# Proton transfer reagent cations for ion–ion charge state manipulation of high mass negatively-charged analytes in an electrodynamic ion trap

**Authors:** Nicholas R. Ellin, Boukar K. S. Faye, Seth A. Horn, Alexander M. Koers, Scott A. McLuckey

PMC · DOI: 10.1039/d5an01354b · The Analyst · 2026-02-18

## TL;DR

This paper explores how to use proton transfer reagents to manipulate the charge of large negatively-charged molecules in an ion trap for better analysis.

## Contribution

The study introduces PFDA as a new reagent for efficient and selective proton transfer in ion traps.

## Key findings

- Protonated PFDA is effective for proton transfer to high mass multiply-charged analytes.
- PFDA shows less ion attachment compared to proton sponge in ion/ion reactions.
- Mild collisional heating can remove PFDA adducts from oligonucleotides.

## Abstract

This work summarizes the criteria for a useful reagent for ion/ion proton transfer in an electrodynamic ion trap with specific emphasis on proton transfer to high mass multiply-charged analyte ions. A readily available and ionizable weak base of relatively high mass meets the criteria. The protonated form of an extensively fluorinated 10-carbon primary amine (1H,1H,2H,2H-perfluorodecylamine, PFDA) is demonstrated to serve as a useful reagent for proton transfer to negatively-charged proteins and oligonucleotides. The behavior of protonated PFDA is compared with that of protonated 1,8-bis(dimethylamino)naphthalene (proton sponge) with respect to the tendency for proton transfer versus attachment in ion/ion reactions with a common multiply-deprotonated protein and a common multiply-deprotonated oligonucleotide. Protonated PFDA showed a lesser tendency for ion attachment than the proton sponge in all cases. Both reagent cations showed a greater extent of attachment to the oligonucleotide anions. Mild collisional heating was shown to be able to extensively remove adducted PFDA from the oligonucleotide. The ability to generate low z and high m/z analyte product ions from highly charged precursor analyte ions using protonated PDFA is illustrated with anions derived from β-galactosidase, GroEL, and 30S E. coli ribosome particles.

This work summarizes the criteria for a useful reagent for ion/ion proton transfer in an electrodynamic ion trap with specific emphasis on proton transfer to high mass multiply-charged analyte ions.

## Linked entities

- **Proteins:** HSPD1 (heat shock protein family D (Hsp60) member 1)
- **Chemicals:** 1H,1H,2H,2H-perfluorodecylamine (PubChem CID 2783341), 1,8-bis(dimethylamino)naphthalene (PubChem CID 88675), PFDA (PubChem CID 9555)

## Full-text entities

- **Chemicals:** 1,8-bis(dimethylamino)naphthalene (MESH:C418992), oligonucleotide (MESH:D009841), 10-carbon primary amine (-)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12935111/full.md

## References

93 references — full list in the complete paper: https://tomesphere.com/paper/PMC12935111/full.md

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Source: https://tomesphere.com/paper/PMC12935111