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Chiral Analysis by Electrospray Ionization Mass Spectrometry/Mass Spectrometry. 2. Determination of Enantiomeric Excess of Amino Acids
Ist Teil von
Analytical chemistry (Washington), 2000-11, Vol.72 (21), p.5394-5401
Ort / Verlag
Washington, DC: American Chemical Society
Erscheinungsjahr
2000
Link zum Volltext
Quelle
MEDLINE
Beschreibungen/Notizen
The determination of enantiomeric excess (ee) of amino acids was achieved by investigating the collision-induced dissociation spectra of protonated trimers that were formed by electrospray ionization of amino acids in the presence of one of the following chiral selectors: l- or d-N -tert-butoxycarbonylphenylalanine, l- or d- N-tert-butoxycarbonylproline, and l- or d-N-tert- butoxycarbonyl-O-benzylserine. The protonated trimers were dissociated to form protonated dimers, and the observed dissociation efficiency r (i.e., the intensity ratio of protonated dimers to protonated trimers) for an enantiomeric mixture was found to be related to its ee value by the following equation: r = a + b/(c + ee), where a, b, and c were constants. A linear calibration plot was obtained by plotting r versus 1/(c + ee), where c was calculated with the MATLAB software, or by plotting 1/(r − r 0) versus 1/ee, where r 0 was the r value for the racemic mixture. The latter “two-reciprocal” method was more convenient for application. Another practical method for ee determination was the “three-point” method, whereby the ee of an unknown sample with a measured r value could be derived from the equation ee = 100{1/(r L − r 0) − 1/(r D − r 0)}/{2/(r − r 0) − 1/(r L − r 0) − 1/(r D − r 0)}, with r L and r D being the r values for the enantiomerically pure l- and d-forms of the sample, respectively. A calibration plot was not required. The ee determination was achieved with acceptable precision even for the worst case of acceptable chiral recognition with a particular chiral selector, suggesting that the ee determination of all 19 common amino acids could be achieved by the present method. The ee of a histidine sample was determined both by the two-reciprocal method, giving an error of 0.2% ee (1.1% relative error) and consuming only ∼5.3 nmol of sample, and by the three-point method, giving an error of 0.4% ee and consuming only ∼2.3 nmol of sample. In the latter case, it took 27 min for the mass spectrometric measurements of the three calibration standards and an additional 9 min for the unknown sample. The direct ee determination of more than one amino acid in a mixture was also demonstrated in the study.