Quantitation of isobaric phosphatidylcholine species in human plasma using a hybrid quadrupole linear ion-trap mass spectrometer[S]

Phosphatidylcholine (PC) species in human plasma are used as biomarkers of disease. PC biomarkers are often limited by the inability to separate isobaric PCs. In this work, we developed a targeted shotgun approach for analysis of isobaric and isomeric PCs. This approach is comprised of two MS method...

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Main Authors: Petr Zacek, Michael Bukowski, Thad A. Rosenberger, Matthew Picklo
Format: Article
Language:English
Published: Elsevier 2016-12-01
Series:Journal of Lipid Research
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0022227520345491
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spelling doaj-a9ce52450c5049a2b220045ce11986e62021-04-29T04:37:49ZengElsevierJournal of Lipid Research0022-22752016-12-01571222252234Quantitation of isobaric phosphatidylcholine species in human plasma using a hybrid quadrupole linear ion-trap mass spectrometer[S]Petr Zacek0Michael Bukowski1Thad A. Rosenberger2Matthew Picklo3To whom correspondence should be addressed.; USDA-ARS Grand Forks Human Nutrition Research Center, Grand Forks, ND 58203; Institute of Organic Chemistry and Biochemistry Academy of Sciences of the Czech Republic, 16610 Prague 6, Czech Republic; To whom correspondence should be addressed.USDA-ARS Grand Forks Human Nutrition Research Center, Grand Forks, ND 58203Department of Biomedical Sciences, University of North Dakota School of Medicine and Health Sciences, University of North Dakota; Grand Forks, ND 58201USDA-ARS Grand Forks Human Nutrition Research Center, Grand Forks, ND 58203; Department of Chemistry, University of North Dakota; Grand Forks, ND 58201Phosphatidylcholine (PC) species in human plasma are used as biomarkers of disease. PC biomarkers are often limited by the inability to separate isobaric PCs. In this work, we developed a targeted shotgun approach for analysis of isobaric and isomeric PCs. This approach is comprised of two MS methods: a precursor ion scanning (PIS) of mass m/z 184 in positive mode (PIS m/z +184) and MS3 fragmentation in negative mode, both performed on the same instrument, a hybrid triple quadrupole ion-trap mass spectrometer. The MS3 experiment identified the FA composition and the relative abundance of isobaric and sn-1, sn-2 positional isomeric PC species, which were subsequently combined with absolute quantitative data obtained by PIS m/z +184 scan. This approach was applied to the analysis of a National Institute of Standards and Technology human blood plasma standard reference material (SRM 1950). We quantified more than 70 PCs and confirmed that a majority are present in isobaric and isomeric mixtures. The FA content determined by this method was comparable to that obtained using GC with flame ionization detection, supporting the quantitative nature of this MS method. This methodology will provide more in-depth biomarker information for clinical and mechanistic studies.http://www.sciencedirect.com/science/article/pii/S0022227520345491triple quadrupole/ion-trapNational Institute of Standards and Technology human blood plasmamass spectrometryshotgun lipidomicsdocosahexaenoic acid
collection DOAJ
language English
format Article
sources DOAJ
author Petr Zacek
Michael Bukowski
Thad A. Rosenberger
Matthew Picklo
spellingShingle Petr Zacek
Michael Bukowski
Thad A. Rosenberger
Matthew Picklo
Quantitation of isobaric phosphatidylcholine species in human plasma using a hybrid quadrupole linear ion-trap mass spectrometer[S]
Journal of Lipid Research
triple quadrupole/ion-trap
National Institute of Standards and Technology human blood plasma
mass spectrometry
shotgun lipidomics
docosahexaenoic acid
author_facet Petr Zacek
Michael Bukowski
Thad A. Rosenberger
Matthew Picklo
author_sort Petr Zacek
title Quantitation of isobaric phosphatidylcholine species in human plasma using a hybrid quadrupole linear ion-trap mass spectrometer[S]
title_short Quantitation of isobaric phosphatidylcholine species in human plasma using a hybrid quadrupole linear ion-trap mass spectrometer[S]
title_full Quantitation of isobaric phosphatidylcholine species in human plasma using a hybrid quadrupole linear ion-trap mass spectrometer[S]
title_fullStr Quantitation of isobaric phosphatidylcholine species in human plasma using a hybrid quadrupole linear ion-trap mass spectrometer[S]
title_full_unstemmed Quantitation of isobaric phosphatidylcholine species in human plasma using a hybrid quadrupole linear ion-trap mass spectrometer[S]
title_sort quantitation of isobaric phosphatidylcholine species in human plasma using a hybrid quadrupole linear ion-trap mass spectrometer[s]
publisher Elsevier
series Journal of Lipid Research
issn 0022-2275
publishDate 2016-12-01
description Phosphatidylcholine (PC) species in human plasma are used as biomarkers of disease. PC biomarkers are often limited by the inability to separate isobaric PCs. In this work, we developed a targeted shotgun approach for analysis of isobaric and isomeric PCs. This approach is comprised of two MS methods: a precursor ion scanning (PIS) of mass m/z 184 in positive mode (PIS m/z +184) and MS3 fragmentation in negative mode, both performed on the same instrument, a hybrid triple quadrupole ion-trap mass spectrometer. The MS3 experiment identified the FA composition and the relative abundance of isobaric and sn-1, sn-2 positional isomeric PC species, which were subsequently combined with absolute quantitative data obtained by PIS m/z +184 scan. This approach was applied to the analysis of a National Institute of Standards and Technology human blood plasma standard reference material (SRM 1950). We quantified more than 70 PCs and confirmed that a majority are present in isobaric and isomeric mixtures. The FA content determined by this method was comparable to that obtained using GC with flame ionization detection, supporting the quantitative nature of this MS method. This methodology will provide more in-depth biomarker information for clinical and mechanistic studies.
topic triple quadrupole/ion-trap
National Institute of Standards and Technology human blood plasma
mass spectrometry
shotgun lipidomics
docosahexaenoic acid
url http://www.sciencedirect.com/science/article/pii/S0022227520345491
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