Identification of unusual amino acids in peptides using automated sequential Edman degradation coupled to direct detection by electrospray-ionization mass spectrometry

The determination of the primary structure of peptides and proteins is routine in many laboratories; however, many of the obtained sequences are incomplete or can be misinterpreted when the samples contain unusual amino acids. Here we report the development of an automated peptide sequenator coupled to an electrospray‐ionization (ESI) mass spectrometer (MS) that, in conjunction with minor modifications to the sequencing conditions and, in some cases, prior derivatization of amino acids, allows the detection of the phenylthiohydantoin (PTH) derivatives of a number of unusual amino acids. Using the coupled sequenator–ESI–MS system we were able to determine the complete sequence of the lantibiotic gallidermin, a partial sequence of the calcium‐dependent peptide antibiotic CDA2 as well as the pool sequence of a mixture of synthetic peptides containing nonproteinogenic amino acids. In addition to the 20 proteinogenic amino acids, the procedure was able to detect PTH derivatives of hydroxyphenylglycine (Hpg), 2,3‐didehydroasparagine, 3‐methylglutamic acid (MeGlu), oxytryptophan, ornithine (Orn), N‐methylglycine (Nmg), dihydroxyphenylalanine (DOPA), and α‐aminoisobutyric acid (Aib). Similarly, after a simple derivatization procedure, we were also able to correctly identify educts of 2,3‐didehydroalanine (Dha), 2,3‐didehydrobutyrine (Dhb), lanthionine (Lan), and 3‐methyllanthionine (MeLan). © 1999 John Wiley & Sons, Inc. Biopoly 49: 329–340, 1999