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Identification of a novel protein 3a from severe acute respiratory syndrome coronavirus
The open reading frame 3 of the severe acute respiratory syndrome coronavirus (SARS‐CoV) genome encodes a predicted protein 3a, consisting of 274 amino acids, that lacks any significant similarities to any known protein. We generated specific antibodies against SARS protein 3a by using a synthetic p...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2004
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126674/ https://www.ncbi.nlm.nih.gov/pubmed/15135062 http://dx.doi.org/10.1016/j.febslet.2004.03.086 |
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author | Yu, Chia-Jung Chen, Yee-Chun Hsiao, Cheng-Hsiang Kuo, Tse-Chun Chang, Shin C. Lu, Chun-Yi Wei, Wen-Chin Lee, Chia-Huei Huang, Li-Min Chang, Ming-Fu Ho, Hong-Nerng Lee, Fang-Jen S. |
author_facet | Yu, Chia-Jung Chen, Yee-Chun Hsiao, Cheng-Hsiang Kuo, Tse-Chun Chang, Shin C. Lu, Chun-Yi Wei, Wen-Chin Lee, Chia-Huei Huang, Li-Min Chang, Ming-Fu Ho, Hong-Nerng Lee, Fang-Jen S. |
author_sort | Yu, Chia-Jung |
collection | PubMed |
description | The open reading frame 3 of the severe acute respiratory syndrome coronavirus (SARS‐CoV) genome encodes a predicted protein 3a, consisting of 274 amino acids, that lacks any significant similarities to any known protein. We generated specific antibodies against SARS protein 3a by using a synthetic peptide (P2) corresponding to amino acids 261–274 of the putative protein. Anti‐P2 antibodies and the sera from SARS patients could specifically detect the recombinant SARS protein 3a expressed in Escherichia coli and in Vero E6 cells. Expression of SARS protein 3a was detected at 8–12 h after infection and reached a higher level after ∼24 h in SARS‐CoV‐infected Vero E6 cells. Protein 3a was also detected in the alveolar lining pneumocytes and some intra‐alveolar cells of a SARS‐CoV‐infected patient's lung specimen. Recombinant protein 3a expressed in Vero E6 cells and protein 3a in the SARS‐CoV‐infected cells was distributed over the cytoplasm in a fine punctate pattern with partly concentrated staining in the Golgi apparatus. Our study demonstrates that SARS‐CoV indeed expresses a novel protein 3a, which is present only in SARS‐CoV and not in other known CoVs. |
format | Online Article Text |
id | pubmed-7126674 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71266742020-04-08 Identification of a novel protein 3a from severe acute respiratory syndrome coronavirus Yu, Chia-Jung Chen, Yee-Chun Hsiao, Cheng-Hsiang Kuo, Tse-Chun Chang, Shin C. Lu, Chun-Yi Wei, Wen-Chin Lee, Chia-Huei Huang, Li-Min Chang, Ming-Fu Ho, Hong-Nerng Lee, Fang-Jen S. FEBS Lett Short Communications The open reading frame 3 of the severe acute respiratory syndrome coronavirus (SARS‐CoV) genome encodes a predicted protein 3a, consisting of 274 amino acids, that lacks any significant similarities to any known protein. We generated specific antibodies against SARS protein 3a by using a synthetic peptide (P2) corresponding to amino acids 261–274 of the putative protein. Anti‐P2 antibodies and the sera from SARS patients could specifically detect the recombinant SARS protein 3a expressed in Escherichia coli and in Vero E6 cells. Expression of SARS protein 3a was detected at 8–12 h after infection and reached a higher level after ∼24 h in SARS‐CoV‐infected Vero E6 cells. Protein 3a was also detected in the alveolar lining pneumocytes and some intra‐alveolar cells of a SARS‐CoV‐infected patient's lung specimen. Recombinant protein 3a expressed in Vero E6 cells and protein 3a in the SARS‐CoV‐infected cells was distributed over the cytoplasm in a fine punctate pattern with partly concentrated staining in the Golgi apparatus. Our study demonstrates that SARS‐CoV indeed expresses a novel protein 3a, which is present only in SARS‐CoV and not in other known CoVs. John Wiley and Sons Inc. 2004-05-07 2004-04-13 /pmc/articles/PMC7126674/ /pubmed/15135062 http://dx.doi.org/10.1016/j.febslet.2004.03.086 Text en FEBS Letters 565 (2004) 1873-3468 © 2015 Federation of European Biochemical Societies This article is being made freely available through PubMed Central as part of the COVID-19 public health emergency response. It can be used for unrestricted research re-use and analysis in any form or by any means with acknowledgement of the original source, for the duration of the public health emergency. |
spellingShingle | Short Communications Yu, Chia-Jung Chen, Yee-Chun Hsiao, Cheng-Hsiang Kuo, Tse-Chun Chang, Shin C. Lu, Chun-Yi Wei, Wen-Chin Lee, Chia-Huei Huang, Li-Min Chang, Ming-Fu Ho, Hong-Nerng Lee, Fang-Jen S. Identification of a novel protein 3a from severe acute respiratory syndrome coronavirus |
title | Identification of a novel protein 3a from severe acute respiratory syndrome coronavirus |
title_full | Identification of a novel protein 3a from severe acute respiratory syndrome coronavirus |
title_fullStr | Identification of a novel protein 3a from severe acute respiratory syndrome coronavirus |
title_full_unstemmed | Identification of a novel protein 3a from severe acute respiratory syndrome coronavirus |
title_short | Identification of a novel protein 3a from severe acute respiratory syndrome coronavirus |
title_sort | identification of a novel protein 3a from severe acute respiratory syndrome coronavirus |
topic | Short Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126674/ https://www.ncbi.nlm.nih.gov/pubmed/15135062 http://dx.doi.org/10.1016/j.febslet.2004.03.086 |
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