Literature DB >> 19646933

Normal phase liquid chromatography coupled to quadrupole time of flight atmospheric pressure chemical ionization mass spectrometry for separation, detection and mass spectrometric profiling of neutral sphingolipids and cholesterol.

Hany Farwanah1, Jennifer Wirtz, Thomas Kolter, Klaus Raith, Reinhard H H Neubert, Konrad Sandhoff.   

Abstract

Many lipidomic approaches focus on investigating aspects of sphingolipid metabolism. Special emphasis is put on neutral sphingolipids and cholesterol and their interaction. Such an interest is attributed to the fact that those lipids are altered in a series of serious disorders including various sphingolipidoses. High performance thin-layer chromatography (HPTLC) has become a widely used technique for lipid analysis. However, mass spectrometric profiling is irreplaceable for gaining an overview about the various molecular species within a lipid class. In this work we have developed a sensitive method based on a gradient normal phase high performance liquid chromatography (HPLC) coupled to quadrupole time of flight (QTOF) atmospheric pressure chemical ionization mass spectrometry (APCI-MS) in positive mode, which for the first time enables separation, on-line detection, and mass spectrometric profiling of multiple neutral sphingolipids including ceramide, glucosylceramide, lactosylceramide, globotriaosylceramide, globotetraosylceramide, sphingomyelin as well as cholesterol within less than 15min. An important advantage of the presented HPLC/APCI-MS approach is that the separation pattern emulates the one obtained by an optimized HPTLC method with a multiple stage development. Thus, the lipid classes previously separated and quantified by HPTLC can be easily screened regarding their mass spectrometric profiles by HPLC/APCI-MS. In addition, the selected ionization conditions enable in-source fragmentation providing useful structural information. The methods (HPLC/APCI-MS and the optimized HPTLC) were applied for the analysis of the mentioned lipids in human fibroblasts. This approach is aimed basically at investigators who perform studies based on genetic modifications or treatment with pharmacological agents leading to changes in the biochemical pathways of neutral sphingolipids and cholesterol. In addition, it can be of interest for research on disorders related to impairments of sphingolipid metabolism.

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Year:  2009        PMID: 19646933     DOI: 10.1016/j.jchromb.2009.07.008

Source DB:  PubMed          Journal:  J Chromatogr B Analyt Technol Biomed Life Sci        ISSN: 1570-0232            Impact factor:   3.205


  15 in total

Review 1.  Sphingolipid and glycosphingolipid metabolic pathways in the era of sphingolipidomics.

Authors:  Alfred H Merrill
Journal:  Chem Rev       Date:  2011-09-26       Impact factor: 60.622

2.  LC/MS analysis of stratum corneum lipids: ceramide profiling and discovery.

Authors:  Jeroen van Smeden; Louise Hoppel; Rob van der Heijden; Thomas Hankemeier; Rob J Vreeken; Joke A Bouwstra
Journal:  J Lipid Res       Date:  2011-03-28       Impact factor: 5.922

3.  Development and validation of sensitive LC-MS/MS assays for quantification of HP-β-CD in human plasma and CSF.

Authors:  Hui Jiang; Rohini Sidhu; Hideji Fujiwara; Marc De Meulder; Ronald de Vries; Yong Gong; Mark Kao; Forbes D Porter; Nicole M Yanjanin; Nuria Carillo-Carasco; Xin Xu; Elizabeth Ottinger; Myra Woolery; Daniel S Ory; Xuntian Jiang
Journal:  J Lipid Res       Date:  2014-05-27       Impact factor: 5.922

4.  Modifier-concept of colorectal carcinogenesis: lipidomics as a technical tool in pathway analysis.

Authors:  Nikolaus Gassler; Christina Klaus; Elke Kaemmerer; Andrea Reinartz
Journal:  World J Gastroenterol       Date:  2010-04-21       Impact factor: 5.742

5.  A rapid and quantitative LC-MS/MS method to profile sphingolipids.

Authors:  Max Scherer; Kerstin Leuthäuser-Jaschinski; Josef Ecker; Gerd Schmitz; Gerhard Liebisch
Journal:  J Lipid Res       Date:  2010-03-12       Impact factor: 5.922

6.  Nascent high density lipoproteins formed by ABCA1 resemble lipid rafts and are structurally organized by three apoA-I monomers.

Authors:  Mary G Sorci-Thomas; John S Owen; Brian Fulp; Shaila Bhat; Xuewei Zhu; John S Parks; Dharika Shah; W Gray Jerome; Mark Gerelus; Manal Zabalawi; Michael J Thomas
Journal:  J Lipid Res       Date:  2012-06-29       Impact factor: 5.922

Review 7.  An introduction to sphingolipid metabolism and analysis by new technologies.

Authors:  Yanfeng Chen; Ying Liu; M Cameron Sullards; Alfred H Merrill
Journal:  Neuromolecular Med       Date:  2010-08-03       Impact factor: 3.843

Review 8.  Non-alcoholic fatty liver disease: Insights from sphingolipidomics.

Authors:  David J Montefusco; Jeremy C Allegood; Sarah Spiegel; L Ashley Cowart
Journal:  Biochem Biophys Res Commun       Date:  2018-05-21       Impact factor: 3.575

9.  CLN3 loss disturbs membrane microdomain properties and protein transport in brain endothelial cells.

Authors:  Luis Tecedor; Colleen S Stein; Mark L Schultz; Hany Farwanah; Konrad Sandhoff; Beverly L Davidson
Journal:  J Neurosci       Date:  2013-11-13       Impact factor: 6.167

Review 10.  My journey into the world of sphingolipids and sphingolipidoses.

Authors:  Konrad Sandhoff
Journal:  Proc Jpn Acad Ser B Phys Biol Sci       Date:  2012       Impact factor: 3.493

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