AI Article Synopsis

  • Hydrogen/deuterium exchange (HDX) mass spectrometry (MS) is often used for analyzing protein structures, particularly in biopharmaceutical development.
  • The method can reveal distinct patterns in proton exchange, which helps understand protein behavior in solution, but it’s crucial to ensure these patterns are not just artifacts from the analysis.
  • The study identifies a new source of artificial bimodal isotope patterns in highly charged peptides, caused by gas-phase proton exchanges, and suggests minor adjustments in ion guide settings to eliminate this issue without losing signal quality.

Article Abstract

Hydrogen/deuterium exchange (HDX) mass spectrometry (MS) for protein structural analysis has been adopted for many purposes, including biopharmaceutical development. One of the benefits of examining amide proton exchange by mass spectrometry is that it can readily resolve different exchange regimes, as evidenced by either binomial or bimodal isotope patterns. By careful analysis of the isotope pattern during exchange, more insight can be obtained on protein behavior in solution. However, one must be sure that any observed bimodal isotope patterns are not artifacts of analysis and are reflective of the true behavior in solution. Sample carryover and certain stationary phases are known as potential sources of bimodal artifacts. Here, we describe an additional undocumented source of deuterium loss resulting in artificial bimodal patterns for certain highly charged peptides. We demonstrate that this phenomenon is predominantly due to gas-phase proton exchange between peptides and bulk solvent within the initial stages of high-transmission conjoined ion guides. Minor adjustments of the ion guide settings, as reported here, eliminate the phenomenon without sacrificing signal intensity. Such gas-phase deuterium loss should be appreciated for all HDX-MS studies using such ion optics, even for routine studies not focused on interpreting bimodal spectra. Graphical Abstract ᅟ.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4829384PMC
http://dx.doi.org/10.1007/s13361-015-1330-8DOI Listing

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