4.6 Article

Assessment of altered lipid homeostasis by HILIC-ion mobility-mass spectrometry-based lipidomics

Journal

JOURNAL OF LIPID RESEARCH
Volume 58, Issue 4, Pages 809-819

Publisher

ELSEVIER
DOI: 10.1194/jlr.D074724

Keywords

liquid chromatography; cholesterol; biosynthesis; phospholipids; collision cross-section; benzalkonium chloride; AY9944; neuro2a cells; hydrophilic interaction liquid chromatography

Funding

  1. National Institutes of Health [R00 HD073270]
  2. University of Washington Center for Exposures, Diseases, Genomics, and Environment (NIH) [P30ES007033]
  3. Department of Medicinal Chemistry in the School of Pharmacy at the University of Washington
  4. National Institutes of Environmental Health Sciences training grant [T32 ES007032]

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Ion mobility-mass spectrometry (IM-MS) has proven to be a highly informative technique for the characterization of lipids from cells and tissues. We report the combination of hydrophilic-interaction liquid chromatography (HILIC) with traveling-wave IM-MS (TWIM-MS) for comprehensive lipidomics analysis. Main lipid categories such as glycerolipids, sphingolipids, and glycerophospholipids are separated on the basis of their lipid backbones in the IM dimension, whereas subclasses of each category are mostly separated on the basis of their headgroups in the HILIC dimension, demonstrating the orthogonality of HILIC and IM separations. Using our previously established lipid calibrants for collision cross-section (CCS) measurements in TWIM, we measured over 250 CCS values covering 12 lipid classes in positive and negative modes. The coverage of the HILIC-IM-MS method is demonstrated in the analysis of Neuro2a neuroblastoma cells exposed to benzalkonium chlorides (BACs) with C10 or C16 alkyl chains, which we have previously shown to affect gene expression related to cholesterol and lipid homeostasis. We found that BAC exposure resulted in significant changes to several lipid classes, including glycerides, sphingomyelins, phosphatidylcholines, and phosphatidylethanolamines. Our results indicate that BAC exposure modifies lipid homeostasis in a manner that is dependent upon the length of the BAC alkyl chain.

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