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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
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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. |
format | Online Article Text |
id | pubmed-3835477 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
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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