Monoclonal antibody anti-AFB1: scale-up in vitro for biotools development
Autor(a) principal: | |
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Data de Publicação: | 2010 |
Outros Autores: | , , , , , , , |
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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Semina. Ciências Agrárias (Online) |
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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 |
_version_ |
1799306064359849984 |