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Characterization and evaluation of the enzymatic activity of tetanus toxin submitted to cobalt-60 gamma radiation
BACKGROUND: Tetanus toxin blocks the release of the inhibitory neurotransmitters in the central nervous system and causes tetanus and its main form of prevention is through vaccination. The vaccine is produced by inactivation of tetanus toxin with formaldehyde, which may cause side effects. An alter...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Centro de Estudos de Venenos e Animais Peçonhentos
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8092855/ https://www.ncbi.nlm.nih.gov/pubmed/33995513 http://dx.doi.org/10.1590/1678-9199-JVATITD-2020-0140 |
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author | Sartori, Giselle Pacifico da Costa, Andréa Macarini, Fernanda Lúcio dos Santos Mariano, Douglas Oscar Ceolin Pimenta, Daniel Carvalho Spencer, Patrick Jack Nali, Luiz Henrique da Silva Galisteo, Andrés Jimenez |
author_facet | Sartori, Giselle Pacifico da Costa, Andréa Macarini, Fernanda Lúcio dos Santos Mariano, Douglas Oscar Ceolin Pimenta, Daniel Carvalho Spencer, Patrick Jack Nali, Luiz Henrique da Silva Galisteo, Andrés Jimenez |
author_sort | Sartori, Giselle Pacifico |
collection | PubMed |
description | BACKGROUND: Tetanus toxin blocks the release of the inhibitory neurotransmitters in the central nervous system and causes tetanus and its main form of prevention is through vaccination. The vaccine is produced by inactivation of tetanus toxin with formaldehyde, which may cause side effects. An alternative way is the use of ionizing radiation for inactivation of the toxin and also to improve the potential immunogenic response and to reduce the post-vaccination side effects. Therefore, the aim of this study was to characterize the tetanus toxin structure after different doses of ionizing radiation of (60)Co. METHODS: Irradiated and native tetanus toxin was characterized by SDS PAGE in reducing and non-reducing conditions and MALD-TOF. Enzymatic activity was measured by FRET substrate. Also, antigenic properties were assessed by ELISA and Western Blot data. RESULTS: Characterization analysis revealed gradual modification on the tetanus toxin structure according to doses increase. Also, fragmentation and possible aggregations of the protein fragments were observed in higher doses. In the analysis of peptide preservation by enzymatic digestion and mass spectrometry, there was a slight modification in the identification up to the dose of 4 kGy. At subsequent doses, peptide identification was minimal. The analysis of the enzymatic activity by fluorescence showed 35 % attenuation in the activity even at higher doses. In the antigenic evaluation, anti-tetanus toxin antibodies were detected against the irradiated toxins at the different doses, with a gradual decrease as the dose increased, but remaining at satisfactory levels. CONCLUSION: Ionizing radiation promoted structural changes in the tetanus toxin such as fragmentation and/or aggregation and attenuation of enzymatic activity as the dose increased, but antigenic recognition of the toxin remained at good levels indicating its possible use as an immunogen. However, studies of enzymatic activity of tetanus toxin irradiated with doses above 8 kGy should be further analyzed. |
format | Online Article Text |
id | pubmed-8092855 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Centro de Estudos de Venenos e Animais Peçonhentos |
record_format | MEDLINE/PubMed |
spelling | pubmed-80928552021-05-13 Characterization and evaluation of the enzymatic activity of tetanus toxin submitted to cobalt-60 gamma radiation Sartori, Giselle Pacifico da Costa, Andréa Macarini, Fernanda Lúcio dos Santos Mariano, Douglas Oscar Ceolin Pimenta, Daniel Carvalho Spencer, Patrick Jack Nali, Luiz Henrique da Silva Galisteo, Andrés Jimenez J Venom Anim Toxins Incl Trop Dis Research BACKGROUND: Tetanus toxin blocks the release of the inhibitory neurotransmitters in the central nervous system and causes tetanus and its main form of prevention is through vaccination. The vaccine is produced by inactivation of tetanus toxin with formaldehyde, which may cause side effects. An alternative way is the use of ionizing radiation for inactivation of the toxin and also to improve the potential immunogenic response and to reduce the post-vaccination side effects. Therefore, the aim of this study was to characterize the tetanus toxin structure after different doses of ionizing radiation of (60)Co. METHODS: Irradiated and native tetanus toxin was characterized by SDS PAGE in reducing and non-reducing conditions and MALD-TOF. Enzymatic activity was measured by FRET substrate. Also, antigenic properties were assessed by ELISA and Western Blot data. RESULTS: Characterization analysis revealed gradual modification on the tetanus toxin structure according to doses increase. Also, fragmentation and possible aggregations of the protein fragments were observed in higher doses. In the analysis of peptide preservation by enzymatic digestion and mass spectrometry, there was a slight modification in the identification up to the dose of 4 kGy. At subsequent doses, peptide identification was minimal. The analysis of the enzymatic activity by fluorescence showed 35 % attenuation in the activity even at higher doses. In the antigenic evaluation, anti-tetanus toxin antibodies were detected against the irradiated toxins at the different doses, with a gradual decrease as the dose increased, but remaining at satisfactory levels. CONCLUSION: Ionizing radiation promoted structural changes in the tetanus toxin such as fragmentation and/or aggregation and attenuation of enzymatic activity as the dose increased, but antigenic recognition of the toxin remained at good levels indicating its possible use as an immunogen. However, studies of enzymatic activity of tetanus toxin irradiated with doses above 8 kGy should be further analyzed. Centro de Estudos de Venenos e Animais Peçonhentos 2021-04-30 /pmc/articles/PMC8092855/ /pubmed/33995513 http://dx.doi.org/10.1590/1678-9199-JVATITD-2020-0140 Text en https://creativecommons.org/licenses/by/4.0/© The Author(s). 2021 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (https://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Sartori, Giselle Pacifico da Costa, Andréa Macarini, Fernanda Lúcio dos Santos Mariano, Douglas Oscar Ceolin Pimenta, Daniel Carvalho Spencer, Patrick Jack Nali, Luiz Henrique da Silva Galisteo, Andrés Jimenez Characterization and evaluation of the enzymatic activity of tetanus toxin submitted to cobalt-60 gamma radiation |
title | Characterization and evaluation of the enzymatic activity of tetanus
toxin submitted to cobalt-60 gamma radiation |
title_full | Characterization and evaluation of the enzymatic activity of tetanus
toxin submitted to cobalt-60 gamma radiation |
title_fullStr | Characterization and evaluation of the enzymatic activity of tetanus
toxin submitted to cobalt-60 gamma radiation |
title_full_unstemmed | Characterization and evaluation of the enzymatic activity of tetanus
toxin submitted to cobalt-60 gamma radiation |
title_short | Characterization and evaluation of the enzymatic activity of tetanus
toxin submitted to cobalt-60 gamma radiation |
title_sort | characterization and evaluation of the enzymatic activity of tetanus
toxin submitted to cobalt-60 gamma radiation |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8092855/ https://www.ncbi.nlm.nih.gov/pubmed/33995513 http://dx.doi.org/10.1590/1678-9199-JVATITD-2020-0140 |
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