Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/65194
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dc.contributor.authorVV, Vaidyanathan-
dc.contributor.authorK, Saravanan-
dc.contributor.authorR, Sistla-
dc.contributor.authorT, Binz-
dc.date.accessioned2025-01-07T04:56:57Z-
dc.date.available2025-01-07T04:56:57Z-
dc.date.issued2025-01-
dc.identifier.issn0975-0959 (Online), 0301-1208 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/65194-
dc.description161-168en_US
dc.description.abstractThere are concerns on use of Botulinum neurotoxin type A (BoNT/A) as a bioweapon and effective small molecule antidotes to treat toxin poisoning are required. Five phytochemicals with known medicinal properties were evaluated for their ability to bind at the active site of Botulinum neurotoxin A light chain (LC/A). In silico docking studies showed that natural flavonoid Quercetagetin interacts with critical amino acid residues in the catalytic pocket and substrate discriminating sub-site regions of the light chain. Using an in vitro protease assay with a radiolabeled derivative of the native SNAP-25 substrate and recombinant LC/A, we tested the inhibitory potency of the phytochemicals. Quercetagetin was found to inhibit toxin’s protease activity with an IC50 of ~ 26 µM. Our study shows that Quercetagetin displays potential to block BoNT/A, and its core benzopyranone scaffold holds promise for developing useful inhibitors to treat botulism.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR, Indiaen_US
dc.sourceIJBB Vol.62(02) [February 2025]en_US
dc.subjectBotulinum toxin type Aen_US
dc.subjectIn silico docking analysisen_US
dc.subjectInhibitionen_US
dc.subjectProtease activityen_US
dc.subjectQuercetagetinen_US
dc.titleInhibition of Botulinum neurotoxin A protease activity by Quercetagetinen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.56042/ijbb.v62i2.12118en_US
Appears in Collections:IJBB Vol.62(02) [February 2025]

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