Localization of Post-Translational Modifications in Peptide Mixtures via High-Resolution Differential Ion Mobility Separations Followed by Electron Transfer Dissociation

J Am Soc Mass Spectrom. 2016 Dec;27(12):2064-2070. doi: 10.1007/s13361-016-1498-6. Epub 2016 Sep 19.

Abstract

Precise localization of post-translational modifications (PTMs) on proteins and peptides is an outstanding challenge in proteomics. While electron transfer dissociation (ETD) has dramatically advanced PTM analyses, mixtures of localization variants that commonly coexist in cells often require prior separation. Although differential or field asymmetric waveform ion mobility spectrometry (FAIMS) achieves broad variant resolution, the need for standards to identify the features has limited the utility of approach. Here we demonstrate full a priori characterization of variant mixtures by high-resolution FAIMS coupled to ETD and the procedures to systematically extract the FAIMS spectra for all variants from such data. Graphical Abstract ᅟ.

Keywords: Electron transfer dissociation; FAIMS; Ion mobility spectrometry; PTM localization.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Electrons
  • Ion Mobility Spectrometry*
  • Peptides / metabolism*
  • Pilot Projects
  • Protein Processing, Post-Translational*
  • Proteins
  • Proteomics

Substances

  • Peptides
  • Proteins