Rapid Quantification of Clostridial Epsilon Toxin in Complex Food and Biological Matrixes by Immunopurification and Ultraperformance Liquid Chromatography-Tandem Mass Spectrometry
journal contributionposted on 05.06.2012, 00:00 by Alexandre Seyer, François Fenaille, Cecile Féraudet-Tarisse, Hervé Volland, Michel R. Popoff, Jean-Claude Tabet, Christophe Junot, François Becher
Epsilon toxin (ETX) is one of the most lethal toxins produced by Clostridium species and is considered as a potential bioterrorist weapon. Here, we present a rapid mass spectrometry-based method for ETX quantification in complex matrixes. As a prerequisite, naturally occurring prototoxin and toxin species were first structurally characterized by top-down and bottom-up experiments, to identify the most pertinent peptides for quantification. Following selective ETX immunoextraction and trypsin digestion, two proteotypic peptides shared by all the toxin forms were separated by ultraperformance liquid chromatography (UPLC) and monitored by ESI-MS (electrospray ionization-mass spectrometry) operating in the multiple reaction monitoring mode (MRM) with collision-induced dissociation. Thorough protocol optimization, i.e., a 15 min immunocapture, a 2 h enzymatic digestion, and an UPLC-MS/MS detection, allowed the whole quantification process including the calibration curve to be performed in less than 4 h, without compromising assay robustness and sensitivity. The assay sensitivity in milk and serum was estimated at 5 ng·mL–1 for ETX, making this approach complementary to enzyme linked immunosorbent assay (ELISA) techniques.
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Complex Foodtoxin speciesreaction monitoring mode2 hMRM4 hassay sensitivityClostridium species15 min immunocaptureassay robustnessUPLCETX immunoextractionproteotypic peptidesClostridial Epsilon Toxinquantification processimmunosorbent assayBiological MatrixesELISAETX quantificationbioterrorist weapontrypsin digestionThorough protocol optimizationRapid Quantificationtoxin formscalibration curve