Desenvolvimento e aplicação de biorreatores capilares para a triagem de ligantes de Purina Nucleosídeo Fosforilases

Detalhes bibliográficos
Autor(a) principal: Moraes, Marcela Cristina de
Data de Publicação: 2012
Tipo de documento: Tese
Idioma: por
Título da fonte: Repositório Institucional da UFSCAR
Texto Completo: https://repositorio.ufscar.br/handle/ufscar/6220
Resumo: Purine Nucleoside Phosphorylases (PNPs) are key enzymes of the purine salvage pathway, and therefore are considered attractive targets for new drugs search. In this context, the development of effective and selective bioassays for PNP ligands screening is an important task. This work describes the covalent immobilization of human and Schistossoma mansoni PNP on fused silica capillaries. The activity of the immobilized enzyme reactors (IMERs) was monitored on line, employing multidimensional zonal chromatography, by the quantification of the product formed throughout the enzymatic reaction. This method enabled the determination of kinetic constants, screening, identification and characterization of enzymatic inhibitors. Two potent human PNP inhibitors were recognized and characterized. Through the use of inhibitors with different potencies, previously characterized by zonal chromatography, the affinity-based ligands screening employing frontal chromatography was validated. Frontal affinity chromatography analysis demonstrated to be a valuable method for the rapid identification of new ligands, while the main advantage of the multidimensional zonal chromatography method herein described consists on the ability to directly evaluate the effect of the ligands in the biological function of these enzymes. The methods described in this work represent an improvement to the PNPs inhibitors consolidated screening assays, since they directly quantify the enzymatic reaction product or are able to rank the inhibitors according to their affinities, resulting in a rapid automated analysis and false positives free.
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spelling Moraes, Marcela Cristina deCass, Quezia Bezerrahttp://genos.cnpq.br:12010/dwlattes/owa/prc_imp_cv_int?f_cod=K4781559E6http://lattes.cnpq.br/40923287240863085653cb50-4b39-401a-bf1a-3708dbbec8322016-06-02T20:34:33Z2012-03-192016-06-02T20:34:33Z2012-02-28MORAES, Marcela Cristina de. Development and application of capillary bioreactors for screening of Purine Nucleoside Phosphorylases ligands. 2012. 150 f. Tese (Doutorado em Ciências Exatas e da Terra) - Universidade Federal de São Carlos, São Carlos, 2012.https://repositorio.ufscar.br/handle/ufscar/6220Purine Nucleoside Phosphorylases (PNPs) are key enzymes of the purine salvage pathway, and therefore are considered attractive targets for new drugs search. In this context, the development of effective and selective bioassays for PNP ligands screening is an important task. This work describes the covalent immobilization of human and Schistossoma mansoni PNP on fused silica capillaries. The activity of the immobilized enzyme reactors (IMERs) was monitored on line, employing multidimensional zonal chromatography, by the quantification of the product formed throughout the enzymatic reaction. This method enabled the determination of kinetic constants, screening, identification and characterization of enzymatic inhibitors. Two potent human PNP inhibitors were recognized and characterized. Through the use of inhibitors with different potencies, previously characterized by zonal chromatography, the affinity-based ligands screening employing frontal chromatography was validated. Frontal affinity chromatography analysis demonstrated to be a valuable method for the rapid identification of new ligands, while the main advantage of the multidimensional zonal chromatography method herein described consists on the ability to directly evaluate the effect of the ligands in the biological function of these enzymes. The methods described in this work represent an improvement to the PNPs inhibitors consolidated screening assays, since they directly quantify the enzymatic reaction product or are able to rank the inhibitors according to their affinities, resulting in a rapid automated analysis and false positives free.Purina Nucleosídeo Fosforilases (PNPs) são enzimas chave na via de salvação de purinas, e por isso são consideradas alvos atrativos para a busca por novos fármacos. Nesse contexto, o desenvolvimento de bioensaios seletivos e eficazes para a triagem de novos ligantes das PNPs é de importância crucial. Este trabalho descreve a imobilização covalente das PNPs humana e de Schistosoma mansoni em capilares de sílica fundida. A atividade das enzimas imobilizadas (IMERs) foi monitorada on line, por cromatografia zonal multidimensional, através da quantificação do produto formado na reação enzimática. Este método possibilitou a determinação das constantes cinéticas, a triagem, identificação e caracterização de inibidores enzimáticos. Dois inibidores potentes da PNP humana foram reconhecidos e caracterizados. Através do uso destes inibidores de diferentes potências, previamente caracterizados por cromatografia zonal, a triagem de ligantes por afinidade empregando a cromatografia frontal foi validada para o IMER baseado na PNP humana. As análises por cromatografia de afinidade frontal demonstraram ser uma estratégia valiosa na identificação rápida de novos ligantes, enquanto o método multidimensional desenvolvido apresenta como principal vantagem a capacidade de avaliar diretamente o efeito dos ligantes na função biológica destas enzimas. Os métodos descritos neste trabalho representam um avanço aos métodos consolidados de triagem de inibidores das PNPs, pois quantifica diretamente o produto formado da reação enzimática ou os classifica por afinidade, resultando em análises rápidas, automatizadas e sem falsos positivos.Universidade Federal de Minas Geraisapplication/pdfporUniversidade Federal de São CarlosPrograma de Pós-Graduação em Química - PPGQUFSCarBRQuímicaImobilização de enzimasEnsaios enzimáticosCIENCIAS EXATAS E DA TERRA::QUIMICADesenvolvimento e aplicação de biorreatores capilares para a triagem de ligantes de Purina Nucleosídeo FosforilasesDevelopment and application of capillary bioreactors for screening of Purine Nucleoside Phosphorylases ligandsinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesis-1-1867fc213-f339-49e1-a669-a1e54cf68bf1info:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFSCARinstname:Universidade Federal de São Carlos (UFSCAR)instacron:UFSCARORIGINAL4136.pdfapplication/pdf5493903https://repositorio.ufscar.br/bitstream/ufscar/6220/1/4136.pdf43bf6490c910378ad1f093d9b1f60982MD51THUMBNAIL4136.pdf.jpg4136.pdf.jpgIM Thumbnailimage/jpeg10415https://repositorio.ufscar.br/bitstream/ufscar/6220/2/4136.pdf.jpgff97560f61574c2069f2074d16f695deMD52ufscar/62202023-09-18 18:31:10.45oai:repositorio.ufscar.br:ufscar/6220Repositório InstitucionalPUBhttps://repositorio.ufscar.br/oai/requestopendoar:43222023-09-18T18:31:10Repositório Institucional da UFSCAR - Universidade Federal de São Carlos (UFSCAR)false
dc.title.por.fl_str_mv Desenvolvimento e aplicação de biorreatores capilares para a triagem de ligantes de Purina Nucleosídeo Fosforilases
dc.title.alternative.eng.fl_str_mv Development and application of capillary bioreactors for screening of Purine Nucleoside Phosphorylases ligands
title Desenvolvimento e aplicação de biorreatores capilares para a triagem de ligantes de Purina Nucleosídeo Fosforilases
spellingShingle Desenvolvimento e aplicação de biorreatores capilares para a triagem de ligantes de Purina Nucleosídeo Fosforilases
Moraes, Marcela Cristina de
Química
Imobilização de enzimas
Ensaios enzimáticos
CIENCIAS EXATAS E DA TERRA::QUIMICA
title_short Desenvolvimento e aplicação de biorreatores capilares para a triagem de ligantes de Purina Nucleosídeo Fosforilases
title_full Desenvolvimento e aplicação de biorreatores capilares para a triagem de ligantes de Purina Nucleosídeo Fosforilases
title_fullStr Desenvolvimento e aplicação de biorreatores capilares para a triagem de ligantes de Purina Nucleosídeo Fosforilases
title_full_unstemmed Desenvolvimento e aplicação de biorreatores capilares para a triagem de ligantes de Purina Nucleosídeo Fosforilases
title_sort Desenvolvimento e aplicação de biorreatores capilares para a triagem de ligantes de Purina Nucleosídeo Fosforilases
author Moraes, Marcela Cristina de
author_facet Moraes, Marcela Cristina de
author_role author
dc.contributor.authorlattes.por.fl_str_mv http://lattes.cnpq.br/4092328724086308
dc.contributor.author.fl_str_mv Moraes, Marcela Cristina de
dc.contributor.advisor1.fl_str_mv Cass, Quezia Bezerra
dc.contributor.advisor1Lattes.fl_str_mv http://genos.cnpq.br:12010/dwlattes/owa/prc_imp_cv_int?f_cod=K4781559E6
dc.contributor.authorID.fl_str_mv 5653cb50-4b39-401a-bf1a-3708dbbec832
contributor_str_mv Cass, Quezia Bezerra
dc.subject.por.fl_str_mv Química
Imobilização de enzimas
Ensaios enzimáticos
topic Química
Imobilização de enzimas
Ensaios enzimáticos
CIENCIAS EXATAS E DA TERRA::QUIMICA
dc.subject.cnpq.fl_str_mv CIENCIAS EXATAS E DA TERRA::QUIMICA
description Purine Nucleoside Phosphorylases (PNPs) are key enzymes of the purine salvage pathway, and therefore are considered attractive targets for new drugs search. In this context, the development of effective and selective bioassays for PNP ligands screening is an important task. This work describes the covalent immobilization of human and Schistossoma mansoni PNP on fused silica capillaries. The activity of the immobilized enzyme reactors (IMERs) was monitored on line, employing multidimensional zonal chromatography, by the quantification of the product formed throughout the enzymatic reaction. This method enabled the determination of kinetic constants, screening, identification and characterization of enzymatic inhibitors. Two potent human PNP inhibitors were recognized and characterized. Through the use of inhibitors with different potencies, previously characterized by zonal chromatography, the affinity-based ligands screening employing frontal chromatography was validated. Frontal affinity chromatography analysis demonstrated to be a valuable method for the rapid identification of new ligands, while the main advantage of the multidimensional zonal chromatography method herein described consists on the ability to directly evaluate the effect of the ligands in the biological function of these enzymes. The methods described in this work represent an improvement to the PNPs inhibitors consolidated screening assays, since they directly quantify the enzymatic reaction product or are able to rank the inhibitors according to their affinities, resulting in a rapid automated analysis and false positives free.
publishDate 2012
dc.date.available.fl_str_mv 2012-03-19
2016-06-02T20:34:33Z
dc.date.issued.fl_str_mv 2012-02-28
dc.date.accessioned.fl_str_mv 2016-06-02T20:34:33Z
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dc.identifier.citation.fl_str_mv MORAES, Marcela Cristina de. Development and application of capillary bioreactors for screening of Purine Nucleoside Phosphorylases ligands. 2012. 150 f. Tese (Doutorado em Ciências Exatas e da Terra) - Universidade Federal de São Carlos, São Carlos, 2012.
dc.identifier.uri.fl_str_mv https://repositorio.ufscar.br/handle/ufscar/6220
identifier_str_mv MORAES, Marcela Cristina de. Development and application of capillary bioreactors for screening of Purine Nucleoside Phosphorylases ligands. 2012. 150 f. Tese (Doutorado em Ciências Exatas e da Terra) - Universidade Federal de São Carlos, São Carlos, 2012.
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