All-ions laser induced dissociation (AI-LID) in the C-trap of a Q Exactive: Data independent identification and quantification directly from ultra-high resolution differential mass spectra

An analytical method is demonstrated which allows to follow a data independent, all ion fragmentation (AIF) acquisition procedure, but to fall back on a standard and generic data-dependent acquisition (DDA) analysis procedure for the data treatment: searching databases with individual precursor ions and fragments lists. This method is implemented with photo-activation (LID) in the visible range which allows extreme specificity and sensitivity, and is demonstrated on Cysteine-containing tryptic peptides grafted with a chromophore. This proof of concept relies on the efficient implementation of LID directly in the C-trap of a ThermoScientific QExactive mass spectrometer during ion accumulation, before full MS detection. Laser irradiation turned alternatively ON and OFF after each full MS allows to build differential mass spectra in which non-dissociating ions are cancelled out while fragmenting precursors and fragments show up with opposite signs, which enables to build precursor/fragments lists for database search. Protein identification was demonstrated with remarkably low false discovery rates. Relative quantification was also demonstrated by integration of precursor and fragment ion elution peaks after differential analysis and limits of quantifications were demonstrated down to 11 ng of proteins injected. This mixed approach takes the best of both worlds – the deep proteome coverage of DIA, with the exhaustive fragmentation of all precursor ions, and the reliability and ease of use of classical DDA database search, relieving the need for the initial constitution of a spectral library. • LID fragmentation of chromophore derivatized cysteine-containing peptides in the C-Trap of an orbitrap-based mass spectrometer • New acquisition sequence which consists in recording full MS at max resolution alternatively with and without laser irradiation. • Differential analysis allowing simultaneous generation of precursors and fragments lists for automated theoretical database search and protein identification with nearly no FDR • Extraction of specific precursor and fragment ion chromatograms from differential datasets for sensitive relative quantification with a high degree of confidence.

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Journal
International Journal of Mass Spectrometry
Published
2025-06-18
DOI
https://doi.org/10.1016/j.ijms.2025.117484
Primary Topic
Mass Spectrometry Techniques and Applications
Type
article
Field-Weighted Citation Impact
0.00

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article

All-ions laser induced dissociation (AI-LID) in the C-trap of a Q Exactive: Data independent identification and quantification directly from ultra-high resolution differential mass spectra

Marion Girod, Jérôme Lemoine, Lény Garcia, Philippe Dugourd et al.
International Journal of Mass Spectrometry
Mass Spectrometry Techniques and Applications
article

All-ions laser induced dissociation (AI-LID) in the C-trap of a Q Exactive: Data independent identification and quantification directly from ultra-high resolution differential mass spectra

Marion Girod, Jérôme Lemoine, Lény Garcia, Philippe Dugourd, Luke MacAleese, Xavier Dagany
article en

Abstract

An analytical method is demonstrated which allows to follow a data independent, all ion fragmentation (AIF) acquisition procedure, but to fall back on a standard and generic data-dependent acquisition (DDA) analysis procedure for the data treatment: searching databases with individual precursor ions and fragments lists. This method is implemented with photo-activation (LID) in the visible range which allows extreme specificity and sensitivity, and is demonstrated on Cysteine-containing tryptic peptides grafted with a chromophore. This proof of concept relies on the efficient implementation of LID directly in the C-trap of a ThermoScientific QExactive mass spectrometer during ion accumulation, before full MS detection. Laser irradiation turned alternatively ON and OFF after each full MS allows to build differential mass spectra in which non-dissociating ions are cancelled out while fragmenting precursors and fragments show up with opposite signs, which enables to build precursor/fragments lists for database search. Protein identification was demonstrated with remarkably low false discovery rates. Relative quantification was also demonstrated by integration of precursor and fragment ion elution peaks after differential analysis and limits of quantifications were demonstrated down to 11 ng of proteins injected. This mixed approach takes the best of both worlds – the deep proteome coverage of DIA, with the exhaustive fragmentation of all precursor ions, and the reliability and ease of use of classical DDA database search, relieving the need for the initial constitution of a spectral library. • LID fragmentation of chromophore derivatized cysteine-containing peptides in the C-Trap of an orbitrap-based mass spectrometer • New acquisition sequence which consists in recording full MS at max resolution alternatively with and without laser irradiation. • Differential analysis allowing simultaneous generation of precursors and fragments lists for automated theoretical database search and protein identification with nearly no FDR • Extraction of specific precursor and fragment ion chromatograms from differential datasets for sensitive relative quantification with a high degree of confidence.

International Journal of Mass SpectrometryVol. 515
Université Claude Bernard Lyon 1 (FR), Centre National de la Recherche Scientifique (FR), Institut des Sciences Analytiques (FR), Institut Lumière Matière (FR)
European Commission
Climate action
Openalex Percentile: Top 87%
Mass Spectrometry Techniques and Applications
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