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Rapid genetic screening with high quality factor metasurfaces

Genetic analysis methods are foundational to advancing personalized medicine, accelerating disease diagnostics, and monitoring the health of organisms and ecosystems. Current nucleic acid technologies such as polymerase chain reaction (PCR) and next-generation sequencing (NGS) rely on sample amplifi...

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Autores principales: Hu, Jack, Safir, Fareeha, Chang, Kai, Dagli, Sahil, Balch, Halleh B., Abendroth, John M., Dixon, Jefferson, Moradifar, Parivash, Dolia, Varun, Sahoo, Malaya K., Pinsky, Benjamin A., Jeffrey, Stefanie S., Lawrence, Mark, Dionne, Jennifer A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10372074/
https://www.ncbi.nlm.nih.gov/pubmed/37495593
http://dx.doi.org/10.1038/s41467-023-39721-w
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author Hu, Jack
Safir, Fareeha
Chang, Kai
Dagli, Sahil
Balch, Halleh B.
Abendroth, John M.
Dixon, Jefferson
Moradifar, Parivash
Dolia, Varun
Sahoo, Malaya K.
Pinsky, Benjamin A.
Jeffrey, Stefanie S.
Lawrence, Mark
Dionne, Jennifer A.
author_facet Hu, Jack
Safir, Fareeha
Chang, Kai
Dagli, Sahil
Balch, Halleh B.
Abendroth, John M.
Dixon, Jefferson
Moradifar, Parivash
Dolia, Varun
Sahoo, Malaya K.
Pinsky, Benjamin A.
Jeffrey, Stefanie S.
Lawrence, Mark
Dionne, Jennifer A.
author_sort Hu, Jack
collection PubMed
description Genetic analysis methods are foundational to advancing personalized medicine, accelerating disease diagnostics, and monitoring the health of organisms and ecosystems. Current nucleic acid technologies such as polymerase chain reaction (PCR) and next-generation sequencing (NGS) rely on sample amplification and can suffer from inhibition. Here, we introduce a label-free genetic screening platform based on high quality (high-Q) factor silicon nanoantennas functionalized with nucleic acid fragments. Each high-Q nanoantenna exhibits average resonant quality factors of 2,200 in physiological buffer. We quantitatively detect two gene fragments, SARS-CoV-2 envelope (E) and open reading frame 1b (ORF1b), with high-specificity via DNA hybridization. We also demonstrate femtomolar sensitivity in buffer and nanomolar sensitivity in spiked nasopharyngeal eluates within 5 minutes. Nanoantennas are patterned at densities of 160,000 devices per cm(2), enabling future work on highly-multiplexed detection. Combined with advances in complex sample processing, our work provides a foundation for rapid, compact, and amplification-free molecular assays.
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spelling pubmed-103720742023-07-28 Rapid genetic screening with high quality factor metasurfaces Hu, Jack Safir, Fareeha Chang, Kai Dagli, Sahil Balch, Halleh B. Abendroth, John M. Dixon, Jefferson Moradifar, Parivash Dolia, Varun Sahoo, Malaya K. Pinsky, Benjamin A. Jeffrey, Stefanie S. Lawrence, Mark Dionne, Jennifer A. Nat Commun Article Genetic analysis methods are foundational to advancing personalized medicine, accelerating disease diagnostics, and monitoring the health of organisms and ecosystems. Current nucleic acid technologies such as polymerase chain reaction (PCR) and next-generation sequencing (NGS) rely on sample amplification and can suffer from inhibition. Here, we introduce a label-free genetic screening platform based on high quality (high-Q) factor silicon nanoantennas functionalized with nucleic acid fragments. Each high-Q nanoantenna exhibits average resonant quality factors of 2,200 in physiological buffer. We quantitatively detect two gene fragments, SARS-CoV-2 envelope (E) and open reading frame 1b (ORF1b), with high-specificity via DNA hybridization. We also demonstrate femtomolar sensitivity in buffer and nanomolar sensitivity in spiked nasopharyngeal eluates within 5 minutes. Nanoantennas are patterned at densities of 160,000 devices per cm(2), enabling future work on highly-multiplexed detection. Combined with advances in complex sample processing, our work provides a foundation for rapid, compact, and amplification-free molecular assays. Nature Publishing Group UK 2023-07-26 /pmc/articles/PMC10372074/ /pubmed/37495593 http://dx.doi.org/10.1038/s41467-023-39721-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Hu, Jack
Safir, Fareeha
Chang, Kai
Dagli, Sahil
Balch, Halleh B.
Abendroth, John M.
Dixon, Jefferson
Moradifar, Parivash
Dolia, Varun
Sahoo, Malaya K.
Pinsky, Benjamin A.
Jeffrey, Stefanie S.
Lawrence, Mark
Dionne, Jennifer A.
Rapid genetic screening with high quality factor metasurfaces
title Rapid genetic screening with high quality factor metasurfaces
title_full Rapid genetic screening with high quality factor metasurfaces
title_fullStr Rapid genetic screening with high quality factor metasurfaces
title_full_unstemmed Rapid genetic screening with high quality factor metasurfaces
title_short Rapid genetic screening with high quality factor metasurfaces
title_sort rapid genetic screening with high quality factor metasurfaces
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10372074/
https://www.ncbi.nlm.nih.gov/pubmed/37495593
http://dx.doi.org/10.1038/s41467-023-39721-w
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