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Bio-SCAN V2: A CRISPR/dCas9-based lateral flow assay for rapid detection of theophylline
Rapid, specific, and robust diagnostic strategies are needed to develop sensitive biosensors for small molecule detection, which could aid in controlling contamination and disease transmission. Recently, the target-induced collateral activity of Cas nucleases [clustered regularly interspaced short p...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9893010/ https://www.ncbi.nlm.nih.gov/pubmed/36741753 http://dx.doi.org/10.3389/fbioe.2023.1118684 |
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author | Jiang, Wenjun Aman, Rashid Ali, Zahir Mahfouz, Magdy |
author_facet | Jiang, Wenjun Aman, Rashid Ali, Zahir Mahfouz, Magdy |
author_sort | Jiang, Wenjun |
collection | PubMed |
description | Rapid, specific, and robust diagnostic strategies are needed to develop sensitive biosensors for small molecule detection, which could aid in controlling contamination and disease transmission. Recently, the target-induced collateral activity of Cas nucleases [clustered regularly interspaced short palindromic repeats (CRISPR)-associated nucleases] was exploited to develop high-throughput diagnostic modules for detecting nucleic acids and small molecules. Here, we have expanded the diagnostic ability of the CRISPR-Cas system by developing Bio-SCAN V2, a ligand-responsive CRISPR-Cas platform for detecting non-nucleic acid small molecule targets. The Bio-SCAN V2 consists of an engineered ligand-responsive sgRNA (ligRNA), biotinylated dead Cas9 (dCas9-biotin), 6-carboxyfluorescein (FAM)-labeled amplicons, and lateral flow assay (LFA) strips. LigRNA interacts with dCas9-biotin only in the presence of sgRNA-specific ligand molecules to make a ribonucleoprotein (RNP). Next, the ligand-induced ribonucleoprotein is exposed to FAM-labeled amplicons for binding, and the presence of the ligand (small molecule) is detected as a visual signal [(dCas9-biotin)-ligRNA-FAM labeled DNA-AuNP complex] at the test line of the lateral flow assay strip. With the Bio-SCAN V2 platform, we are able to detect the model molecule theophylline with a limit of detection (LOD) up to 2 μM in a short time, requiring only 15 min from sample application to visual readout. Taken together, Bio-SCAN V2 assay provides a rapid, specific, and ultrasensitive detection platform for theophylline. |
format | Online Article Text |
id | pubmed-9893010 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98930102023-02-03 Bio-SCAN V2: A CRISPR/dCas9-based lateral flow assay for rapid detection of theophylline Jiang, Wenjun Aman, Rashid Ali, Zahir Mahfouz, Magdy Front Bioeng Biotechnol Bioengineering and Biotechnology Rapid, specific, and robust diagnostic strategies are needed to develop sensitive biosensors for small molecule detection, which could aid in controlling contamination and disease transmission. Recently, the target-induced collateral activity of Cas nucleases [clustered regularly interspaced short palindromic repeats (CRISPR)-associated nucleases] was exploited to develop high-throughput diagnostic modules for detecting nucleic acids and small molecules. Here, we have expanded the diagnostic ability of the CRISPR-Cas system by developing Bio-SCAN V2, a ligand-responsive CRISPR-Cas platform for detecting non-nucleic acid small molecule targets. The Bio-SCAN V2 consists of an engineered ligand-responsive sgRNA (ligRNA), biotinylated dead Cas9 (dCas9-biotin), 6-carboxyfluorescein (FAM)-labeled amplicons, and lateral flow assay (LFA) strips. LigRNA interacts with dCas9-biotin only in the presence of sgRNA-specific ligand molecules to make a ribonucleoprotein (RNP). Next, the ligand-induced ribonucleoprotein is exposed to FAM-labeled amplicons for binding, and the presence of the ligand (small molecule) is detected as a visual signal [(dCas9-biotin)-ligRNA-FAM labeled DNA-AuNP complex] at the test line of the lateral flow assay strip. With the Bio-SCAN V2 platform, we are able to detect the model molecule theophylline with a limit of detection (LOD) up to 2 μM in a short time, requiring only 15 min from sample application to visual readout. Taken together, Bio-SCAN V2 assay provides a rapid, specific, and ultrasensitive detection platform for theophylline. Frontiers Media S.A. 2023-01-19 /pmc/articles/PMC9893010/ /pubmed/36741753 http://dx.doi.org/10.3389/fbioe.2023.1118684 Text en Copyright © 2023 Jiang, Aman, Ali and Mahfouz. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Bioengineering and Biotechnology Jiang, Wenjun Aman, Rashid Ali, Zahir Mahfouz, Magdy Bio-SCAN V2: A CRISPR/dCas9-based lateral flow assay for rapid detection of theophylline |
title | Bio-SCAN V2: A CRISPR/dCas9-based lateral flow assay for rapid detection of theophylline |
title_full | Bio-SCAN V2: A CRISPR/dCas9-based lateral flow assay for rapid detection of theophylline |
title_fullStr | Bio-SCAN V2: A CRISPR/dCas9-based lateral flow assay for rapid detection of theophylline |
title_full_unstemmed | Bio-SCAN V2: A CRISPR/dCas9-based lateral flow assay for rapid detection of theophylline |
title_short | Bio-SCAN V2: A CRISPR/dCas9-based lateral flow assay for rapid detection of theophylline |
title_sort | bio-scan v2: a crispr/dcas9-based lateral flow assay for rapid detection of theophylline |
topic | Bioengineering and Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9893010/ https://www.ncbi.nlm.nih.gov/pubmed/36741753 http://dx.doi.org/10.3389/fbioe.2023.1118684 |
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