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CRISPR/dCas9-mediated biosensor for detection of tick-borne diseases
Rapid and highly sensitive detection of biomolecules is greatly needed for pathogen diagnosis in clinical samples, but the method needs to be significantly improved in terms of sensitivity and specificity for actual use in clinical settings. Here, we report the development of an improved molecular d...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126152/ https://www.ncbi.nlm.nih.gov/pubmed/32288252 http://dx.doi.org/10.1016/j.snb.2018.06.069 |
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author | Koo, Bonhan Kim, Da-eun Kweon, Jiyeon Jin, Choong Eun Kim, Sung-Han Kim, Yongsub Shin, Yong |
author_facet | Koo, Bonhan Kim, Da-eun Kweon, Jiyeon Jin, Choong Eun Kim, Sung-Han Kim, Yongsub Shin, Yong |
author_sort | Koo, Bonhan |
collection | PubMed |
description | Rapid and highly sensitive detection of biomolecules is greatly needed for pathogen diagnosis in clinical samples, but the method needs to be significantly improved in terms of sensitivity and specificity for actual use in clinical settings. Here, we report the development of an improved molecular diagnostics tool that utilizes CRISPR/dCas9-mediated biosensor that couples a nuclease inactivated Cas9 (dCas9) and single microring resonator biosensor, enables label-free and real-time detection of pathogenic DNA and RNA. We addressed the clinical utility of this CRISPR/dCas9-mediated biosensor in tick-borne illnesses including scrub typhus (ST) and severe fever with thrombocytopenia syndrome (SFTS), whose clinical presentations are too similar to be easily differentiated. By using CRISPR/dCas9-mediated biosensor, we achieved single molecule sensitivity for the detection of ST (0.54 aM) and SFTS (0.63 aM); this detection sensitivity is 100 times more sensitive than that of RT-PCR assay. Finally, CRISPR/dCas9-mediated biosensor was able to clearly distinguish between ST and SFTS in serum samples within 20 min. We believe that CRISPR/dCas9-mediated biosensor will be useful for rapid and accurate molecular diagnostic tool that is suitable for immediate clinical applications. |
format | Online Article Text |
id | pubmed-7126152 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71261522020-04-08 CRISPR/dCas9-mediated biosensor for detection of tick-borne diseases Koo, Bonhan Kim, Da-eun Kweon, Jiyeon Jin, Choong Eun Kim, Sung-Han Kim, Yongsub Shin, Yong Sens Actuators B Chem Article Rapid and highly sensitive detection of biomolecules is greatly needed for pathogen diagnosis in clinical samples, but the method needs to be significantly improved in terms of sensitivity and specificity for actual use in clinical settings. Here, we report the development of an improved molecular diagnostics tool that utilizes CRISPR/dCas9-mediated biosensor that couples a nuclease inactivated Cas9 (dCas9) and single microring resonator biosensor, enables label-free and real-time detection of pathogenic DNA and RNA. We addressed the clinical utility of this CRISPR/dCas9-mediated biosensor in tick-borne illnesses including scrub typhus (ST) and severe fever with thrombocytopenia syndrome (SFTS), whose clinical presentations are too similar to be easily differentiated. By using CRISPR/dCas9-mediated biosensor, we achieved single molecule sensitivity for the detection of ST (0.54 aM) and SFTS (0.63 aM); this detection sensitivity is 100 times more sensitive than that of RT-PCR assay. Finally, CRISPR/dCas9-mediated biosensor was able to clearly distinguish between ST and SFTS in serum samples within 20 min. We believe that CRISPR/dCas9-mediated biosensor will be useful for rapid and accurate molecular diagnostic tool that is suitable for immediate clinical applications. Elsevier B.V. 2018-11-10 2018-06-15 /pmc/articles/PMC7126152/ /pubmed/32288252 http://dx.doi.org/10.1016/j.snb.2018.06.069 Text en © 2018 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Koo, Bonhan Kim, Da-eun Kweon, Jiyeon Jin, Choong Eun Kim, Sung-Han Kim, Yongsub Shin, Yong CRISPR/dCas9-mediated biosensor for detection of tick-borne diseases |
title | CRISPR/dCas9-mediated biosensor for detection of tick-borne diseases |
title_full | CRISPR/dCas9-mediated biosensor for detection of tick-borne diseases |
title_fullStr | CRISPR/dCas9-mediated biosensor for detection of tick-borne diseases |
title_full_unstemmed | CRISPR/dCas9-mediated biosensor for detection of tick-borne diseases |
title_short | CRISPR/dCas9-mediated biosensor for detection of tick-borne diseases |
title_sort | crispr/dcas9-mediated biosensor for detection of tick-borne diseases |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126152/ https://www.ncbi.nlm.nih.gov/pubmed/32288252 http://dx.doi.org/10.1016/j.snb.2018.06.069 |
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