Mass spectrometry-based methods for detection and differentiation of botulinum neurotoxins
AssigneeLos Alamos National Security, LLC
InventorsJurgen G. Schmidt, Anne E. Boyer, Suzanne R. Kalb, Hercules Moura, John R. Barr, Adrian R. Woolfitt
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Abstract
The present invention is directed to a method for detecting the presence of clostridial neurotoxins in a sample by mixing a sample with a peptide that can serve as a substrate for proteolytic activity of a clostridial neurotoxin; and measuring for proteolytic activity of a clostridial neurotoxin by a mass spectroscopy technique. In one embodiment, the peptide can have an affinity tag attached at two or more sites.
Claims13
A method for detecting the presence of clostridial botulinum neurotoxins in a sample comprising the steps of:
- a) mixing a sample that may comprise serotypes of clostridial neurotoxins with a peptide substrate, wherein said peptide substrate is KGSNRTRIDEANORATRMLGGK-(SEQ ID NO:
- 1), and optionally, one or more peptide substrates selected from the group consisting of SEQ ID NO:14, 21, and 28, for proteolytic activity of said clostridial neurotoxin serotypes, such that at least a portion of the amount of the substrate is proteolytically cleaved by a serotype to produce a mixture comprising uncleaved substrate and peptide cleavage products;
- b) analyzing the mixture on a mass spectrometer to produce a signal corresponding to the mass of at least one peptide cleavage product;
- c) using the signal corresponding to the peptide cleavage products to identify the clostridial neurotoxin serotype;
- d) quantitating the amount of proteolytic cleavage of the peptide substrate for the clostridial neurotoxin serotype by stable isotope dilution mass spectrometry.
Dependencies are inferred from the claim text.