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Nanopore Sensing of Botulinum Toxin Type B by Discriminating an Enzymatically Cleaved Peptide from a Synaptic Protein Synaptobrevin 2 Derivative
[Image: see text] Botulinum neurotoxins (BoNTs) are the most lethal toxin known to human. Biodefense requires early and rapid detection of BoNTs. Traditionally, BoNTs can be detected by looking for signs of botulism in mice that receive an injection of human material, serum or stool. While the livin...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4296922/ https://www.ncbi.nlm.nih.gov/pubmed/25511125 http://dx.doi.org/10.1021/am5056596 |
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author | Wang, Yong Montana, Vedrana Grubišić, Vladimir Stout, Randy F. Parpura, Vladimir Gu, Li-Qun |
author_facet | Wang, Yong Montana, Vedrana Grubišić, Vladimir Stout, Randy F. Parpura, Vladimir Gu, Li-Qun |
author_sort | Wang, Yong |
collection | PubMed |
description | [Image: see text] Botulinum neurotoxins (BoNTs) are the most lethal toxin known to human. Biodefense requires early and rapid detection of BoNTs. Traditionally, BoNTs can be detected by looking for signs of botulism in mice that receive an injection of human material, serum or stool. While the living animal assay remains the most sensitive approach, it is costly, slow and associated with legal and ethical constrains. Various biochemical, optical and mechanical methods have been developed for BoNTs detection with improved speed, but with lesser sensitivity. Here, we report a novel nanopore-based BoNT type B (BoNT-B) sensor that monitors the toxin’s enzymatic activity on its substrate, a recombinant synaptic protein synaptobrevin 2 derivative. By analyzing the modulation of the pore current caused by the specific BoNT-B-digested peptide as a marker, the presence of BoNT-B at a subnanomolar concentration was identified within minutes. The nanopore detector would fill the niche for a much needed rapid and highly sensitive detection of neurotoxins, and provide an excellent system to explore biophysical mechanisms for biopolymer transportation. |
format | Online Article Text |
id | pubmed-4296922 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-42969222015-12-16 Nanopore Sensing of Botulinum Toxin Type B by Discriminating an Enzymatically Cleaved Peptide from a Synaptic Protein Synaptobrevin 2 Derivative Wang, Yong Montana, Vedrana Grubišić, Vladimir Stout, Randy F. Parpura, Vladimir Gu, Li-Qun ACS Appl Mater Interfaces [Image: see text] Botulinum neurotoxins (BoNTs) are the most lethal toxin known to human. Biodefense requires early and rapid detection of BoNTs. Traditionally, BoNTs can be detected by looking for signs of botulism in mice that receive an injection of human material, serum or stool. While the living animal assay remains the most sensitive approach, it is costly, slow and associated with legal and ethical constrains. Various biochemical, optical and mechanical methods have been developed for BoNTs detection with improved speed, but with lesser sensitivity. Here, we report a novel nanopore-based BoNT type B (BoNT-B) sensor that monitors the toxin’s enzymatic activity on its substrate, a recombinant synaptic protein synaptobrevin 2 derivative. By analyzing the modulation of the pore current caused by the specific BoNT-B-digested peptide as a marker, the presence of BoNT-B at a subnanomolar concentration was identified within minutes. The nanopore detector would fill the niche for a much needed rapid and highly sensitive detection of neurotoxins, and provide an excellent system to explore biophysical mechanisms for biopolymer transportation. American Chemical Society 2014-12-16 2015-01-14 /pmc/articles/PMC4296922/ /pubmed/25511125 http://dx.doi.org/10.1021/am5056596 Text en Copyright © 2014 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Wang, Yong Montana, Vedrana Grubišić, Vladimir Stout, Randy F. Parpura, Vladimir Gu, Li-Qun Nanopore Sensing of Botulinum Toxin Type B by Discriminating an Enzymatically Cleaved Peptide from a Synaptic Protein Synaptobrevin 2 Derivative |
title | Nanopore
Sensing of Botulinum Toxin Type B by Discriminating an Enzymatically
Cleaved Peptide from a Synaptic Protein Synaptobrevin 2 Derivative |
title_full | Nanopore
Sensing of Botulinum Toxin Type B by Discriminating an Enzymatically
Cleaved Peptide from a Synaptic Protein Synaptobrevin 2 Derivative |
title_fullStr | Nanopore
Sensing of Botulinum Toxin Type B by Discriminating an Enzymatically
Cleaved Peptide from a Synaptic Protein Synaptobrevin 2 Derivative |
title_full_unstemmed | Nanopore
Sensing of Botulinum Toxin Type B by Discriminating an Enzymatically
Cleaved Peptide from a Synaptic Protein Synaptobrevin 2 Derivative |
title_short | Nanopore
Sensing of Botulinum Toxin Type B by Discriminating an Enzymatically
Cleaved Peptide from a Synaptic Protein Synaptobrevin 2 Derivative |
title_sort | nanopore
sensing of botulinum toxin type b by discriminating an enzymatically
cleaved peptide from a synaptic protein synaptobrevin 2 derivative |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4296922/ https://www.ncbi.nlm.nih.gov/pubmed/25511125 http://dx.doi.org/10.1021/am5056596 |
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