Abstract
Electrospray
ionization (ESI) in-source fragmentation (ISF) has traditionally been
minimized to promote precursor molecular ion formation, and therefore its value
in molecular identification underappreciated. Recently a METLIN-guided
in-source annotation (MISA) algorithm was introduced to increase confidence in putative
identifications by using ubiquitous in-source fragments. However, MISA is
limited by ESI sources that are generally designed to minimize ISF. In this
study, enhanced ISF with MISA (eMISA) was created by tuning the ISF conditions
to generate in-source fragmentation patterns comparable with higher energy
fragments generated at higher collision energies as deposited in the METLIN
MS/MS library, without compromising the intensity of precursor ions (median
loss ≤ 10% in both positive and negative ionization modes). The analysis of 50
molecules was used to validate the approach in comparison to MS/MS spectra
produced via data dependent acquisition (DDA) and data independent acquisition
mode (DIA) with quadrupole time-of-flight mass spectrometry (QTOF-MS). Enhanced
ISF as compared to QTOF DDA, enables for higher peak intensities for the
precursor ions (median: 18 times at negative mode and 210 times at positive
mode), with the eMISA fragmentation patterns consistent with METLIN for over 90%
of the molecules with respect to fragment relative intensity and m/z.
eMISA also provides higher peak intensity as opposed to QTOF DIA with a median
increase of 20% at negative mode and 80% at positive mode for all precursor
ions. Metabolite identification with eMISA was also successfully validated from
the analysis of a metabolic extract from macrophages. An interesting side
benefit of enhanced ISF is that it significantly improved the compound
identification confidence with low resolution single quadrupole mass
spectrometry-based untargeted LC/MS experiments. Overall, enhanced ISF allowed
for eMISA to be used as a more sensitive alternative to other QTOF DIA and DDA
approaches, and further, it enables the acquisition of ESI TOF and ESI single
quadrupole mass spectrometry instrumentation spectra with higher sensitivity
and improved molecular identification confidence.