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Adenoviral E4 34K protein interacts with virus packaging components and may serve as the putative portal
Studies on dsDNA bacteriophages have revealed that a DNA packaging complex assembles at a special vertex called the ‘portal vertex’ and consists of a portal, a DNA packaging ATPase and other components. AdV protein IVa2 is presumed to function as a DNA packaging ATPase. However, a protein that funct...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5548797/ https://www.ncbi.nlm.nih.gov/pubmed/28790440 http://dx.doi.org/10.1038/s41598-017-07997-w |
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author | Ahi, Yadvinder S. Hassan, Ahmed O. Vemula, Sai V. Li, Kunpeng Jiang, Wen Zhang, Guang Jun Mittal, Suresh K. |
author_facet | Ahi, Yadvinder S. Hassan, Ahmed O. Vemula, Sai V. Li, Kunpeng Jiang, Wen Zhang, Guang Jun Mittal, Suresh K. |
author_sort | Ahi, Yadvinder S. |
collection | PubMed |
description | Studies on dsDNA bacteriophages have revealed that a DNA packaging complex assembles at a special vertex called the ‘portal vertex’ and consists of a portal, a DNA packaging ATPase and other components. AdV protein IVa2 is presumed to function as a DNA packaging ATPase. However, a protein that functions as a portal is not yet identified in AdVs. To identify the AdV portal, we performed secondary structure analysis on a set of AdV proteins and compared them with the clip region of the portal proteins of bacteriophages phi29, SPP1 and T4. Our analysis revealed that the E4 34K protein of HAdV-C5 contains a region of strong similarity with the clip region of the known portal proteins. E4 34K was found to be present in empty as well as mature AdV particles. In addition, E4 34K co-immunoprecipitates and colocalizes with AdV packaging proteins. Immunogold electron microscopy demonstrated that E4 34K is located at a single site on the virus surface. Finally, tertiary structure prediction of E4 34K and its comparison with that of single subunits of Phi29, SPP1 and T4 portal proteins revealed remarkable similarity. In conclusion, our results suggest that E4 34K is the putative AdV portal protein. |
format | Online Article Text |
id | pubmed-5548797 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55487972017-08-09 Adenoviral E4 34K protein interacts with virus packaging components and may serve as the putative portal Ahi, Yadvinder S. Hassan, Ahmed O. Vemula, Sai V. Li, Kunpeng Jiang, Wen Zhang, Guang Jun Mittal, Suresh K. Sci Rep Article Studies on dsDNA bacteriophages have revealed that a DNA packaging complex assembles at a special vertex called the ‘portal vertex’ and consists of a portal, a DNA packaging ATPase and other components. AdV protein IVa2 is presumed to function as a DNA packaging ATPase. However, a protein that functions as a portal is not yet identified in AdVs. To identify the AdV portal, we performed secondary structure analysis on a set of AdV proteins and compared them with the clip region of the portal proteins of bacteriophages phi29, SPP1 and T4. Our analysis revealed that the E4 34K protein of HAdV-C5 contains a region of strong similarity with the clip region of the known portal proteins. E4 34K was found to be present in empty as well as mature AdV particles. In addition, E4 34K co-immunoprecipitates and colocalizes with AdV packaging proteins. Immunogold electron microscopy demonstrated that E4 34K is located at a single site on the virus surface. Finally, tertiary structure prediction of E4 34K and its comparison with that of single subunits of Phi29, SPP1 and T4 portal proteins revealed remarkable similarity. In conclusion, our results suggest that E4 34K is the putative AdV portal protein. Nature Publishing Group UK 2017-08-08 /pmc/articles/PMC5548797/ /pubmed/28790440 http://dx.doi.org/10.1038/s41598-017-07997-w Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Ahi, Yadvinder S. Hassan, Ahmed O. Vemula, Sai V. Li, Kunpeng Jiang, Wen Zhang, Guang Jun Mittal, Suresh K. Adenoviral E4 34K protein interacts with virus packaging components and may serve as the putative portal |
title | Adenoviral E4 34K protein interacts with virus packaging components and may serve as the putative portal |
title_full | Adenoviral E4 34K protein interacts with virus packaging components and may serve as the putative portal |
title_fullStr | Adenoviral E4 34K protein interacts with virus packaging components and may serve as the putative portal |
title_full_unstemmed | Adenoviral E4 34K protein interacts with virus packaging components and may serve as the putative portal |
title_short | Adenoviral E4 34K protein interacts with virus packaging components and may serve as the putative portal |
title_sort | adenoviral e4 34k protein interacts with virus packaging components and may serve as the putative portal |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5548797/ https://www.ncbi.nlm.nih.gov/pubmed/28790440 http://dx.doi.org/10.1038/s41598-017-07997-w |
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