Published May 2019 | Version v1
Journal article

Modeling the fragmentation patterns of triacylglycerides in mass spectrometry allows the quantification of the regioisomers with a minimal number of standards

  • 1. Laberca, Oniris, INRA, 44307, Nantes (France)
  • 2. UR1268 BIA (Biopolymères Interactions Assemblages), INRA, 44316, Nantes (France)
  • 3. Chemistry Department, University of Massachusetts Boston, Boston, MA, 02125 (United States)

Description

Highlights: • The calibration by using all standards in lipidomics is not possible. • We can identify trends of the behavior of triacylglycerides in MS, and model them. • The predicted behavior can be used to quantify by fitting a few standards. • We modeled the fragmentation of the regioisomers of triacylglycerides. • Their quantification using this model showed good agreement with previous results. -- Abstract: Mass spectrometry allows the relative quantification of the regioisomers of triacylglycerides by the calibration of their fragmentation patterns. However, due to the plethora of regioisomers of triacylglycerides, calibration with every standard is not feasible. An analytical challenge in the field is the prediction of the fragmentation patterns of triacylglycerides to quantify their regioisomers. Thus, we aimed to model these fragmentation patterns to quantify the regioisomeric composition, even for those without commercially available standards. In a first step, we modeled the fragmentation patterns of the regioisomers of triacylglycerides obtained from different published datasets. We found the same qualitative trends of fragmentation beyond differences in the type of adduct in these datasets (both [M+NH4]+ and [M+H]+), and the type of instrument (orbitrap, Q-ToF, ion-trap, single quadrupole, and triple quadrupole). However, the quantitative trends of fragmentation were adduct and instrument specific. From these observations, we modeled quantitatively the common trends of fragmentation of triacylglycerides in every dataset. In a second step, we applied this methodology on a Synapt G2S Q-ToF to quantify the regioisomers of triacylglycerides in sunflower and olive oils. The results of our quantification were in good agreement with previous published quantifications of triacylglycerides, even for regioisomers that were not present in the training dataset. The species with more than two highly unsaturated fatty acids (arachidonic, eicosapentaenoic, and docosahexaenoic acids) showed a complex behavior and lower predictability of their fragmentation patterns. However, this framework presents the capacity to model this behavior when more data are available. It would be also applicable to standardize the quantification of the regioisomers of triacylglycerides in an inter-laboratory ring study.

Additional details

Identifiers

DOI
10.1016/j.aca.2019.01.017;
PII
S000326701930056X;

Publishing Information

Journal Title
Analytica Chimica Acta
Journal Volume
1057
Journal Page Range
p. 60-69
ISSN
0003-2670
CODEN
ACACAM

INIS

Country of Publication
Netherlands
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
55008683
Subject category
S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
Descriptors DEI
CALIBRATION; CARBOXYLIC ACIDS; DATASETS; ISOMERS; MASS SPECTROSCOPY; QUADRUPOLES; SIMULATION; SUNFLOWERS
Descriptors DEC
DOCUMENT TYPES; MAGNOLIOPHYTA; MAGNOLIOPSIDA; MULTIPOLES; ORGANIC ACIDS; ORGANIC COMPOUNDS; PLANTS; SPECTROSCOPY

Optional Information

Copyright
Copyright (c) 2019 Elsevier B.V. All rights reserved.