Targeted Metabolomic Methods for <sup>13</sup> C Stable Isotope Labeling with Uniformly Labeled Glucose and Glutamine Using Liquid Chromatography–Tandem Mass Spectrometry (LC–MS/MS)
Heavy carbon labeling has emerged as a popular way to study metabolic diseases. However, most carbon labeling techniques use untargeted mass spectrometry, which typically requires dependence on a research core and specialized software. By combining published <sup>13</sup>C labeling patterns and known enzyme reactions, an optimized targeted mass spectrometry method was generated to measure stable isotope labeling with carbon-13 through glycolysis, the tricarboxylic acid cycle, the hexosamine biosynthetic pathway, and glutaminolysis using uniformly labeled glucose or glutamine. This method provides a novel and adaptable approach to investigate pointed hypotheses on the utilization of glucose or glutamine in disease states and models.
Authors
- Jeffrey C. Rathmell (ORCID: https://orcid.org/0000-0002-4106-3396)
- Erin Q. Jennings (ORCID: https://orcid.org/0000-0002-6991-6098)
- W. Kimryn Rathmell (ORCID: https://orcid.org/0000-0002-4984-0225)
Institutions
- National Institutes of Health (US)
- Center of Molecular Immunology (Cuba) (CU)
- National Institute of Diabetes and Digestive and Kidney Diseases (US)
- Hematology Oncology Associates (US)
- Vanderbilt University Medical Center (US)
Publication Details
- Journal
- Journal of Proteome Research
- Published
- 2025-11-20
- DOI
- https://doi.org/10.1021/acs.jproteome.5c00514
- Citations
- 1
- Primary Topic
- Metabolomics and Mass Spectrometry Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.81