Structural Elucidation and Relative Quantification of Fatty Acid Double Bond Positional Isomers in Biological Tissues Enabled by Gas‐Phase Charge Inversion Ion/Ion Reactions

Author:

Bonney Julia R.1,Prentice Boone. M1ORCID

Affiliation:

1. Department of Chemistry University of Florida Gainesville FL 32611 USA

Abstract

AbstractFatty acids (FAs) contain a vast amount of structural diversity, and differences in fatty acid structure have been associated with various disease states. Accurate identification and characterization of fatty acids is critical to fully understand the biochemical roles these compounds play in disease progression. Conventional tandem mass spectrometry (MS/MS) workflows do not provide sufficient structural information, necessitating alternative dissociation methods. Gas‐phase charge inversion ion/ion reactions can be used to alter the ion type subjected to activation to provide improved or complementary structural information. Herein, we have used an ion/ion reaction between fatty acid (FA) anions and magnesium tris‐phenanthroline [Mg(Phen)3] dications to promote charge remote fragmentation of carbon‐carbon bonds along the fatty acid chain, allowing for localization of carbon‐carbon double bond (C=C) positions to successfully differentiate monounsaturated fatty acid isomers. Relative quantification was also performed to obtain the relative abundance of fatty acid isomers in different biological tissues. For example, the relative abundance of FA 18 : 1 (9) was determined to vary across regions of rat brain, rat kidney, and mouse pancreas, and FA 16 : 1 (9) was found to have a higher relative abundance in the dermis layer compared to the sebaceous glands in human skin tissue.

Funder

National Institutes of Health

Publisher

Wiley

Subject

General Medicine

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