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Ghorasaini, M.* ; Mohammed, Y.* ; Adamski, J. ; Bettcher, L.* ; Bowden, J.A.* ; Cabruja, M.* ; Contrepois, K.* ; Ellenberger, M.* ; Gajera, B.* ; Haid, M. ; Hornburg, D.* ; Hunter, C.* ; Jones, C.M.* ; Klein, T.* ; Mayboroda, O.* ; Mirzaian, M.* ; Moaddel, R.* ; Ferrucci, L.* ; Lovett, J.* ; Nazir, K.* ; Pearson, M.* ; Ubhi, B.K.* ; Raftery, D.* ; Riols, F. ; Sayers, R.* ; Sijbrands, E.J.G.* ; Snyder, M.P.* ; Su, B.* ; Velagapudi, V.* ; Williams, K.J.* ; de Rijke, Y.B.* ; Giera, M.*

Cross-laboratory standardization of preclinical lipidomics using differential mobility spectrometry and multiple reaction monitoring.

Anal. Chem. 93, 16369-16378 (2021)
Verlagsversion DOI PMC
Open Access Gold (Paid Option)
Creative Commons Lizenzvertrag
Modern biomarker and translational research as well as personalized health care studies rely heavily on powerful omics' technologies, including metabolomics and lipidomics. However, to translate metabolomics and lipidomics discoveries into a high-throughput clinical setting, standardization is of utmost importance. Here, we compared and benchmarked a quantitative lipidomics platform. The employed Lipidyzer platform is based on lipid class separation by means of differential mobility spectrometry with subsequent multiple reaction monitoring. Quantitation is achieved by the use of 54 deuterated internal standards and an automated informatics approach. We investigated the platform performance across nine laboratories using NIST SRM 1950-Metabolites in Frozen Human Plasma, and three NIST Candidate Reference Materials 8231-Frozen Human Plasma Suite for Metabolomics (high triglyceride, diabetic, and African-American plasma). In addition, we comparatively analyzed 59 plasma samples from individuals with familial hypercholesterolemia from a clinical cohort study. We provide evidence that the more practical methyl-tert-butyl ether extraction outperforms the classic Bligh and Dyer approach and compare our results with two previously published ring trials. In summary, we present standardized lipidomics protocols, allowing for the highly reproducible analysis of several hundred human plasma lipids, and present detailed molecular information for potentially disease relevant and ethnicity-related materials.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Korrespondenzautor
Schlagwörter Human Plasma; Extraction; Lipids
ISSN (print) / ISBN 0003-2700
e-ISSN 1520-6882
Zeitschrift Analytical Chemistry
Quellenangaben Band: 93, Heft: 49, Seiten: 16369-16378 Artikelnummer: , Supplement: ,
Verlag American Chemical Society (ACS)
Verlagsort 1155 16th St, Nw, Washington, Dc 20036 Usa
Nichtpatentliteratur Publikationen
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Experimental Genetics (IEG)
CF Metabolomics & Proteomics (CF-MPC)
Förderungen Biocenter Finland
HiLIFE
Intramural Research Program of the National Institute on Aging, NIH
NWO XOmics project
H2020 ITN consortium ArthritisHeal
NIH