Rapid MALDI-MS/MS-Based Profiling of Lipid A Species from Gram-Negative Bacteria Utilizing Trapped Ion Mobility Spectrometry and mzmine
Lipid A, a crucial component of lipopolysaccharides (LPS), plays a pivotal role in the pathogenesis of Gram-negative bacteria. Lipid A patterns are recognized by mammals and can induce immunostimulatory effects. However, the outcome of the interaction is highly dependent on the chemical composition of individual lipid A species. The diversity of potential fatty acyl and polar headgroup combinations in this complex saccharolipid presents a significant analytical challenge. Current mass spectrometry (MS)-based lipid A methods are focused on either direct matrix-assisted laser desorption/ionization (MALDI)-MS screening or comprehensive structural elucidation by tandem mass spectrometry (MS/MS) hyphenated with separation techniques. In this study, we developed an alternative workflow for rapid lipid A profiling covering the entire analysis pipeline from sample preparation to data analysis. This workflow is based on microextraction and subsequent MALDI-MS/MS analysis of uropathogenic <i>Escherichia coli</i> utilizing trapped ion mobility spectrometry (TIMS), followed by mzmine data processing. The additional TIMS dimension served for enhanced sensitivity, selectivity, and structural elucidation through mobility-resolved fragmentation via parallel accumulation-serial fragmentation (PASEF) in parallel reaction monitoring (prm)-mode. Furthermore, mzmine enabled automated MS/MS acquisition by adapting the spatial ion mobility-scheduled exhaustive fragmentation (SIMSEF) strategy for MALDI spot analysis. It also facilitated robust lipid A annotation through a newly developed extension of the rule-based lipid annotation module, allowing for the custom generation of lipid classes, including specific fragmentation rules. In this study, the first publication of lipid A species' collision cross section (CCS) values is reported, which will enhance high-confidence lipid A annotation in future studies.
Authors
- Matti Froning (ORCID: https://orcid.org/0000-0003-3097-4116)
- Edward Rudt (ORCID: https://orcid.org/0000-0003-4351-3212)
- Ansgar Korf (ORCID: https://orcid.org/0000-0002-2769-2460)
- Robin Schmid (ORCID: https://orcid.org/0000-0003-0922-3887)
- Ulrich Dobrindt (ORCID: https://orcid.org/0000-0001-9949-1898)
- Heiko Hayen (ORCID: https://orcid.org/0000-0002-4074-8545)
- Steffen Heuckeroth (ORCID: https://orcid.org/0000-0002-4928-2526)
- Tomáš Pluskal (ORCID: https://orcid.org/0000-0002-6940-3006)
- Lucas Ortmann (ORCID: https://orcid.org/0009-0002-4929-2078)
- Julia Diemand
- Linus Hörnschemeyer
- Alexander Pleger
- Max Vinzelberg
Institutions
- University of Bremen (DE)
- University of Münster (DE)
- Czech Academy of Sciences, Institute of Organic Chemistry and Biochemistry (CZ)
Publication Details
- Journal
- Analytical Chemistry
- Published
- 2025-04-01
- DOI
- https://doi.org/10.1021/acs.analchem.4c05989
- Citations
- 4
- Primary Topic
- Metabolomics and Mass Spectrometry Studies
- Type
- article
- Field-Weighted Citation Impact
- 3.22