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Development of Chemiluminescent Lateral Flow Assay for the Detection of Nucleic Acids

Rapid, sensitive detection methods are of utmost importance for the identification of pathogens related to health and safety. Herein we report the development of a nucleic acid sequence-based lateral flow assay which achieves a low limit of detection using chemiluminescence. On-membrane enzymatic si...

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Detalles Bibliográficos
Autores principales: Wang, Yuhong, Fill, Catherine, Nugen, Sam R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4263543/
https://www.ncbi.nlm.nih.gov/pubmed/25585630
http://dx.doi.org/10.3390/bios2010032
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author Wang, Yuhong
Fill, Catherine
Nugen, Sam R.
author_facet Wang, Yuhong
Fill, Catherine
Nugen, Sam R.
author_sort Wang, Yuhong
collection PubMed
description Rapid, sensitive detection methods are of utmost importance for the identification of pathogens related to health and safety. Herein we report the development of a nucleic acid sequence-based lateral flow assay which achieves a low limit of detection using chemiluminescence. On-membrane enzymatic signal amplification is used to reduce the limit of detection to the sub-femtomol level. To demonstrate this assay, we detected synthetic nucleic acid sequences representative of Trypanosoma mRNA, the causative agent for African sleeping sickness, with relevance in human and animal health in sub-Saharan Africa. The intensity of the chemiluminescent signal was evaluated by using a charge-coupled device as well as a microtiter plate reader. We demonstrated that our lateral flow chemiluminescent assay has a very low limit of detection and is easy to use. The limit of detection was determined to be 0.5 fmols of nucleic acid target.
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spelling pubmed-42635432015-01-13 Development of Chemiluminescent Lateral Flow Assay for the Detection of Nucleic Acids Wang, Yuhong Fill, Catherine Nugen, Sam R. Biosensors (Basel) Article Rapid, sensitive detection methods are of utmost importance for the identification of pathogens related to health and safety. Herein we report the development of a nucleic acid sequence-based lateral flow assay which achieves a low limit of detection using chemiluminescence. On-membrane enzymatic signal amplification is used to reduce the limit of detection to the sub-femtomol level. To demonstrate this assay, we detected synthetic nucleic acid sequences representative of Trypanosoma mRNA, the causative agent for African sleeping sickness, with relevance in human and animal health in sub-Saharan Africa. The intensity of the chemiluminescent signal was evaluated by using a charge-coupled device as well as a microtiter plate reader. We demonstrated that our lateral flow chemiluminescent assay has a very low limit of detection and is easy to use. The limit of detection was determined to be 0.5 fmols of nucleic acid target. MDPI 2012-01-18 /pmc/articles/PMC4263543/ /pubmed/25585630 http://dx.doi.org/10.3390/bios2010032 Text en © 2012 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ 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 Article
Wang, Yuhong
Fill, Catherine
Nugen, Sam R.
Development of Chemiluminescent Lateral Flow Assay for the Detection of Nucleic Acids
title Development of Chemiluminescent Lateral Flow Assay for the Detection of Nucleic Acids
title_full Development of Chemiluminescent Lateral Flow Assay for the Detection of Nucleic Acids
title_fullStr Development of Chemiluminescent Lateral Flow Assay for the Detection of Nucleic Acids
title_full_unstemmed Development of Chemiluminescent Lateral Flow Assay for the Detection of Nucleic Acids
title_short Development of Chemiluminescent Lateral Flow Assay for the Detection of Nucleic Acids
title_sort development of chemiluminescent lateral flow assay for the detection of nucleic acids
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4263543/
https://www.ncbi.nlm.nih.gov/pubmed/25585630
http://dx.doi.org/10.3390/bios2010032
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