Publication | Closed Access
From the Mouse to the Mass Spectrometer: Detection and Differentiation of the Endoproteinase Activities of Botulinum Neurotoxins A−G by Mass Spectrometry
144
Citations
14
References
2005
Year
ToxinologyBont TypeImmunologyBiological Mass SpectrometryEndoproteinase ActivitiesBotulinum Neurotoxins A−gProteomic TechnologyBioanalysisAnalytical ChemistryAnalytical BiotechnologyProteomicsBiochemistryBont TypesNatural SciencesPeptide LibraryMass SpectrometryProtein Mass SpectrometryMicrobiologyMedicine
We have developed an assay (Endopep-MS) that detects the specific endoproteinase activities of all seven BoNT types by mass spectrometry (MS). Each BoNT type cleaves a unique site on proteins involved in neuronal transmission. Target peptide substrates based on these proteins identify a BoNT type by its enzymatic action on the substrate and the production of two peptide products, which are then detected by matrix-assisted laser desorption/ionization time-of-flight MS or liquid chromatography electrospray ionization MS/MS. We showed the ability to detect all seven toxin types in a multiplexed assay format. The detection limits achieved range from 0.039 to 0.625 mouse LD(50)/mL for toxin types A, B, E, and F in a buffer system. The Endopep-MS assay is the first to differentiate all seven BoNT types, is sensitive, specific, and has the potential to quantify toxin activity.
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