From the mouse to the mass spectrometer: detection and differentiation of the endoproteinase activities of botulinum neurotoxins A− G by mass spectrometry

AE Boyer, H Moura, AR Woolfitt, SR Kalb… - Analytical …, 2005 - ACS Publications
AE Boyer, H Moura, AR Woolfitt, SR Kalb, LG McWilliams, A Pavlopoulos, JG Schmidt…
Analytical chemistry, 2005ACS Publications
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 …
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 LD50/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.
ACS Publications
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