Clonagem e expressão da toxina TX3-1 do veneno da aranha phneutria nigriventer
| Ano de defesa: | 2008 |
|---|---|
| Autor(a) principal: | |
| Orientador(a): | |
| Banca de defesa: | |
| Tipo de documento: | Dissertação |
| 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/CMFC-7FJQUJ |
Resumo: | The toxin Tx3-1 purified from the spider venom Phoneutria nigriventer is a blocker of potassium channels with great pharmacological potential. However the purification of the toxin from Phoneutria nigriventer crude venom is a long and expensive process. The objective of this work was standardize techniques of molecular biology that would allow the expression and purification in large scale of functional recombinant Tx3-1.We cloned and expressed the toxin Tx3-1 tagged to the C-terminus of the maltose binding protein (MBP) in the cytoplasm of E. coli BL21. The hybrid protein purification was performed by affinity chromatography (amylase column). After purification, MBP-TX3-1 was cleaved by Factor Xa and recombinant Tx3-1 was purified by gel filtration using Superdex 75 column in FPLC system. Both, fusion protein MBP/Tx3-1 and recombinant Tx3-1 reacted with anti-Phoneutria nigriventer venom antibodies.The biological activity of recombinant toxin Tx3-1 was tested in biological assays and compared to native toxin biological activity. In experiments using rats cardiomyocytes, recombinant Tx3-1 toxin was able to increase the calcium transient in 20%, similarly to native toxin. Treatment of isolated rat hearts and atriums with recombinant Tx3-1, and native toxin, led to decrease in arrhythmia. These data suggest that the recombinant and native Tx3-1 probably present the same three-dimensional structure and function. These results open up the possibility of using the recombinant Tx3-1 to determine the molecular structure and action mechanisms of Tx3-1. Moreover, the recombinant protein enables the possibility of using the toxin Tx3-1 as a therapeutic drug for prevention and treatment of hearts diseases. |
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2019-08-11T04:09:59Z2025-09-09T01:15:38Z2019-08-11T04:09:59Z2008-05-28https://hdl.handle.net/1843/CMFC-7FJQUJThe toxin Tx3-1 purified from the spider venom Phoneutria nigriventer is a blocker of potassium channels with great pharmacological potential. However the purification of the toxin from Phoneutria nigriventer crude venom is a long and expensive process. The objective of this work was standardize techniques of molecular biology that would allow the expression and purification in large scale of functional recombinant Tx3-1.We cloned and expressed the toxin Tx3-1 tagged to the C-terminus of the maltose binding protein (MBP) in the cytoplasm of E. coli BL21. The hybrid protein purification was performed by affinity chromatography (amylase column). After purification, MBP-TX3-1 was cleaved by Factor Xa and recombinant Tx3-1 was purified by gel filtration using Superdex 75 column in FPLC system. Both, fusion protein MBP/Tx3-1 and recombinant Tx3-1 reacted with anti-Phoneutria nigriventer venom antibodies.The biological activity of recombinant toxin Tx3-1 was tested in biological assays and compared to native toxin biological activity. In experiments using rats cardiomyocytes, recombinant Tx3-1 toxin was able to increase the calcium transient in 20%, similarly to native toxin. Treatment of isolated rat hearts and atriums with recombinant Tx3-1, and native toxin, led to decrease in arrhythmia. These data suggest that the recombinant and native Tx3-1 probably present the same three-dimensional structure and function. These results open up the possibility of using the recombinant Tx3-1 to determine the molecular structure and action mechanisms of Tx3-1. Moreover, the recombinant protein enables the possibility of using the toxin Tx3-1 as a therapeutic drug for prevention and treatment of hearts diseases.Universidade Federal de Minas GeraisPHONEUTRIA NIGRIVENTERAranha VenenoBioquímicaClonagem e expressão da toxina TX3-1 do veneno da aranha phneutria nigriventerinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisAndrea Cristina Gomes Piresinfo:eu-repo/semantics/openAccessporreponame:Repositório Institucional da UFMGinstname:Universidade Federal de Minas Gerais (UFMG)instacron:UFMGVania Ferreira PradoMarcus Vinicios GomezCarlos Delfin Chavez OlorteguiA toxina Tx3-1 purificada do veneno da aranha Phoneutria nigriventer, é um bloqueador de canais de potássio, com grande potencial farmacológico. Porém a purificação dessa toxina a partir do veneno total da aranha Phoneutria nigriventer é um processo longo e dispendioso. O objetivo desse trabalho foi padronizar técnicas de biologia molecular que permitissem a expressão e purificação de grandes quantidades da toxina Tx3-1 recombinante com características funcionais semelhantes à da proteína nativa. Nós clonamos e expressamos a toxina Tx3-1 como um híbrido ligado a proteína ligadora de maltose (MBP) no citoplasma de E.coli BL21. Após purificação desta proteína híbrida por cromatografia de afinidade (coluna de amilose), a MBP-TX3-1 foi clivada por Fator Xa e a Tx3-1 recombinante foi purificada por gel filtração em coluna Superdex 75 em Sistema FPLC. Tanto a proteína de fusão MBP/Tx3-1 quanto a Tx3-1 recombinante reagiu com anticorpos antiveneno total da aranha Phoneutria nigriventer, indicando que a toxina foi clonada em fase de leitura correta. A atividade biológica da toxina Tx3-1 recombinante foi testada em ensaios biológicos e comparada com a atividade da toxina nativa. Semelhantemente à toxina nativa, em ensaios utilizando cardiomócitos de rato a toxina Tx3-1 recombinante foi capaz de aumentar a amplitude do cálcio transiente em 20%, quando comparada ao controle. Em ensaios com coração e átrios isolados de rato, a Tx3-1 recombinante apresentou efeito semelhante ao da Toxina Tx3-1 nativa, na redução do tempo de arritmia. Esses dados sugerem que a toxina Tx3-1 recombinante e a nativa apresentam a mesma estrutura tridimensional e abrem a possibilidade de utilizarmos a Tx3-1 recombinante para determinação da estrutura molecular da toxina e também para obter detalhes sobre o mecanismo molecular da ação da toxina. Além disso, a Tx3-1 recombinante viabiliza a possibilidade de utilização da toxina Tx3-1 como agente terapêutico para prevenção e tratamento de distúrbios cardíacos.UFMGORIGINALandr_a_cristina_g_mez_pires_resumo.pdfapplication/pdf23960https://repositorio.ufmg.br//bitstreams/8c3cce79-0ccb-494d-a58b-36355f24d9ff/downloadf66580263595a782d226b26584eea763MD51trueAnonymousREADTEXTandr_a_cristina_g_mez_pires_resumo.pdf.txttext/plain4012https://repositorio.ufmg.br//bitstreams/6bbfdee4-59a3-4ff1-8b8e-3f274c05fd9f/download945e0c023b22aa3fa600e69e8aaf16faMD52falseAnonymousREADTHUMBNAILandr_a_cristina_g_mez_pires_resumo.pdf.jpgandr_a_cristina_g_mez_pires_resumo.pdf.jpgGenerated Thumbnailimage/jpeg5174https://repositorio.ufmg.br//bitstreams/dd4a82d3-fad9-4781-b2fb-aaa6286820e8/download7b87de031b9b58e4619c791ba3773e47MD53falseAnonymousREAD1843/CMFC-7FJQUJ2025-09-09 15:45:28.253open.accessoai:repositorio.ufmg.br:1843/CMFC-7FJQUJhttps://repositorio.ufmg.br/Repositório InstitucionalPUBhttps://repositorio.ufmg.br/oairepositorio@ufmg.bropendoar:2025-09-09T18:45:28Repositório Institucional da UFMG - Universidade Federal de Minas Gerais (UFMG)false |
| dc.title.none.fl_str_mv |
Clonagem e expressão da toxina TX3-1 do veneno da aranha phneutria nigriventer |
| title |
Clonagem e expressão da toxina TX3-1 do veneno da aranha phneutria nigriventer |
| spellingShingle |
Clonagem e expressão da toxina TX3-1 do veneno da aranha phneutria nigriventer Andrea Cristina Gomes Pires Aranha Veneno Bioquímica PHONEUTRIA NIGRIVENTER |
| title_short |
Clonagem e expressão da toxina TX3-1 do veneno da aranha phneutria nigriventer |
| title_full |
Clonagem e expressão da toxina TX3-1 do veneno da aranha phneutria nigriventer |
| title_fullStr |
Clonagem e expressão da toxina TX3-1 do veneno da aranha phneutria nigriventer |
| title_full_unstemmed |
Clonagem e expressão da toxina TX3-1 do veneno da aranha phneutria nigriventer |
| title_sort |
Clonagem e expressão da toxina TX3-1 do veneno da aranha phneutria nigriventer |
| author |
Andrea Cristina Gomes Pires |
| author_facet |
Andrea Cristina Gomes Pires |
| author_role |
author |
| dc.contributor.author.fl_str_mv |
Andrea Cristina Gomes Pires |
| dc.subject.por.fl_str_mv |
Aranha Veneno Bioquímica |
| topic |
Aranha Veneno Bioquímica PHONEUTRIA NIGRIVENTER |
| dc.subject.other.none.fl_str_mv |
PHONEUTRIA NIGRIVENTER |
| description |
The toxin Tx3-1 purified from the spider venom Phoneutria nigriventer is a blocker of potassium channels with great pharmacological potential. However the purification of the toxin from Phoneutria nigriventer crude venom is a long and expensive process. The objective of this work was standardize techniques of molecular biology that would allow the expression and purification in large scale of functional recombinant Tx3-1.We cloned and expressed the toxin Tx3-1 tagged to the C-terminus of the maltose binding protein (MBP) in the cytoplasm of E. coli BL21. The hybrid protein purification was performed by affinity chromatography (amylase column). After purification, MBP-TX3-1 was cleaved by Factor Xa and recombinant Tx3-1 was purified by gel filtration using Superdex 75 column in FPLC system. Both, fusion protein MBP/Tx3-1 and recombinant Tx3-1 reacted with anti-Phoneutria nigriventer venom antibodies.The biological activity of recombinant toxin Tx3-1 was tested in biological assays and compared to native toxin biological activity. In experiments using rats cardiomyocytes, recombinant Tx3-1 toxin was able to increase the calcium transient in 20%, similarly to native toxin. Treatment of isolated rat hearts and atriums with recombinant Tx3-1, and native toxin, led to decrease in arrhythmia. These data suggest that the recombinant and native Tx3-1 probably present the same three-dimensional structure and function. These results open up the possibility of using the recombinant Tx3-1 to determine the molecular structure and action mechanisms of Tx3-1. Moreover, the recombinant protein enables the possibility of using the toxin Tx3-1 as a therapeutic drug for prevention and treatment of hearts diseases. |
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2008 |
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2008-05-28 |
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2019-08-11T04:09:59Z 2025-09-09T01:15:38Z |
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2019-08-11T04:09:59Z |
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info:eu-repo/semantics/publishedVersion |
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info:eu-repo/semantics/masterThesis |
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https://hdl.handle.net/1843/CMFC-7FJQUJ |
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por |
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Universidade Federal de Minas Gerais |
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Universidade Federal de Minas Gerais |
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