Distinction of amino acid enantiomers based on the basicity of their dimers

K. Vékey, Gábor Czira

Research output: Contribution to journalArticle

86 Citations (Scopus)

Abstract

Mixtures of several amino acid pairs, in all four chiral combinations, were studied. The protonated trimers (A2-BH+) fragment, forming ABH+ and A2H+ dimers. Abundance ratios of these fragments were measured in the mass-analyzed ion kinetic energy spectra of the trimers. These were found to depend on the stereochemistry (homo- or heterochiral form) of the ABH+ dimer. The results were evaluated using the kinetic method, and the chiral discrimination was related to a difference in gas-phase basicity (GB) between the homo- and the heterochiral dimers. Four amino acid pairs (proline-tryptophan, phenylalanine-alanine, phenylalanine-proline, and phenylalanine-valine) were studied. Chiral discriminations were observed in all cases, relating to 0.4-4 kJ/mol differences in GB. The technique described here can generally be used to study enantiomers by mass spectrometry and is capable of reliably distinguishing energy differences as small as 0.2 kJ/mol in cluster ions.

Original languageEnglish
Pages (from-to)1700-1705
Number of pages6
JournalAnalytical Chemistry
Volume69
Issue number9
DOIs
Publication statusPublished - May 1 1997

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Enantiomers
Alkalinity
Phenylalanine
Dimers
Amino Acids
Proline
Gases
Ions
Stereochemistry
Valine
Tryptophan
Kinetic energy
Alanine
Mass spectrometry
Kinetics

ASJC Scopus subject areas

  • Analytical Chemistry

Cite this

Distinction of amino acid enantiomers based on the basicity of their dimers. / Vékey, K.; Czira, Gábor.

In: Analytical Chemistry, Vol. 69, No. 9, 01.05.1997, p. 1700-1705.

Research output: Contribution to journalArticle

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