Characterization of protonated phospholipids as fragile ions in quadrupole ion trap mass spectrometry

Abstract

Some ions exhibit “ion fragility” in quadrupole ion trap mass spectrometry (QIT-MS) during mass analysis with resonance ejection. In many cases, different ions generated from the same compound exhibit different degrees of ion fragility, with some ions (e.g., the [M+H] + ion) stable and other ions (e.g., the [M+Na] + ion) fragile. The ion fragility for quadrupole ion trap (QIT) mass spectrometry (MS) for protonated and sodiated ions of three phospholipids, 1,2-dipalmitoyl- sn-glycero-3-phosphocholine, PC (16:0/16:0), 1,2-dipalmitoyl- sn-glycero-3-phophoethanolamine, PE (16:0/16:0), and N-palmitoyl- d- erythro-sphingosylphosphorylcholine, SM (d18:1/16:0), was determined using three previously developed experiments: (1) the peak width using a slow scan speed, (2) the width of the isolation window for efficient isolation, and (3) the energy required for collision-induced dissociation. In addition, ion fragility studies were designed and performed to explore a correlation between ion fragility in QIT mass analysis and ion fragility during transport between the ion source and the ion trap. These experiments were: (1) evaluating the amount of thermal-induced dissociation as a function of heated capillary temperature, and (2) determining the extent of fragmentation occurring with increasing tube lens voltage. All phospholipid species studied exhibited greater ion fragility as protonated species in ion trap mass analysis than as sodiated species. In addition, the protonated species of both SM (d18:0/16:0) and PC (16:0/16:0) exhibited greater tendencies to fragment at higher heated capillary temperatures and high tube lens voltages, whereas the PE (16:0/16:0) ions did not appear to exhibit fragility during ion transport.