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The Adenovirus Genome Contributes to the Structural Stability of the Virion

Adenovirus (Ad) vectors are currently the most commonly used platform for therapeutic gene delivery in human gene therapy clinical trials. Although these vectors are effective, many researchers seek to further improve the safety and efficacy of Ad-based vectors through detailed characterization of b...

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Autores principales: Saha, Bratati, Wong, Carmen M., Parks, Robin J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4189039/
https://www.ncbi.nlm.nih.gov/pubmed/25254384
http://dx.doi.org/10.3390/v6093563
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author Saha, Bratati
Wong, Carmen M.
Parks, Robin J.
author_facet Saha, Bratati
Wong, Carmen M.
Parks, Robin J.
author_sort Saha, Bratati
collection PubMed
description Adenovirus (Ad) vectors are currently the most commonly used platform for therapeutic gene delivery in human gene therapy clinical trials. Although these vectors are effective, many researchers seek to further improve the safety and efficacy of Ad-based vectors through detailed characterization of basic Ad biology relevant to its function as a vector system. Most Ad vectors are deleted of key, or all, viral protein coding sequences, which functions to not only prevent virus replication but also increase the cloning capacity of the vector for foreign DNA. However, radical modifications to the genome size significantly decreases virion stability, suggesting that the virus genome plays a role in maintaining the physical stability of the Ad virion. Indeed, a similar relationship between genome size and virion stability has been noted for many viruses. This review discusses the impact of the genome size on Ad virion stability and emphasizes the need to consider this aspect of virus biology in Ad-based vector design.
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spelling pubmed-41890392014-10-08 The Adenovirus Genome Contributes to the Structural Stability of the Virion Saha, Bratati Wong, Carmen M. Parks, Robin J. Viruses Review Adenovirus (Ad) vectors are currently the most commonly used platform for therapeutic gene delivery in human gene therapy clinical trials. Although these vectors are effective, many researchers seek to further improve the safety and efficacy of Ad-based vectors through detailed characterization of basic Ad biology relevant to its function as a vector system. Most Ad vectors are deleted of key, or all, viral protein coding sequences, which functions to not only prevent virus replication but also increase the cloning capacity of the vector for foreign DNA. However, radical modifications to the genome size significantly decreases virion stability, suggesting that the virus genome plays a role in maintaining the physical stability of the Ad virion. Indeed, a similar relationship between genome size and virion stability has been noted for many viruses. This review discusses the impact of the genome size on Ad virion stability and emphasizes the need to consider this aspect of virus biology in Ad-based vector design. MDPI 2014-09-24 /pmc/articles/PMC4189039/ /pubmed/25254384 http://dx.doi.org/10.3390/v6093563 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Saha, Bratati
Wong, Carmen M.
Parks, Robin J.
The Adenovirus Genome Contributes to the Structural Stability of the Virion
title The Adenovirus Genome Contributes to the Structural Stability of the Virion
title_full The Adenovirus Genome Contributes to the Structural Stability of the Virion
title_fullStr The Adenovirus Genome Contributes to the Structural Stability of the Virion
title_full_unstemmed The Adenovirus Genome Contributes to the Structural Stability of the Virion
title_short The Adenovirus Genome Contributes to the Structural Stability of the Virion
title_sort adenovirus genome contributes to the structural stability of the virion
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4189039/
https://www.ncbi.nlm.nih.gov/pubmed/25254384
http://dx.doi.org/10.3390/v6093563
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