Fluorescently Labeled Adenovirus with pIX-EGFP for Vector Detection

Adenoviruses are extensively studied in terms of their use as gene therapy vectors and pathogenesis. These vectors have been targeted on both transcriptional and transductional levels to achieve cell-specific gene delivery. Current detection strategies, including reporter gene expression, viral comp...

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Main Authors: Long P. Le, Maaike Everts, Igor P. Dmitriev, Julia G. Davydova, Masato Yamamoto, David T. Curiel
Format: Article
Language:English
Published: Hindawi - SAGE Publishing 2004-04-01
Series:Molecular Imaging
Online Access:https://doi.org/10.1162/15353500200404100
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spelling doaj-f59de83c4cb34af9b2f832cd2b44a0102021-04-02T11:25:10ZengHindawi - SAGE PublishingMolecular Imaging1536-01212004-04-01310.1162/1535350020040410010.1162_15353500200404100Fluorescently Labeled Adenovirus with pIX-EGFP for Vector DetectionLong P. LeMaaike EvertsIgor P. DmitrievJulia G. DavydovaMasato YamamotoDavid T. CurielAdenoviruses are extensively studied in terms of their use as gene therapy vectors and pathogenesis. These vectors have been targeted on both transcriptional and transductional levels to achieve cell-specific gene delivery. Current detection strategies, including reporter gene expression, viral component detection, and vector labeling with fluorophores, have been applied to analyze adenoviral vectors; however, these methods are inadequate for assessing transductional targeting. As an alternative to conventional vector detection techniques, we developed a specific genetic labeling system whereby an adenoviral vector incorporates a fusion between capsid protein IX and EGFP. DNA packaging and thermostability were marginally hampered by the modification while DNA replication, cytopathic effect, and CAR-dependent binding were not affected. The fluorescent label was associated with the virus capsid and conferred a fluorescent property useful in detecting adenoviral particles in flow cytometry, tracking, and tissue sections. We believe our genetic adenovirus labeling system has important implications for vector development, detecting adenovirus vectors in targeting schemes, and studying adenovirus biology. In addition, this technique has potential utility for dynamic monitoring of adenovirus replication and spread.https://doi.org/10.1162/15353500200404100
collection DOAJ
language English
format Article
sources DOAJ
author Long P. Le
Maaike Everts
Igor P. Dmitriev
Julia G. Davydova
Masato Yamamoto
David T. Curiel
spellingShingle Long P. Le
Maaike Everts
Igor P. Dmitriev
Julia G. Davydova
Masato Yamamoto
David T. Curiel
Fluorescently Labeled Adenovirus with pIX-EGFP for Vector Detection
Molecular Imaging
author_facet Long P. Le
Maaike Everts
Igor P. Dmitriev
Julia G. Davydova
Masato Yamamoto
David T. Curiel
author_sort Long P. Le
title Fluorescently Labeled Adenovirus with pIX-EGFP for Vector Detection
title_short Fluorescently Labeled Adenovirus with pIX-EGFP for Vector Detection
title_full Fluorescently Labeled Adenovirus with pIX-EGFP for Vector Detection
title_fullStr Fluorescently Labeled Adenovirus with pIX-EGFP for Vector Detection
title_full_unstemmed Fluorescently Labeled Adenovirus with pIX-EGFP for Vector Detection
title_sort fluorescently labeled adenovirus with pix-egfp for vector detection
publisher Hindawi - SAGE Publishing
series Molecular Imaging
issn 1536-0121
publishDate 2004-04-01
description Adenoviruses are extensively studied in terms of their use as gene therapy vectors and pathogenesis. These vectors have been targeted on both transcriptional and transductional levels to achieve cell-specific gene delivery. Current detection strategies, including reporter gene expression, viral component detection, and vector labeling with fluorophores, have been applied to analyze adenoviral vectors; however, these methods are inadequate for assessing transductional targeting. As an alternative to conventional vector detection techniques, we developed a specific genetic labeling system whereby an adenoviral vector incorporates a fusion between capsid protein IX and EGFP. DNA packaging and thermostability were marginally hampered by the modification while DNA replication, cytopathic effect, and CAR-dependent binding were not affected. The fluorescent label was associated with the virus capsid and conferred a fluorescent property useful in detecting adenoviral particles in flow cytometry, tracking, and tissue sections. We believe our genetic adenovirus labeling system has important implications for vector development, detecting adenovirus vectors in targeting schemes, and studying adenovirus biology. In addition, this technique has potential utility for dynamic monitoring of adenovirus replication and spread.
url https://doi.org/10.1162/15353500200404100
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