Top-Down Characterization of Bacterial Lipopolysaccharides and Lipooligosaccharides Using Activated-Electron Photodetachment Mass Spectrometry.
James E KeenerByoungsook GohJi-Sun YooSungwhan F OhJennifer S BrodbeltPublished in: Analytical chemistry (2024)
Lipopolysaccharides (LPS) and lipooligosaccharides (LOS) are located in the outer membrane of Gram-negative bacteria and are comprised of three distinctive parts: lipid A, core oligosaccharide (OS), and O-antigen. The structure of each region influences bacterial stability, toxicity, and pathogenesis. Here, we highlight the use of targeted activated-electron photodetachment (a-EPD) tandem mass spectrometry to characterize LPS and LOS from two crucial players in the human gut microbiota, Escherichia coli Nissle and Bacteroides fragilis . a-EPD is a hybrid activation method that uses ultraviolet photoirradiation to generate charge-reduced radical ions followed by collisional activation to produce informative fragmentation patterns. We benchmark the a-EPD method for top-down characterization of triacyl LOS from E. coli R2, then focus on characterization of LPS from E. coli Nissle and B. fragilis . Notably, a-EPD affords extensive fragmentation throughout the backbone of the core OS and O-antigen regions of LPS from E. coli Nissle. This hybrid approach facilitated the elucidation of structural details for LPS from B. fragilis , revealing a putative hexuronic acid (HexA) conjugated to lipid A.
Keyphrases
- escherichia coli
- inflammatory response
- anti inflammatory
- tandem mass spectrometry
- liquid chromatography
- mass spectrometry
- high performance liquid chromatography
- gas chromatography
- ultra high performance liquid chromatography
- simultaneous determination
- high resolution
- fatty acid
- solid phase extraction
- oxidative stress
- photodynamic therapy
- quantum dots
- drug delivery
- biofilm formation
- high resolution mass spectrometry
- pluripotent stem cells
- staphylococcus aureus
- cystic fibrosis
- capillary electrophoresis
- water soluble