Automated Sequential Derivatization for Gas Chromatography-[Orbitrap] Mass Spectrometry-based Metabolite Profiling of Human Blood-based Samples
Many small molecules require derivatization to increase their volatility and to be amenable to gas chromatographic (GC) separation. Derivatization is usually time-consuming, and typical batch-wise procedures increase sample variability. Sequential automation of derivatization via robotic liquid handling enables the overlapping of sample preparation and analysis, maximizing time efficiency and minimizing variability. Herein, a protocol for the fully automated, two-stage derivatization of human blood-based samples in line with GC-[Orbitrap] mass spectrometry (MS)-based metabolomics is described. The protocol delivers a sample-to-sample runtime of 31 min, being suitable for better throughput routine metabolomic analysis. Key features • Direct and rapid methoximation on vial followed by silylation of metabolites in various blood matrices. • Measure ~40 samples per 24 h, identifying > 70 metabolites. • Quantitative reproducibility of routinely measured metabolites with coefficients of variation (CVs) < 30%. • Requires a Thermo Scientific<sup>TM</sup> TriPlus<sup>TM</sup> RSH (or comparable) autosampler equipped with incubator/agitator, cooled drawer, and automatic tool change (ATC) station equipped with liquid handling tools. Graphical overview Workflow for profiling metabolites in human blood using automated derivatization.
Authors
- Jana Klánová (ORCID: https://orcid.org/0000-0002-8818-5307)
- Manuela Bergna
- Renzo Picenoni
- Elliott J. Price (ORCID: https://orcid.org/0000-0001-5691-7000)
- Moira Zanaboni
- Kateřina Coufalíková (ORCID: https://orcid.org/0000-0002-1252-2266)
- Akrem Jbebli
Institutions
- Masaryk University (CZ)
Publication Details
- Journal
- BIO-PROTOCOL
- Published
- 2025-01-01
- DOI
- https://doi.org/10.21769/bioprotoc.5196
- Citations
- 1
- Primary Topic
- Metabolomics and Mass Spectrometry Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.81