| Literature DB >> 21205003 |
Hercules Moura1, Rebecca R Terilli, Adrian R Woolfitt, Maribel Gallegos-Candela, Lisa G McWilliams, Maria I Solano, James L Pirkle, John R Barr.
Abstract
Botulinum neurotoxins (BoNTs) are very potent toxins and category A biological threat agents. BoNT serotypes /C1 and /D affect birds and mammals and can be potentially lethal to humans. We have previously described the usefulness of the Endopep-MS method to detect the activity of BoNT A through G. This report was followed by the application of the method to clinical samples. The activity of the BoNT serotypes associated with human disease (/A, /B, /E, and /F) was successfully detected. However, BoNT/C and /D require different conditions for fast substrate cleavage, and a comprehensive description of a method to study BoNT/C and /D has not yet been reported. This work describes a new, optimized version of the Endopep-MS method to detect BoNTs /C1 and /DC either spiked directly in 20 μL of reaction buffer or spiked in a larger volume of buffer and further extracted using antibody-coated magnetic beads. It was found that the incubation temperature at 42 °C was more effective for both toxin serotypes, but each toxin serotype has an optimum cleavage pH. Additionally, we describe for the first time a proteomics study using a fast trypsin digestion method and label-free quantification of these toxin serotypes. FEMS Immunology & Medical MicrobiologyEntities:
Mesh:
Substances:
Year: 2011 PMID: 21205003 DOI: 10.1111/j.1574-695X.2010.00774.x
Source DB: PubMed Journal: FEMS Immunol Med Microbiol ISSN: 0928-8244