Analysis of tryptic peptides using desorption electrospray ionisation combined with ion mobility spectrometry/mass spectrometry

• Published in: Rapid communications in mass spectrometry Vol. 21; no. 7; pp. 1131 - 1138
• Main Authors: Kaur-Atwal, Gushinder, Weston, Daniel J., Green, Philip S., Crosland, Susan, Bonner, Philip L. R., Creaser, Colin S.
• Format: Journal Article
• Language: English
• Published: Chichester, UK John Wiley & Sons, Ltd 01.01.2007
• Subjects: Amino Acid Sequence; Molecular Sequence Data; Peptide Mapping - methods; Peptides - chemistry; Sequence Analysis, Protein - methods; Spectrometry, Mass, Electrospray Ionization - methods
• ISSN: 0951-4198; 1097-0231
• DOI: 10.1002/rcm.2941

A novel method is reported for rapid protein identification by the analysis of tryptic peptides using desorption electrospray ionisation (DESI) coupled with hyphenated ion mobility spectrometry and quadrupole time‐of‐flight mass spectrometry (IMS/Q‐ToF‐MS). Confident protein identification is demonstrated for the analysis of tryptically digested bovine serum albumin (BSA), with no sample pre‐treatment or clean‐up. Electrophoretic ion mobility separation of ions generated by DESI allowed examination of charge‐state and mobility distributions for tryptic peptide mixtures. Selective interrogation of singly charged ions allowed isobaric peptide responses to be distinguished, along with a reduction in spectral noise. The mobility‐selected singly charged peptide responses were presented as a pseudo‐peptide mass fingerprint (p‐PMF) for protein database searching. Comparative data are shown for electrospray ionisation (ESI) of the BSA digest, without sample clean‐up, from which confident protein identification could not be made. Implications for the robustness of the DESI method, together with potential insights into mechanisms for DESI of proteolytic digests, are discussed. Copyright © 2007 John Wiley & Sons, Ltd.