Ionic liquid matrices for MALDI mass spectrometry of lignin
The use of matrix-assisted laser desorption/ionization (MALDI) mass spectrometry for the study of lignin is still extremely limited due to its low ionization efficiency. We have developed an approach for obtaining high-intensity MALDI mass spectra of lignin, based on the use of ionic liquids as matr...
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Veröffentlicht in: | Analytical and bioanalytical chemistry 2018-11, Vol.410 (28), p.7429-7439 |
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Sprache: | eng |
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Zusammenfassung: | The use of matrix-assisted laser desorption/ionization (MALDI) mass spectrometry for the study of lignin is still extremely limited due to its low ionization efficiency. We have developed an approach for obtaining high-intensity MALDI mass spectra of lignin, based on the use of ionic liquids as matrices. Thirty-two ionic liquids consisting of large nitrogen-containing cations and anions of aromatic acids, traditionally used as crystalline matrices, were tested. It was established that ionic liquids based on
N,N
-diisopropyl-
N
-ethylammonium,
N
-isopropyl-
N
-methyl-
N
-
tert
-butylammonium, 3-aminoquinolinium, pyridinium, and 1-methylimidazolium cations and anions of ferulic, α-cyanohydroxycinnamic, and 2,5-dihydroxybenzoic acids as MALDI matrices provided high efficiency of lignin desorption/ionization with generation of singly charged protonated molecules of its oligomers. The use of such matrices in combination with the MALDI quadrupole ion trap–time-of-flight technique allows high-intensity mass spectra of lignin to be obtained without interferences from the matrix in the molecular weight range up to 3 kDa, adequately reflecting the molecular mass characteristics of lignin preparations. Using ionic liquid matrices, MS
2
and MS
3
MALDI mass spectra of lignins for various precursor ions were first obtained, including in the region of large (> 2 kDa) molecular weights. Differences in tandem mass spectra of coniferous and deciduous lignins, reflecting the structural features of corresponding oligomers were demonstrated.
Graphical abstract
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ISSN: | 1618-2642 1618-2650 |
DOI: | 10.1007/s00216-018-1353-7 |