High-Throughput Assays for Botulinum Neurotoxin Proteolytic Activity: Serotypes A, B, D, and F Export

@article{citeulike:2760314, abstract = {Botulinum neurotoxins (BoNT) are zinc metalloproteases that cleave and inactivate cellular proteins essential for neurotransmitter release. Because the paralytic effect of BoNT is a consequence of its enzymatic activity, selective inhibitors may be useful as drugs or as tools for further research. To expedite inhibitor discovery, we developed high-throughput, solid-phase protease activity assays for four of the seven BoNT serotypes: A, B, D, and F. Each assay consisted of a cleavable oligopeptide, based on the natural substrate sequence, labeled with fluorescein and covalently attached to maleimide-activated multiwell plates. Solutions of holotoxin or nontoxic catalytic domain of BoNT were incubated in substrate-coated wells, with or without test compounds, followed by transfer and assay of solubilized product in a multiwell fluorometer. Routine toxin concentrations ranged from 10 to 100 ng/ml, but concentrations as low as 2 ng/ml gave reproducible signals. The fluorescence assays were selective, gave very low background readings, and were stable upon prolonged storage. Using the nontoxic catalytic domain of BoNT A, we determined the relative inhibitory potencies of a family of structurally related pseudotripeptide compounds. Unlike previous methods, our assays did not employ antibodies or reverse-phase extraction steps, only well-to-well transfers, and were easily adapted to a high-throughput automated environment.}, author = {Schmidt, James J. and Stafford, Robert G. and Millard, Charles B.}, citeulike-article-id = {2760314}, citeulike-linkout-0 = {http://dx.doi.org/10.1006/abio.2001.5236}, citeulike-linkout-1 = {http://www.sciencedirect.com/science/article/B6W9V-45BC6P1-50/1/c86a2a4d9b636aa92b4ccd56151de2c7}, day = {1}, doi = {10.1006/abio.2001.5236}, journal = {Analytical Biochemistry}, keywords = {botulinum}, month = {September}, number = {1}, pages = {130--137}, posted-at = {2008-05-06 10:17:33}, priority = {2}, title = {High-Throughput Assays for Botulinum Neurotoxin Proteolytic Activity: Serotypes A, B, D, and F}, url = {http://dx.doi.org/10.1006/abio.2001.5236}, volume = {296}, year = {2001} }

TY - JOUR ID - citeulike:2760314 L3 - citeulike-article-id:2760314 N2 - Botulinum neurotoxins (BoNT) are zinc metalloproteases that cleave and inactivate cellular proteins essential for neurotransmitter release. Because the paralytic effect of BoNT is a consequence of its enzymatic activity, selective inhibitors may be useful as drugs or as tools for further research. To expedite inhibitor discovery, we developed high-throughput, solid-phase protease activity assays for four of the seven BoNT serotypes: A, B, D, and F. Each assay consisted of a cleavable oligopeptide, based on the natural substrate sequence, labeled with fluorescein and covalently attached to maleimide-activated multiwell plates. Solutions of holotoxin or nontoxic catalytic domain of BoNT were incubated in substrate-coated wells, with or without test compounds, followed by transfer and assay of solubilized product in a multiwell fluorometer. Routine toxin concentrations ranged from 10 to 100 ng/ml, but concentrations as low as 2 ng/ml gave reproducible signals. The fluorescence assays were selective, gave very low background readings, and were stable upon prolonged storage. Using the nontoxic catalytic domain of BoNT A, we determined the relative inhibitory potencies of a family of structurally related pseudotripeptide compounds. Unlike previous methods, our assays did not employ antibodies or reverse-phase extraction steps, only well-to-well transfers, and were easily adapted to a high-throughput automated environment. IS - 1 JF - Analytical Biochemistry EP - 137 TI - High-Throughput Assays for Botulinum Neurotoxin Proteolytic Activity: Serotypes A, B, D, and F VL - 296 SP - 130 KW - botulinum AU - Schmidt, James AU - Stafford, Robert AU - Millard, Charles PY - 2001/09/01/ UR - http://dx.doi.org/10.1006/abio.2001.5236 ER -