Liquid Chromatography-Electrospray Ionization Mass Spectrometry of 4-(3-Pyridinylmethylaminocarboxypropyl) phenylthiohydantoins

• Published in: Analytical biochemistry Vol. 224; no. 1; pp. 373 - 381
• Main Authors: Hess, D., Nika, H., Chow, D.T., Bures, E.J., Morrison, H.D., Aebersold, R.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 1995
• Subjects: Amino Acid Sequence; Chromatography, High Pressure Liquid; Hydantoins - analysis; Mass Spectrometry; Molecular Sequence Data; Sensitivity and Specificity
• ISSN: 0003-2697; 1096-0309
• DOI: 10.1006/abio.1995.1053

We report the separation of 4-(3-pyridinylmethylaminocarboxypropyl) phenylthiohydantoins by microbore reverse-phase high-performance liquid chromatography and their detection by on-line electrospray ionization mass spectrometry. These compounds are the products of the chemical stepwise degradation of polypeptides using 4-(3-pyridinylmethylaminocarboxypropyl) phenyl isothiocyanate. We describe chromatographic conditions for on-column concentration of the analytes and for baseline separation of the isobaric amino acid derivatives of leucine and isoleucine. A commercially available protein sequencer was readily interfaced with the described analytical system and used for adsorptive sequence analysis of a panel of synthetic peptides containing collectively all 20 naturally occurring amino acids. On-line mass analysis of derivatives generated by automated sequencing confirmed that the derivatives were of the predicted mass and were detectable at comparable signal strength and sensitivity. Finally, we demonstrate that the additional selectivity in data interpretation provided by mass analysis dramatically improves the signal-to-noise ratio and therefore enhances the ability to conclusively interpret protein and peptide sequence data.