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A Recombinant Multiepitope Protein for Hepatitis B Diagnosis

Hepatitis B is a liver inflammation caused by hepatitis B virus (HBV) and can be diagnosed in clinical stage by hepatitis B core antibody from IgM class (anti-HBcIgM). Hepatitis B core antibody from IgG class (Anti-HBcIgG) appears quickly after IgM, reaching high titers in chronic hepatitis, and rem...

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Autores principales: de Souza, Marilen Queiroz, Galdino, Alexsandro Sobreira, dos Santos, José Carlos, Soares, Marcus Vinicius, de Nóbrega, Yanna C., Álvares, Alice da Cunha Morales, de Freitas, Sonia Maria, Torres, Fernando Araripe Gonçalves, Felipe, Maria Sueli Soares
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3835477/
https://www.ncbi.nlm.nih.gov/pubmed/24294596
http://dx.doi.org/10.1155/2013/148317
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author de Souza, Marilen Queiroz
Galdino, Alexsandro Sobreira
dos Santos, José Carlos
Soares, Marcus Vinicius
de Nóbrega, Yanna C.
Álvares, Alice da Cunha Morales
de Freitas, Sonia Maria
Torres, Fernando Araripe Gonçalves
Felipe, Maria Sueli Soares
author_facet de Souza, Marilen Queiroz
Galdino, Alexsandro Sobreira
dos Santos, José Carlos
Soares, Marcus Vinicius
de Nóbrega, Yanna C.
Álvares, Alice da Cunha Morales
de Freitas, Sonia Maria
Torres, Fernando Araripe Gonçalves
Felipe, Maria Sueli Soares
author_sort de Souza, Marilen Queiroz
collection PubMed
description Hepatitis B is a liver inflammation caused by hepatitis B virus (HBV) and can be diagnosed in clinical stage by hepatitis B core antibody from IgM class (anti-HBcIgM). Hepatitis B core antibody from IgG class (Anti-HBcIgG) appears quickly after IgM, reaching high titers in chronic hepatitis, and remains even after cure. Since hepatitis B core antibody (anti-HBc) is the first antibody identified and sometimes the only marker detected during the course of infection, it can be used both to indicate HBV acute infection (anti-HBc-IgM) and to identify individuals who have come into contact with the virus (anti-HBc-IgG). In this work we propose a recombinant hepatitis B core multiepitope antigen (rMEHB) to be used for diagnosis of hepatitis B. For this purpose, a synthetic gene coding for rMEHB was designed and cloned into vector pET21a with a 6xHis tag at the C-terminal. Time course induction in E. coli showed an induced protein with an apparent molecular mass of ~21 kDa. Protein purification was performed by a single step with affinity chromatography Ni-NTA. Circular dichroism spectroscopy indicated rMEHB as a thermal stable protein at pH 7.0 and 8.0. In these conditions rMEHB was successfully used to perform an enzyme linked immuno sorbent assay (ELISA) with positive and negative sera.
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spelling pubmed-38354772013-12-01 A Recombinant Multiepitope Protein for Hepatitis B Diagnosis de Souza, Marilen Queiroz Galdino, Alexsandro Sobreira dos Santos, José Carlos Soares, Marcus Vinicius de Nóbrega, Yanna C. Álvares, Alice da Cunha Morales de Freitas, Sonia Maria Torres, Fernando Araripe Gonçalves Felipe, Maria Sueli Soares Biomed Res Int Research Article Hepatitis B is a liver inflammation caused by hepatitis B virus (HBV) and can be diagnosed in clinical stage by hepatitis B core antibody from IgM class (anti-HBcIgM). Hepatitis B core antibody from IgG class (Anti-HBcIgG) appears quickly after IgM, reaching high titers in chronic hepatitis, and remains even after cure. Since hepatitis B core antibody (anti-HBc) is the first antibody identified and sometimes the only marker detected during the course of infection, it can be used both to indicate HBV acute infection (anti-HBc-IgM) and to identify individuals who have come into contact with the virus (anti-HBc-IgG). In this work we propose a recombinant hepatitis B core multiepitope antigen (rMEHB) to be used for diagnosis of hepatitis B. For this purpose, a synthetic gene coding for rMEHB was designed and cloned into vector pET21a with a 6xHis tag at the C-terminal. Time course induction in E. coli showed an induced protein with an apparent molecular mass of ~21 kDa. Protein purification was performed by a single step with affinity chromatography Ni-NTA. Circular dichroism spectroscopy indicated rMEHB as a thermal stable protein at pH 7.0 and 8.0. In these conditions rMEHB was successfully used to perform an enzyme linked immuno sorbent assay (ELISA) with positive and negative sera. Hindawi Publishing Corporation 2013 2013-11-05 /pmc/articles/PMC3835477/ /pubmed/24294596 http://dx.doi.org/10.1155/2013/148317 Text en Copyright © 2013 Marilen Queiroz de Souza et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
de Souza, Marilen Queiroz
Galdino, Alexsandro Sobreira
dos Santos, José Carlos
Soares, Marcus Vinicius
de Nóbrega, Yanna C.
Álvares, Alice da Cunha Morales
de Freitas, Sonia Maria
Torres, Fernando Araripe Gonçalves
Felipe, Maria Sueli Soares
A Recombinant Multiepitope Protein for Hepatitis B Diagnosis
title A Recombinant Multiepitope Protein for Hepatitis B Diagnosis
title_full A Recombinant Multiepitope Protein for Hepatitis B Diagnosis
title_fullStr A Recombinant Multiepitope Protein for Hepatitis B Diagnosis
title_full_unstemmed A Recombinant Multiepitope Protein for Hepatitis B Diagnosis
title_short A Recombinant Multiepitope Protein for Hepatitis B Diagnosis
title_sort recombinant multiepitope protein for hepatitis b diagnosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3835477/
https://www.ncbi.nlm.nih.gov/pubmed/24294596
http://dx.doi.org/10.1155/2013/148317
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