Identification of molecular species of glycerophospholipids and sphingomyelin using electrospray mass spectrometry

J. L. Kerwin, Amy Tuininga, L. H. Ericsson

Research output: Contribution to journalArticle

260 Citations (Scopus)

Abstract

This paper describes the use of positive and negative ion electrospray mass spectrometry (MS) and MS/MS (tandem mass spectrometry) to identify glycerophospholipid and ceramide headgroups and their alkyl, alkenyl and acyl constituents. Molecular ion adducts were the primary products formed by positive ionization, occurring as [M + H] + , [M + Na] + , [M + K] + , [M + formate] + , or [M + acetate] + , depending upon the class of glycerophospholipid and the presence or absence of these ionization-promoting species. Similar (negatively charged) ions corresponding to the loss of the groups listed above were formed in negative ion MS. Positive ion electrospray Ms/MS provides information on the nature of the headgroup, with the formation of an ion corresponding to the headgroup itself, or the loss of the headgroup from the molecular ion H + or Na + adduct. Acyl constituents are identified during negative ion MS/MS from the formation of their RCOO - ions. The nature of alkyl or alkenyl substituents in glycerophosphoethanolamine (PE) molecular species can be identified from residual ions following the loss of ethanolamine plus loss of the acyl moiety in the sn-2 position, and cyclization of a phosphate oxygen with C-2 of glycerol. In glycerophosphoinositol (PI) species, it appears that an RCO - ion is formed during negative ion MS/MS, possibly to steric interference from the bulky phosphoinositol headgroup that prevents cyclization (and subsequent stabilization) of the ion described for PE species. Positive and negative ion electrospray MS spectra for molecular species of commercial preparations of PE, PI, phosphatidylserine (PS), glycerophosphocholine (PC) and sphingomyelin (SM) produced similar profiles. For phospholipids occurring as Na + adducts, concentrations above ca. 1 ng/μl produced significant quantities of both [M + H] + and [M + Na] + ions for those molecular species present in the largest quantities, complicating interpretation of the spectra. Complete profiles of molecular species were obtained from as little as 10 picograms of material. Major components of PE were identified from 0.1 picogram total lipid. Using single ion monitoring of the Na + adduct of β-acetyl-γ-O-hexadecyl L-α- phosphatidylcholine, 10 femtograms of material was detected. A mixture of 1 nanogram each of PE, PI, PS, and PC was readily resolved into individual molecular species, with little apparent loss of resolution or preferential ionization. Electrospray MS did not provide information on the position (sn- 1 or sn-2) of fatty acids, and was not capable of differentiating in all instances between alkyl-acyl and alkenyl-acyl substituents without prior separation of these lipid subclasses. Although not reported on in detail, molecular species of other classes of lipids and phospholipids including glycolipids, phosphatidylglycerol, and mono- and dimethylphosphatidylethanolamine can also be analyzed using these techniques. Electrospray MS and MS/MS provides a rapid, sensitive and quantitative alternative to previously published methods for analyses of molecular species.

Original languageEnglish
Pages (from-to)1102-1114
Number of pages13
JournalJournal of Lipid Research
Volume35
Issue number6
StatePublished - 1 Jan 1994

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Glycerophospholipids
Sphingomyelins
Mass spectrometry
Mass Spectrometry
Ions
Tandem Mass Spectrometry
Negative ions
Ionization
formic acid
Positive ions
Phosphatidylserines
Cyclization
Lipids
Phospholipids
Phosphatidylglycerols
Ethanolamine
Ceramides
Glycolipids

Keywords

  • ceramides
  • glyceroph osphoinositol
  • glycerophosphocholine
  • glycerophosphoethanolamine
  • phosphatidylserine

Cite this

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title = "Identification of molecular species of glycerophospholipids and sphingomyelin using electrospray mass spectrometry",
abstract = "This paper describes the use of positive and negative ion electrospray mass spectrometry (MS) and MS/MS (tandem mass spectrometry) to identify glycerophospholipid and ceramide headgroups and their alkyl, alkenyl and acyl constituents. Molecular ion adducts were the primary products formed by positive ionization, occurring as [M + H] + , [M + Na] + , [M + K] + , [M + formate] + , or [M + acetate] + , depending upon the class of glycerophospholipid and the presence or absence of these ionization-promoting species. Similar (negatively charged) ions corresponding to the loss of the groups listed above were formed in negative ion MS. Positive ion electrospray Ms/MS provides information on the nature of the headgroup, with the formation of an ion corresponding to the headgroup itself, or the loss of the headgroup from the molecular ion H + or Na + adduct. Acyl constituents are identified during negative ion MS/MS from the formation of their RCOO - ions. The nature of alkyl or alkenyl substituents in glycerophosphoethanolamine (PE) molecular species can be identified from residual ions following the loss of ethanolamine plus loss of the acyl moiety in the sn-2 position, and cyclization of a phosphate oxygen with C-2 of glycerol. In glycerophosphoinositol (PI) species, it appears that an RCO - ion is formed during negative ion MS/MS, possibly to steric interference from the bulky phosphoinositol headgroup that prevents cyclization (and subsequent stabilization) of the ion described for PE species. Positive and negative ion electrospray MS spectra for molecular species of commercial preparations of PE, PI, phosphatidylserine (PS), glycerophosphocholine (PC) and sphingomyelin (SM) produced similar profiles. For phospholipids occurring as Na + adducts, concentrations above ca. 1 ng/μl produced significant quantities of both [M + H] + and [M + Na] + ions for those molecular species present in the largest quantities, complicating interpretation of the spectra. Complete profiles of molecular species were obtained from as little as 10 picograms of material. Major components of PE were identified from 0.1 picogram total lipid. Using single ion monitoring of the Na + adduct of β-acetyl-γ-O-hexadecyl L-α- phosphatidylcholine, 10 femtograms of material was detected. A mixture of 1 nanogram each of PE, PI, PS, and PC was readily resolved into individual molecular species, with little apparent loss of resolution or preferential ionization. Electrospray MS did not provide information on the position (sn- 1 or sn-2) of fatty acids, and was not capable of differentiating in all instances between alkyl-acyl and alkenyl-acyl substituents without prior separation of these lipid subclasses. Although not reported on in detail, molecular species of other classes of lipids and phospholipids including glycolipids, phosphatidylglycerol, and mono- and dimethylphosphatidylethanolamine can also be analyzed using these techniques. Electrospray MS and MS/MS provides a rapid, sensitive and quantitative alternative to previously published methods for analyses of molecular species.",
keywords = "ceramides, glyceroph osphoinositol, glycerophosphocholine, glycerophosphoethanolamine, phosphatidylserine",
author = "Kerwin, {J. L.} and Amy Tuininga and Ericsson, {L. H.}",
year = "1994",
month = "1",
day = "1",
language = "English",
volume = "35",
pages = "1102--1114",
journal = "Journal of Lipid Research",
issn = "0022-2275",
publisher = "American Society for Biochemistry and Molecular Biology Inc.",
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}

Identification of molecular species of glycerophospholipids and sphingomyelin using electrospray mass spectrometry. / Kerwin, J. L.; Tuininga, Amy; Ericsson, L. H.

In: Journal of Lipid Research, Vol. 35, No. 6, 01.01.1994, p. 1102-1114.

Research output: Contribution to journalArticle

TY - JOUR

T1 - Identification of molecular species of glycerophospholipids and sphingomyelin using electrospray mass spectrometry

AU - Kerwin, J. L.

AU - Tuininga, Amy

AU - Ericsson, L. H.

PY - 1994/1/1

Y1 - 1994/1/1

N2 - This paper describes the use of positive and negative ion electrospray mass spectrometry (MS) and MS/MS (tandem mass spectrometry) to identify glycerophospholipid and ceramide headgroups and their alkyl, alkenyl and acyl constituents. Molecular ion adducts were the primary products formed by positive ionization, occurring as [M + H] + , [M + Na] + , [M + K] + , [M + formate] + , or [M + acetate] + , depending upon the class of glycerophospholipid and the presence or absence of these ionization-promoting species. Similar (negatively charged) ions corresponding to the loss of the groups listed above were formed in negative ion MS. Positive ion electrospray Ms/MS provides information on the nature of the headgroup, with the formation of an ion corresponding to the headgroup itself, or the loss of the headgroup from the molecular ion H + or Na + adduct. Acyl constituents are identified during negative ion MS/MS from the formation of their RCOO - ions. The nature of alkyl or alkenyl substituents in glycerophosphoethanolamine (PE) molecular species can be identified from residual ions following the loss of ethanolamine plus loss of the acyl moiety in the sn-2 position, and cyclization of a phosphate oxygen with C-2 of glycerol. In glycerophosphoinositol (PI) species, it appears that an RCO - ion is formed during negative ion MS/MS, possibly to steric interference from the bulky phosphoinositol headgroup that prevents cyclization (and subsequent stabilization) of the ion described for PE species. Positive and negative ion electrospray MS spectra for molecular species of commercial preparations of PE, PI, phosphatidylserine (PS), glycerophosphocholine (PC) and sphingomyelin (SM) produced similar profiles. For phospholipids occurring as Na + adducts, concentrations above ca. 1 ng/μl produced significant quantities of both [M + H] + and [M + Na] + ions for those molecular species present in the largest quantities, complicating interpretation of the spectra. Complete profiles of molecular species were obtained from as little as 10 picograms of material. Major components of PE were identified from 0.1 picogram total lipid. Using single ion monitoring of the Na + adduct of β-acetyl-γ-O-hexadecyl L-α- phosphatidylcholine, 10 femtograms of material was detected. A mixture of 1 nanogram each of PE, PI, PS, and PC was readily resolved into individual molecular species, with little apparent loss of resolution or preferential ionization. Electrospray MS did not provide information on the position (sn- 1 or sn-2) of fatty acids, and was not capable of differentiating in all instances between alkyl-acyl and alkenyl-acyl substituents without prior separation of these lipid subclasses. Although not reported on in detail, molecular species of other classes of lipids and phospholipids including glycolipids, phosphatidylglycerol, and mono- and dimethylphosphatidylethanolamine can also be analyzed using these techniques. Electrospray MS and MS/MS provides a rapid, sensitive and quantitative alternative to previously published methods for analyses of molecular species.

AB - This paper describes the use of positive and negative ion electrospray mass spectrometry (MS) and MS/MS (tandem mass spectrometry) to identify glycerophospholipid and ceramide headgroups and their alkyl, alkenyl and acyl constituents. Molecular ion adducts were the primary products formed by positive ionization, occurring as [M + H] + , [M + Na] + , [M + K] + , [M + formate] + , or [M + acetate] + , depending upon the class of glycerophospholipid and the presence or absence of these ionization-promoting species. Similar (negatively charged) ions corresponding to the loss of the groups listed above were formed in negative ion MS. Positive ion electrospray Ms/MS provides information on the nature of the headgroup, with the formation of an ion corresponding to the headgroup itself, or the loss of the headgroup from the molecular ion H + or Na + adduct. Acyl constituents are identified during negative ion MS/MS from the formation of their RCOO - ions. The nature of alkyl or alkenyl substituents in glycerophosphoethanolamine (PE) molecular species can be identified from residual ions following the loss of ethanolamine plus loss of the acyl moiety in the sn-2 position, and cyclization of a phosphate oxygen with C-2 of glycerol. In glycerophosphoinositol (PI) species, it appears that an RCO - ion is formed during negative ion MS/MS, possibly to steric interference from the bulky phosphoinositol headgroup that prevents cyclization (and subsequent stabilization) of the ion described for PE species. Positive and negative ion electrospray MS spectra for molecular species of commercial preparations of PE, PI, phosphatidylserine (PS), glycerophosphocholine (PC) and sphingomyelin (SM) produced similar profiles. For phospholipids occurring as Na + adducts, concentrations above ca. 1 ng/μl produced significant quantities of both [M + H] + and [M + Na] + ions for those molecular species present in the largest quantities, complicating interpretation of the spectra. Complete profiles of molecular species were obtained from as little as 10 picograms of material. Major components of PE were identified from 0.1 picogram total lipid. Using single ion monitoring of the Na + adduct of β-acetyl-γ-O-hexadecyl L-α- phosphatidylcholine, 10 femtograms of material was detected. A mixture of 1 nanogram each of PE, PI, PS, and PC was readily resolved into individual molecular species, with little apparent loss of resolution or preferential ionization. Electrospray MS did not provide information on the position (sn- 1 or sn-2) of fatty acids, and was not capable of differentiating in all instances between alkyl-acyl and alkenyl-acyl substituents without prior separation of these lipid subclasses. Although not reported on in detail, molecular species of other classes of lipids and phospholipids including glycolipids, phosphatidylglycerol, and mono- and dimethylphosphatidylethanolamine can also be analyzed using these techniques. Electrospray MS and MS/MS provides a rapid, sensitive and quantitative alternative to previously published methods for analyses of molecular species.

KW - ceramides

KW - glyceroph osphoinositol

KW - glycerophosphocholine

KW - glycerophosphoethanolamine

KW - phosphatidylserine

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JO - Journal of Lipid Research

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