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Universal Real-Time PCR-Based Assay for Lentiviral Titration

Lentiviral vectors are efficient vehicles for stable gene transfer in both dividing and non-dividing cells. This feature among others makes lentiviral vectors a powerful tool in molecular research. However, the use of lentiviruses in research studies and clinical trials requires a precise and valida...

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Autores principales: Barczak, Wojciech, Suchorska, Wiktoria, Rubiś, Błażej, Kulcenty, Katarzyna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4298670/
https://www.ncbi.nlm.nih.gov/pubmed/25370825
http://dx.doi.org/10.1007/s12033-014-9815-4
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author Barczak, Wojciech
Suchorska, Wiktoria
Rubiś, Błażej
Kulcenty, Katarzyna
author_facet Barczak, Wojciech
Suchorska, Wiktoria
Rubiś, Błażej
Kulcenty, Katarzyna
author_sort Barczak, Wojciech
collection PubMed
description Lentiviral vectors are efficient vehicles for stable gene transfer in both dividing and non-dividing cells. This feature among others makes lentiviral vectors a powerful tool in molecular research. However, the use of lentiviruses in research studies and clinical trials requires a precise and validated titration method. In this study, we describe a qPCR-based approach for estimation of lentiviral vector titer (pLV-THM-GFP). The use of WPRE (Woodchuck Hepatitis Virus Posttranscriptional Regulatory Element) and albumin genes as templates for an SYBR green-based real-time qPCR method allows for a rapid, sensitive, reproducible, and accurate assessment of lentiviral copy number at an integrated lentiviral DNA level. Furthermore, this optimization enables measurement of lentiviral concentration even in very poor quality and small quantity material. Consequently, this approach provides researchers with a tool to perform low-cost assessment with highly repeatable results.
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spelling pubmed-42986702015-01-23 Universal Real-Time PCR-Based Assay for Lentiviral Titration Barczak, Wojciech Suchorska, Wiktoria Rubiś, Błażej Kulcenty, Katarzyna Mol Biotechnol Research Lentiviral vectors are efficient vehicles for stable gene transfer in both dividing and non-dividing cells. This feature among others makes lentiviral vectors a powerful tool in molecular research. However, the use of lentiviruses in research studies and clinical trials requires a precise and validated titration method. In this study, we describe a qPCR-based approach for estimation of lentiviral vector titer (pLV-THM-GFP). The use of WPRE (Woodchuck Hepatitis Virus Posttranscriptional Regulatory Element) and albumin genes as templates for an SYBR green-based real-time qPCR method allows for a rapid, sensitive, reproducible, and accurate assessment of lentiviral copy number at an integrated lentiviral DNA level. Furthermore, this optimization enables measurement of lentiviral concentration even in very poor quality and small quantity material. Consequently, this approach provides researchers with a tool to perform low-cost assessment with highly repeatable results. Springer US 2014-11-05 2015 /pmc/articles/PMC4298670/ /pubmed/25370825 http://dx.doi.org/10.1007/s12033-014-9815-4 Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/4.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Research
Barczak, Wojciech
Suchorska, Wiktoria
Rubiś, Błażej
Kulcenty, Katarzyna
Universal Real-Time PCR-Based Assay for Lentiviral Titration
title Universal Real-Time PCR-Based Assay for Lentiviral Titration
title_full Universal Real-Time PCR-Based Assay for Lentiviral Titration
title_fullStr Universal Real-Time PCR-Based Assay for Lentiviral Titration
title_full_unstemmed Universal Real-Time PCR-Based Assay for Lentiviral Titration
title_short Universal Real-Time PCR-Based Assay for Lentiviral Titration
title_sort universal real-time pcr-based assay for lentiviral titration
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4298670/
https://www.ncbi.nlm.nih.gov/pubmed/25370825
http://dx.doi.org/10.1007/s12033-014-9815-4
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