Produção de anticorpos contra metaloproteases e crotoxina usando antígenos sintéticos e caracterização proteômica e toxicológica do veneno de Bothrops brazili
| Ano de defesa: | 2020 |
|---|---|
| Autor(a) principal: | |
| Orientador(a): | |
| Banca de defesa: | |
| Tipo de documento: | Tese |
| Tipo de acesso: | Acesso aberto |
| Idioma: | por |
| Instituição de defesa: |
Universidade Federal de Minas Gerais
|
| Programa de Pós-Graduação: |
Não Informado pela instituição
|
| Departamento: |
Não Informado pela instituição
|
| País: |
Não Informado pela instituição
|
| Palavras-chave em Português: | |
| Link de acesso: | https://hdl.handle.net/1843/34836 |
Resumo: | Snakes belonging to the genera Bothrops, Crotalus, Lachesis and Micrurus are responsible for most cases of snakebites in Brazil. Snakes of the genus Crotalus spp and Micrurus spp have neurotoxic venom with high lethality if not neutralized in time. Bothrops and Lachesis venom display proteolytic action, causing permanent damage even after treatment with antiofidic sera. The traditional use of venoms in the immunization of animals for the production of antiofidic sera have drawbacks, since the immunized animals may suffer because of toxic components of the venom, which reduces their life expectancy. Beside, the extensive inter and intraspecific variability in the biochemical composition of snake venoms can affect the neutralizing efficacy of antiofidic sera. Thus, it is crucial to use new technologies to search for and produce alternative non-toxic immunogens that can be used in the production of antiofidic serums. The use of synthetic peptides and multiepitopic proteins that mimic epitopes of the main toxins of each venom would be an alternative for the production of neutralizing antibodies with less impact on experimental animals. This work is presented in the format of three articles, each one containing in a separated chapter of results. Each chapter presents its individualized abstract. The content description of each chapter is shown below: Chapter 1, (Article 1 - Identification of a linear B-cell epitope in the catalytic domain of bothropasin, metalloproteinase from Bothrops jararaca snake venom), this article describes the mapping and synthesis of a linear B cell epitope for bothropasin, capable of to induce neutralizing antibodies. Chapter 2, (Article 2 - Engineered protein containing Crotoxin epitopes induces neutralizing antibodies in immunized rabbits), this article descridbes the production of a multiepitopic recombinant crotoxin protein, capable of inducing neutralizing antibodies. Chapter 3, (Article 3 - Proteomic and toxinological characterization of Peruvian pitviper Bothrops brazili ("jergón shushupe"), venom.), In this article, the components of Bothrops brazili (BbV) venom were analyzed by RP-HPLC, SDS-PAGE and MALDI-TOF/TOF, showing that snake venom metalloproteinases (SVMPs) were the most abundant proteins in the venom of B. brazili. Each article presents its discussion separately. At the end of the third article a general discussion of the three articles is presented. |
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Produção de anticorpos contra metaloproteases e crotoxina usando antígenos sintéticos e caracterização proteômica e toxicológica do veneno de Bothrops braziliProduction of antibodies against metalloproteases and crotoxin using synthetic antigens and proteomic and toxicological characterization of Bothrops brazili venomSerpentesHemorragiaCrotoxinaMetaloproteasesFormação de anticorposCrotoxinaBothropasinaEpitópoVeneno de serpentesBothrops braziiAnalise proteomicosínteses de peptídeosmetaloproteasesSnakes belonging to the genera Bothrops, Crotalus, Lachesis and Micrurus are responsible for most cases of snakebites in Brazil. Snakes of the genus Crotalus spp and Micrurus spp have neurotoxic venom with high lethality if not neutralized in time. Bothrops and Lachesis venom display proteolytic action, causing permanent damage even after treatment with antiofidic sera. The traditional use of venoms in the immunization of animals for the production of antiofidic sera have drawbacks, since the immunized animals may suffer because of toxic components of the venom, which reduces their life expectancy. Beside, the extensive inter and intraspecific variability in the biochemical composition of snake venoms can affect the neutralizing efficacy of antiofidic sera. Thus, it is crucial to use new technologies to search for and produce alternative non-toxic immunogens that can be used in the production of antiofidic serums. The use of synthetic peptides and multiepitopic proteins that mimic epitopes of the main toxins of each venom would be an alternative for the production of neutralizing antibodies with less impact on experimental animals. This work is presented in the format of three articles, each one containing in a separated chapter of results. Each chapter presents its individualized abstract. The content description of each chapter is shown below: Chapter 1, (Article 1 - Identification of a linear B-cell epitope in the catalytic domain of bothropasin, metalloproteinase from Bothrops jararaca snake venom), this article describes the mapping and synthesis of a linear B cell epitope for bothropasin, capable of to induce neutralizing antibodies. Chapter 2, (Article 2 - Engineered protein containing Crotoxin epitopes induces neutralizing antibodies in immunized rabbits), this article descridbes the production of a multiepitopic recombinant crotoxin protein, capable of inducing neutralizing antibodies. Chapter 3, (Article 3 - Proteomic and toxinological characterization of Peruvian pitviper Bothrops brazili ("jergón shushupe"), venom.), In this article, the components of Bothrops brazili (BbV) venom were analyzed by RP-HPLC, SDS-PAGE and MALDI-TOF/TOF, showing that snake venom metalloproteinases (SVMPs) were the most abundant proteins in the venom of B. brazili. Each article presents its discussion separately. At the end of the third article a general discussion of the three articles is presented.CAPES - Coordenação de Aperfeiçoamento de Pessoal de Nível SuperiorUniversidade Federal de Minas Gerais2021-01-21T21:00:19Z2025-09-09T01:01:33Z2021-01-21T21:00:19Z2020-09-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisapplication/pdfhttps://hdl.handle.net/1843/34836porhttp://creativecommons.org/licenses/by-nc-nd/3.0/pt/info:eu-repo/semantics/openAccessDenis Alexis Molina Molinareponame:Repositório Institucional da UFMGinstname:Universidade Federal de Minas Gerais (UFMG)instacron:UFMG2025-09-09T01:01:33Zoai:repositorio.ufmg.br:1843/34836Repositório InstitucionalPUBhttps://repositorio.ufmg.br/oairepositorio@ufmg.bropendoar:2025-09-09T01:01:33Repositório Institucional da UFMG - Universidade Federal de Minas Gerais (UFMG)false |
| dc.title.none.fl_str_mv |
Produção de anticorpos contra metaloproteases e crotoxina usando antígenos sintéticos e caracterização proteômica e toxicológica do veneno de Bothrops brazili Production of antibodies against metalloproteases and crotoxin using synthetic antigens and proteomic and toxicological characterization of Bothrops brazili venom |
| title |
Produção de anticorpos contra metaloproteases e crotoxina usando antígenos sintéticos e caracterização proteômica e toxicológica do veneno de Bothrops brazili |
| spellingShingle |
Produção de anticorpos contra metaloproteases e crotoxina usando antígenos sintéticos e caracterização proteômica e toxicológica do veneno de Bothrops brazili Denis Alexis Molina Molina Serpentes Hemorragia Crotoxina Metaloproteases Formação de anticorpos Crotoxina Bothropasina Epitópo Veneno de serpentes Bothrops brazii Analise proteomico sínteses de peptídeos metaloproteases |
| title_short |
Produção de anticorpos contra metaloproteases e crotoxina usando antígenos sintéticos e caracterização proteômica e toxicológica do veneno de Bothrops brazili |
| title_full |
Produção de anticorpos contra metaloproteases e crotoxina usando antígenos sintéticos e caracterização proteômica e toxicológica do veneno de Bothrops brazili |
| title_fullStr |
Produção de anticorpos contra metaloproteases e crotoxina usando antígenos sintéticos e caracterização proteômica e toxicológica do veneno de Bothrops brazili |
| title_full_unstemmed |
Produção de anticorpos contra metaloproteases e crotoxina usando antígenos sintéticos e caracterização proteômica e toxicológica do veneno de Bothrops brazili |
| title_sort |
Produção de anticorpos contra metaloproteases e crotoxina usando antígenos sintéticos e caracterização proteômica e toxicológica do veneno de Bothrops brazili |
| author |
Denis Alexis Molina Molina |
| author_facet |
Denis Alexis Molina Molina |
| author_role |
author |
| dc.contributor.author.fl_str_mv |
Denis Alexis Molina Molina |
| dc.subject.por.fl_str_mv |
Serpentes Hemorragia Crotoxina Metaloproteases Formação de anticorpos Crotoxina Bothropasina Epitópo Veneno de serpentes Bothrops brazii Analise proteomico sínteses de peptídeos metaloproteases |
| topic |
Serpentes Hemorragia Crotoxina Metaloproteases Formação de anticorpos Crotoxina Bothropasina Epitópo Veneno de serpentes Bothrops brazii Analise proteomico sínteses de peptídeos metaloproteases |
| description |
Snakes belonging to the genera Bothrops, Crotalus, Lachesis and Micrurus are responsible for most cases of snakebites in Brazil. Snakes of the genus Crotalus spp and Micrurus spp have neurotoxic venom with high lethality if not neutralized in time. Bothrops and Lachesis venom display proteolytic action, causing permanent damage even after treatment with antiofidic sera. The traditional use of venoms in the immunization of animals for the production of antiofidic sera have drawbacks, since the immunized animals may suffer because of toxic components of the venom, which reduces their life expectancy. Beside, the extensive inter and intraspecific variability in the biochemical composition of snake venoms can affect the neutralizing efficacy of antiofidic sera. Thus, it is crucial to use new technologies to search for and produce alternative non-toxic immunogens that can be used in the production of antiofidic serums. The use of synthetic peptides and multiepitopic proteins that mimic epitopes of the main toxins of each venom would be an alternative for the production of neutralizing antibodies with less impact on experimental animals. This work is presented in the format of three articles, each one containing in a separated chapter of results. Each chapter presents its individualized abstract. The content description of each chapter is shown below: Chapter 1, (Article 1 - Identification of a linear B-cell epitope in the catalytic domain of bothropasin, metalloproteinase from Bothrops jararaca snake venom), this article describes the mapping and synthesis of a linear B cell epitope for bothropasin, capable of to induce neutralizing antibodies. Chapter 2, (Article 2 - Engineered protein containing Crotoxin epitopes induces neutralizing antibodies in immunized rabbits), this article descridbes the production of a multiepitopic recombinant crotoxin protein, capable of inducing neutralizing antibodies. Chapter 3, (Article 3 - Proteomic and toxinological characterization of Peruvian pitviper Bothrops brazili ("jergón shushupe"), venom.), In this article, the components of Bothrops brazili (BbV) venom were analyzed by RP-HPLC, SDS-PAGE and MALDI-TOF/TOF, showing that snake venom metalloproteinases (SVMPs) were the most abundant proteins in the venom of B. brazili. Each article presents its discussion separately. At the end of the third article a general discussion of the three articles is presented. |
| publishDate |
2020 |
| dc.date.none.fl_str_mv |
2020-09-01 2021-01-21T21:00:19Z 2021-01-21T21:00:19Z 2025-09-09T01:01:33Z |
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info:eu-repo/semantics/publishedVersion |
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info:eu-repo/semantics/doctoralThesis |
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doctoralThesis |
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publishedVersion |
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https://hdl.handle.net/1843/34836 |
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https://hdl.handle.net/1843/34836 |
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por |
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por |
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http://creativecommons.org/licenses/by-nc-nd/3.0/pt/ info:eu-repo/semantics/openAccess |
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http://creativecommons.org/licenses/by-nc-nd/3.0/pt/ |
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Universidade Federal de Minas Gerais |
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Universidade Federal de Minas Gerais |
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reponame:Repositório Institucional da UFMG instname:Universidade Federal de Minas Gerais (UFMG) instacron:UFMG |
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Universidade Federal de Minas Gerais (UFMG) |
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