Improved Performance of Positive-Ion Mode Free Radical-Initiated Peptide Sequencing with p -TEMPO-Bz.

Autor: Osho KE; Department of Chemistry, University of Nevada, 1664 North Virginia Street, Reno, Nevada 89557, United States., Wasik KA; Department of Chemistry, University of Nevada, 1664 North Virginia Street, Reno, Nevada 89557, United States., Geary LM; Department of Chemistry, University of Nevada, 1664 North Virginia Street, Reno, Nevada 89557, United States., Borotto NB; Department of Chemistry, University of Nevada, 1664 North Virginia Street, Reno, Nevada 89557, United States.
Jazyk: angličtina
Zdroj: Journal of the American Society for Mass Spectrometry [J Am Soc Mass Spectrom] 2023 Apr 05; Vol. 34 (4), pp. 579-585. Date of Electronic Publication: 2023 Feb 23.
DOI: 10.1021/jasms.2c00306
Abstrakt: Free radical-initiated peptide sequencing (FRIPS) is a tandem mass spectrometry technique that generates sequence informative ions via collisionally initiated radical chemistry. Collision activation homolytically cleaves an installed radical precursor and initiates radical formation, extensive hydrogen atom transfer, and peptide backbone dissociation. While the FRIPS technique shows great promise, when applied to multiply charged derivatized peptide ions, a series of high-abundance mass losses are observed which siphon ion abundance from radically generated sequence ions. This loss of ion abundance reduces the sequence coverage generated by FRIPS fragmentation. In this work, we hypothesized that these mass losses were assisted by the ortho -orientation of the radical precursor undergoing facile conversion into five- or six-membered intermediates or products and that when combined with the lower bond dissociation energy of the para -precursor, conjugated peptides would not undergo this chemistry. To test this assertion, we synthesized p -TEMPO-Bz, conjugated it to these peptides, and collisionally activated each. Indeed, we see dramatic attenuation of these undesired collisional processes and a significant increase in radical precursor ion abundance. The increase in ion abundance leads to a significant increase in the sequence coverage generated. These results demonstrate that p -TEMPO-Bz significantly improves the performance of positive-ion mode FRIPS and may be a compelling alternative to the currently utilized o -TEMPO-Bz-based FRIPS.
Databáze: MEDLINE