowledge, novel bioinformatics methods are needed to improve identification, quantification, integration and interpretation of lipidomics data. The purpose of this mini-review is to summarize exemplary methods to explore the complexity of the lipidome.

Key scientific concepts of review

Here we describe six approaches that capture three core focus areas for lipidomics: (1) lipidome annotation including a resolvable database identifier, (2) interpretation via pathway- and enrichment-based methods, and (3) understanding complex interactions to emphasize specific steps in the analytical process and highlight challenges in analyses associated with the complexity of lipidome data.

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Acknowledgements

BJWR, JK and GC were supported by Pacific Northwest National Laboratory (PNNL). PNNL is operated for the Department of Energy by Battelle Memorial Institute under Contract DE-AC05-76RLO1830. MF and ZN received financial support from the German Federal Ministry of Education and Research (BMBF) within the framework of the e:Med research and funding concept for SysMedOS Project is gratefully acknowledged.

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Correspondence to Bobbie-Jo M. Webb-Robertson.

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Conflict of interest

All authors have no conflicts of interest to declare that are relevant to the content of this article.

Ethical approval

This review is a retrospective analysis of existing tools and databases and therefore approval by the Research Ethics Committees were not applicable.

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Kyle, J.E., Aimo, L., Bridge, A.J. et al. Interpreting the lipidome: bioinformatic approaches to embrace the complexity. Metabolomics 17, 55 (2021). https://doi.org/10.1007/s11306-021-01802-6

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  • DOI: https://doi.org/10.1007/s11306-021-01802-6

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