Identification and quantification of the enantiomeric excess of O-phosphoserine (OPSer) residues from post-translational modified proteins is now possible by the application of a very reproducible and sensitive mass spectrometric method. This technique is based on the different mass-spectral fragmentation patterns of the diastereomeric cluster ions generated in water/methanol solutions of the analyte (OPSerD/L) with a suitable chiral compound (OPThrL) by collision-induced dissociation (CID; see mass spectra).
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Fago et al. (2001) studied this question.
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