Chemoselective detection and discrimination of carbonyl-containing compounds in metabolite mixtures by <sup>1</sup>H-detected <sup>15</sup>N nuclear magnetic resonance

Andrew N. Lane, Sengodagounder Arumugam, Pawel K. Lorkiewicz, Richard M. Higashi, Sébastien Laulhé, Michael H. Nantz, Hunter N B Moseley, Teresa W M Fan

Research output: Contribution to journalArticle

14 Citations (Scopus)

Abstract

NMR spectra of mixtures of metabolites extracted from cells or tissues are extremely complex, reflecting the large number of compounds that are present over a wide range of concentrations. Although multidimensional NMR can greatly improve resolution as well as improve reliability of compound assignments, lower abundance metabolites often remain hidden. We have developed a carbonyl-selective aminooxy probe that specifically reacts with free keto and aldehyde functions, but not carboxylates. By incorporating <sup>15</sup>N in the aminooxy functional group, <sup>15</sup>N-edited NMR was used to select exclusively those metabolites that contain a free carbonyl function while all other metabolites are rejected. Here, we demonstrate that the chemical shifts of the aminooxy adducts of ketones and aldehydes are very different, which can be used to discriminate between aldoses and ketoses, for example. Utilizing the 2-bond or 3-bond <sup>15</sup>N-<sup>1</sup>H couplings, the <sup>15</sup>N-edited NMR analysis was optimized first with authentic standards and then applied to an extract of the lung adenocarcinoma cell line A549. More than 30 carbonyl-containing compounds at NMR-detectable levels, six of which we have assigned by reference to our database. As the aminooxy probe contains a permanently charged quaternary ammonium group, the adducts are also optimized for detection by mass spectrometry. Thus, this sample preparation technique provides a better link between the two structural determination tools, thereby paving the way to faster and more reliable identification of both known and unknown metabolites directly in crude biological extracts.

Original languageEnglish (US)
Pages (from-to)337-343
Number of pages7
JournalMagnetic Resonance in Chemistry
Volume53
Issue number5
DOIs
StatePublished - May 1 2015
Externally publishedYes

Fingerprint

Metabolites
Nuclear magnetic resonance
Aldehydes
Ketoses
Chemical shift
Ketones
Ammonium Compounds
Functional groups
Mass spectrometry
Cells
Tissue

Keywords

  • <sup>15</sup>N-edited <sup>1</sup>H NMR
  • aldehydes
  • aminooxy derivatives
  • chemoselection
  • ketones
  • metabolomics

ASJC Scopus subject areas

  • Chemistry(all)
  • Materials Science(all)

Cite this

Chemoselective detection and discrimination of carbonyl-containing compounds in metabolite mixtures by <sup>1</sup>H-detected <sup>15</sup>N nuclear magnetic resonance. / Lane, Andrew N.; Arumugam, Sengodagounder; Lorkiewicz, Pawel K.; Higashi, Richard M.; Laulhé, Sébastien; Nantz, Michael H.; Moseley, Hunter N B; Fan, Teresa W M.

In: Magnetic Resonance in Chemistry, Vol. 53, No. 5, 01.05.2015, p. 337-343.

Research output: Contribution to journalArticle

Lane, Andrew N. ; Arumugam, Sengodagounder ; Lorkiewicz, Pawel K. ; Higashi, Richard M. ; Laulhé, Sébastien ; Nantz, Michael H. ; Moseley, Hunter N B ; Fan, Teresa W M. / Chemoselective detection and discrimination of carbonyl-containing compounds in metabolite mixtures by <sup>1</sup>H-detected <sup>15</sup>N nuclear magnetic resonance. In: Magnetic Resonance in Chemistry. 2015 ; Vol. 53, No. 5. pp. 337-343.
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AU - Higashi, Richard M.

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