Interpreting the lipidome: bioinformatic approaches to embrace the complexity

Metabolomics - Tập 17 - Trang 1-10 - 2021
Jennifer E. Kyle1, Lucila Aimo2, Alan J. Bridge2, Geremy Clair1, Maria Fedorova3, J. Bernd Helms4, Martijn R. Molenaar5, Zhixu Ni3, Matej Orešič6,7, Denise Slenter8, Egon Willighagen8, Bobbie-Jo M. Webb-Robertson1
1Biological Sciences Division, Pacific Northwest National Laboratory, Richland, USA
2Swiss-Prot Group, SIB Swiss Institute of Bioinformatics, Geneva 4, Switzerland
3Institute of Bioanalytical Chemistry, Faculty of Chemistry and Mineralogy, Center for Biotechnology and Biomedicine, Universität Leipzig, Leipzig, Germany
4Department of Biomolecular Health Sciences, Faculty of Veterinary Medicine, Utrecht University, Utrecht, The Netherlands
5Structural and Computational Biology Unit, European Molecular Biology Laboratory, Heidelberg, Germany
6School of Medical Sciences, Örebro University, Örebro, Sweden
7Turku Bioscience Centre, University of Turku and Åbo Akademi University, Turku, Finland
8Department of Bioinformatics-BiGCaT, NUTRIM, Maastricht University, Maastricht, The Netherlands

Tóm tắt

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. 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. 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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