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All-fiber all-optical quantitative polymerase chain reaction (qPCR)
Quantitative polymerase chain reaction (qPCR), the real-time amplification and measurement of a targeted DNA molecule, has revolutionized the biological sciences and is routinely applied in areas such as medical diagnostics, forensics, and agriculture. Despite widescale use of qPCR technology in the...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7415342/ https://www.ncbi.nlm.nih.gov/pubmed/32834504 http://dx.doi.org/10.1016/j.snb.2020.128681 |
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author | Li, Xuegang Nguyen, Linh V. Hill, Kelly Ebendorff-Heidepriem, Heike Schartner, Erik P. Zhao, Yong Zhou, Xue Zhang, Yanan Warren-Smith, Stephen C. |
author_facet | Li, Xuegang Nguyen, Linh V. Hill, Kelly Ebendorff-Heidepriem, Heike Schartner, Erik P. Zhao, Yong Zhou, Xue Zhang, Yanan Warren-Smith, Stephen C. |
author_sort | Li, Xuegang |
collection | PubMed |
description | Quantitative polymerase chain reaction (qPCR), the real-time amplification and measurement of a targeted DNA molecule, has revolutionized the biological sciences and is routinely applied in areas such as medical diagnostics, forensics, and agriculture. Despite widescale use of qPCR technology in the lab, the availability of low-cost and high-speed portable systems remains one of the barriers to routine in-field implementation. Here we propose and demonstrate a potential solution using a photonics-based qPCR system. By using an all-optical approach, we achieve ultra-fast temperature response with real-time temperature feedback using nanoliter scale reaction volumes. The system uses a microcavity to act as a nanoliter scale reaction vessel with a laser-driven and optically monitored temperature cycling system for ultrafast thermal cycling and incorporates an all-fiber fluorescence excitation/detection system to achieve real-time, high sensitivity fluorescence monitoring of the qPCR process. Further, we demonstrate the potential of the system to operate as a label-free qPCR system through direct optical measurement of the sample refractive index. Due to advantages in portability and fabrication simplicity, we anticipate that this platform technology will offer a new strategy for fundamental techniques in biochemistry applications, such as point-of-care and remote diagnostics. |
format | Online Article Text |
id | pubmed-7415342 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74153422020-08-10 All-fiber all-optical quantitative polymerase chain reaction (qPCR) Li, Xuegang Nguyen, Linh V. Hill, Kelly Ebendorff-Heidepriem, Heike Schartner, Erik P. Zhao, Yong Zhou, Xue Zhang, Yanan Warren-Smith, Stephen C. Sens Actuators B Chem Article Quantitative polymerase chain reaction (qPCR), the real-time amplification and measurement of a targeted DNA molecule, has revolutionized the biological sciences and is routinely applied in areas such as medical diagnostics, forensics, and agriculture. Despite widescale use of qPCR technology in the lab, the availability of low-cost and high-speed portable systems remains one of the barriers to routine in-field implementation. Here we propose and demonstrate a potential solution using a photonics-based qPCR system. By using an all-optical approach, we achieve ultra-fast temperature response with real-time temperature feedback using nanoliter scale reaction volumes. The system uses a microcavity to act as a nanoliter scale reaction vessel with a laser-driven and optically monitored temperature cycling system for ultrafast thermal cycling and incorporates an all-fiber fluorescence excitation/detection system to achieve real-time, high sensitivity fluorescence monitoring of the qPCR process. Further, we demonstrate the potential of the system to operate as a label-free qPCR system through direct optical measurement of the sample refractive index. Due to advantages in portability and fabrication simplicity, we anticipate that this platform technology will offer a new strategy for fundamental techniques in biochemistry applications, such as point-of-care and remote diagnostics. Elsevier B.V. 2020-11-15 2020-08-09 /pmc/articles/PMC7415342/ /pubmed/32834504 http://dx.doi.org/10.1016/j.snb.2020.128681 Text en © 2020 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 Li, Xuegang Nguyen, Linh V. Hill, Kelly Ebendorff-Heidepriem, Heike Schartner, Erik P. Zhao, Yong Zhou, Xue Zhang, Yanan Warren-Smith, Stephen C. All-fiber all-optical quantitative polymerase chain reaction (qPCR) |
title | All-fiber all-optical quantitative polymerase chain reaction (qPCR) |
title_full | All-fiber all-optical quantitative polymerase chain reaction (qPCR) |
title_fullStr | All-fiber all-optical quantitative polymerase chain reaction (qPCR) |
title_full_unstemmed | All-fiber all-optical quantitative polymerase chain reaction (qPCR) |
title_short | All-fiber all-optical quantitative polymerase chain reaction (qPCR) |
title_sort | all-fiber all-optical quantitative polymerase chain reaction (qpcr) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7415342/ https://www.ncbi.nlm.nih.gov/pubmed/32834504 http://dx.doi.org/10.1016/j.snb.2020.128681 |
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