Peptide separation selectivity in proteomics LC‐MS experiments: Comparison of formic and mixed formic/heptafluorobutyric acids ion‐pairing modifiers
Daniel Gussakovsky, Geoff Anderson, Vic Spicer, Oleg V. Krokhin
Abstract
Abstract Separation selectivity and detection sensitivity of reversed‐phase high‐performance liquid chromatography with tandem mass spectrometry analyses were compared for formic (0.1%) and formic/heptafluorobutyric (0.1%/0.005%) acid based eluents using a proteomic data set of ∼12 000 paired peptides. The addition of a small amount of hydrophobic heptafluorobutyric acid ion‐pairing modifier increased peptide retention by up to 10% acetonitrile depending on peptide charge, size, and hydrophobicity. Retention increase was greatest for peptides that were short, highly charged, and hydrophilic. There was an ∼3.75‐fold reduction in MS signal observed across the whole population of peptides following the addition of heptafluorobutyric acid. This resulted in ∼36% and ∼21% reduction of detected proteins and unique peptides for the whole cell lysate digests, respectively. We also confirmed that the separation selectivity of the formic/heptafluorobutyric acid system was very similar to the commonly used conditions of 0.1% trifluoroacetic acid, and developed a new version of the Sequence‐Specific Retention calculator model for the formic/heptafluorobutyric acid system showing the same ∼0.98 R 2 ‐value accuracy as the Sequence‐Specific Retention calculator formic acid model. In silico simulation of peptide distribution in separation space showed that the addition of 0.005% heptafluorobutyric acid to the 0.1% formic acid system increased potential proteome coverage by ∼11% of detectable species (tryptic peptides ≥ four amino acids).