Monoclonal antibody anti-AFB1: scale-up in vitro for biotools development

Detalhes bibliográficos
Autor(a) principal: Takabayashi, Cássia Reika
Data de Publicação: 2010
Outros Autores: Hayashi, Luciana, Oliveira, Tatiane Martins de, Fujii, Simone, Kemmelmeier, Carlos, Ono, Elisabete Yurie Sataque, Itano, Eiko Nakagawa, Kawamura, Osamu, Hirooka, Elisa Yoko
Tipo de documento: Artigo
Idioma: por
Título da fonte: Semina. Ciências Agrárias (Online)
Texto Completo: https://ojs.uel.br/revistas/uel/index.php/semagrarias/article/view/7598
Resumo: Aflatoxin B1 (AFB1) is a mycotoxin classified as group 1 (human carcinogen) by International Agency for Research on Cancer - IARC, causing hazardous contamination in a wide variety of food and feed, where the monitoring depends on precision and accuracy of analytical method. The culture of AFB1 specific monoclonal antibody (mAb) secreting hybridoma was performed for further development of immunochemical methods. The growth of hybridoma AF2 was carried out in RPMI medium + 15 % fetal bovine serum (FBS), as well as the same medium gradually amended with H-SFM medium (25, 50, 75 and 100 % H-SFM). The protein concentration in the culture supernatant ranged from 1.80 to 10.88 mg/mL. The culture amended with FBS-free synthetic H-SFM medium reached production of reagent with higher degree of purity and lower risk, in addition to lower protein content (2.29 mg/mL reached with 100 % H-SFM), which approaches the real content of pure mAb. The indirect competitive enzyme-linked immunosorbent assay (ic-ELISA) and SDS-polyacrylamide gel electrophoresis (SDS-PAGE) showed anti-AFB1 activity and IgG corresponding bands, respectively, indicating feasible application of mAb produced in 100, 75 and 50 % H-SFM for further use in the development of AFB1 detecting biotools. This mAb production can be an initial step that can supply the self-sufficient immune-reagent in the rapid diagnosis at national condition, which is essential in the food quality and safety.
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spelling Monoclonal antibody anti-AFB1: scale-up in vitro for biotools developmentAnticorpo monoclonal antiAFB1: produção in vitro visando desenvolvimento de bioferramentasMonoclonal antibodyHybridomaBiotoolAFBAnticorpo monclonalHibridomaBioferramentaAFB1Aflatoxin B1 (AFB1) is a mycotoxin classified as group 1 (human carcinogen) by International Agency for Research on Cancer - IARC, causing hazardous contamination in a wide variety of food and feed, where the monitoring depends on precision and accuracy of analytical method. The culture of AFB1 specific monoclonal antibody (mAb) secreting hybridoma was performed for further development of immunochemical methods. The growth of hybridoma AF2 was carried out in RPMI medium + 15 % fetal bovine serum (FBS), as well as the same medium gradually amended with H-SFM medium (25, 50, 75 and 100 % H-SFM). The protein concentration in the culture supernatant ranged from 1.80 to 10.88 mg/mL. The culture amended with FBS-free synthetic H-SFM medium reached production of reagent with higher degree of purity and lower risk, in addition to lower protein content (2.29 mg/mL reached with 100 % H-SFM), which approaches the real content of pure mAb. The indirect competitive enzyme-linked immunosorbent assay (ic-ELISA) and SDS-polyacrylamide gel electrophoresis (SDS-PAGE) showed anti-AFB1 activity and IgG corresponding bands, respectively, indicating feasible application of mAb produced in 100, 75 and 50 % H-SFM for further use in the development of AFB1 detecting biotools. This mAb production can be an initial step that can supply the self-sufficient immune-reagent in the rapid diagnosis at national condition, which is essential in the food quality and safety.Aflatoxina B1 (AFB1) é uma micotoxina classificada pela International Agency  for Research on Cancer - IARC no Grupo 1 (carcinógeno ao humano), responsável pelo perigo de contaminação em ampla variedade de alimento e ração, cujo monitoramento depende de metodologia analítica precisa e exata. O trabalho visou cultivo do hibridoma secretor de anticorpo monoclonal (AcM) específico para AFB1 visando desenvolvimento de métodos imunoquímicos. Hibridoma AF2 foi cultivado em meio RPMI + 15 % de soro fetal bovino (SFB), assim como o mesmo meio com adição gradual de meio H-SFM (25, 50, 75 e 100 % H-SFM). A concentração proteica obtida no sobrenadante de cultura variou de 1,80 a 10,88 mg/mL. A introdução de meio sintético H-SFM isento de SFB permitiu obtenção de reagente com maior pureza e menor perigo, já que cultivos com maior proporção de H-SFM apresentou menor teor proteico (2,29 mg/mL em 100 % de H-SFM), sendo este provavelmente próximo ao teor real de AcM puro. O ensaio imunoenzimático competitivo indireto (ic-ELISA) e eletroforese em gel de poliacrilamida com SDS (SDS-PAGE) demonstraram atividade antiAFB1 e bandas correspondentes ao IgG, respectivamente, indicando viabilidade da aplicação de AcM produzido em 100, 75 e 50 % H-SFM para o desenvolvimento de bioferramentas para detecção de AFB1. Esta produção de AcM abre perspectiva perante autossuficiência de reagentes essenciais no diagnóstico rápido em condição nacional, contribuindo na qualidade e segurança de alimentos.UEL2010-12-20info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://ojs.uel.br/revistas/uel/index.php/semagrarias/article/view/759810.5433/1679-0359.2010v31n4p933Semina: Ciências Agrárias; Vol. 31 No. 4 (2010); 933-944Semina: Ciências Agrárias; v. 31 n. 4 (2010); 933-9441679-03591676-546Xreponame:Semina. Ciências Agrárias (Online)instname:Universidade Estadual de Londrina (UEL)instacron:UELporhttps://ojs.uel.br/revistas/uel/index.php/semagrarias/article/view/7598/6689Takabayashi, Cássia ReikaHayashi, LucianaOliveira, Tatiane Martins deFujii, SimoneKemmelmeier, CarlosOno, Elisabete Yurie SataqueItano, Eiko NakagawaKawamura, OsamuHirooka, Elisa Yokoinfo:eu-repo/semantics/openAccess2015-11-19T18:38:18Zoai:ojs.pkp.sfu.ca:article/7598Revistahttp://www.uel.br/revistas/uel/index.php/semagrariasPUBhttps://ojs.uel.br/revistas/uel/index.php/semagrarias/oaisemina.agrarias@uel.br1679-03591676-546Xopendoar:2015-11-19T18:38:18Semina. Ciências Agrárias (Online) - Universidade Estadual de Londrina (UEL)false
dc.title.none.fl_str_mv Monoclonal antibody anti-AFB1: scale-up in vitro for biotools development
Anticorpo monoclonal antiAFB1: produção in vitro visando desenvolvimento de bioferramentas
title Monoclonal antibody anti-AFB1: scale-up in vitro for biotools development
spellingShingle Monoclonal antibody anti-AFB1: scale-up in vitro for biotools development
Takabayashi, Cássia Reika
Monoclonal antibody
Hybridoma
Biotool
AFB
Anticorpo monclonal
Hibridoma
Bioferramenta
AFB1
title_short Monoclonal antibody anti-AFB1: scale-up in vitro for biotools development
title_full Monoclonal antibody anti-AFB1: scale-up in vitro for biotools development
title_fullStr Monoclonal antibody anti-AFB1: scale-up in vitro for biotools development
title_full_unstemmed Monoclonal antibody anti-AFB1: scale-up in vitro for biotools development
title_sort Monoclonal antibody anti-AFB1: scale-up in vitro for biotools development
author Takabayashi, Cássia Reika
author_facet Takabayashi, Cássia Reika
Hayashi, Luciana
Oliveira, Tatiane Martins de
Fujii, Simone
Kemmelmeier, Carlos
Ono, Elisabete Yurie Sataque
Itano, Eiko Nakagawa
Kawamura, Osamu
Hirooka, Elisa Yoko
author_role author
author2 Hayashi, Luciana
Oliveira, Tatiane Martins de
Fujii, Simone
Kemmelmeier, Carlos
Ono, Elisabete Yurie Sataque
Itano, Eiko Nakagawa
Kawamura, Osamu
Hirooka, Elisa Yoko
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Takabayashi, Cássia Reika
Hayashi, Luciana
Oliveira, Tatiane Martins de
Fujii, Simone
Kemmelmeier, Carlos
Ono, Elisabete Yurie Sataque
Itano, Eiko Nakagawa
Kawamura, Osamu
Hirooka, Elisa Yoko
dc.subject.por.fl_str_mv Monoclonal antibody
Hybridoma
Biotool
AFB
Anticorpo monclonal
Hibridoma
Bioferramenta
AFB1
topic Monoclonal antibody
Hybridoma
Biotool
AFB
Anticorpo monclonal
Hibridoma
Bioferramenta
AFB1
description Aflatoxin B1 (AFB1) is a mycotoxin classified as group 1 (human carcinogen) by International Agency for Research on Cancer - IARC, causing hazardous contamination in a wide variety of food and feed, where the monitoring depends on precision and accuracy of analytical method. The culture of AFB1 specific monoclonal antibody (mAb) secreting hybridoma was performed for further development of immunochemical methods. The growth of hybridoma AF2 was carried out in RPMI medium + 15 % fetal bovine serum (FBS), as well as the same medium gradually amended with H-SFM medium (25, 50, 75 and 100 % H-SFM). The protein concentration in the culture supernatant ranged from 1.80 to 10.88 mg/mL. The culture amended with FBS-free synthetic H-SFM medium reached production of reagent with higher degree of purity and lower risk, in addition to lower protein content (2.29 mg/mL reached with 100 % H-SFM), which approaches the real content of pure mAb. The indirect competitive enzyme-linked immunosorbent assay (ic-ELISA) and SDS-polyacrylamide gel electrophoresis (SDS-PAGE) showed anti-AFB1 activity and IgG corresponding bands, respectively, indicating feasible application of mAb produced in 100, 75 and 50 % H-SFM for further use in the development of AFB1 detecting biotools. This mAb production can be an initial step that can supply the self-sufficient immune-reagent in the rapid diagnosis at national condition, which is essential in the food quality and safety.
publishDate 2010
dc.date.none.fl_str_mv 2010-12-20
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://ojs.uel.br/revistas/uel/index.php/semagrarias/article/view/7598
10.5433/1679-0359.2010v31n4p933
url https://ojs.uel.br/revistas/uel/index.php/semagrarias/article/view/7598
identifier_str_mv 10.5433/1679-0359.2010v31n4p933
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv https://ojs.uel.br/revistas/uel/index.php/semagrarias/article/view/7598/6689
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv UEL
publisher.none.fl_str_mv UEL
dc.source.none.fl_str_mv Semina: Ciências Agrárias; Vol. 31 No. 4 (2010); 933-944
Semina: Ciências Agrárias; v. 31 n. 4 (2010); 933-944
1679-0359
1676-546X
reponame:Semina. Ciências Agrárias (Online)
instname:Universidade Estadual de Londrina (UEL)
instacron:UEL
instname_str Universidade Estadual de Londrina (UEL)
instacron_str UEL
institution UEL
reponame_str Semina. Ciências Agrárias (Online)
collection Semina. Ciências Agrárias (Online)
repository.name.fl_str_mv Semina. Ciências Agrárias (Online) - Universidade Estadual de Londrina (UEL)
repository.mail.fl_str_mv semina.agrarias@uel.br
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