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Common-path interferometric label-free protein sensing with resonant dielectric nanostructures

Research toward photonic biosensors for point-of-care applications and personalized medicine is driven by the need for high-sensitivity, low-cost, and reliable technology. Among the most sensitive modalities, interferometry offers particularly high performance, but typically lacks the required opera...

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Autores principales: Barth, Isabel, Conteduca, Donato, Reardon, Christopher, Johnson, Steven, Krauss, Thomas F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7264974/
https://www.ncbi.nlm.nih.gov/pubmed/32509300
http://dx.doi.org/10.1038/s41377-020-0336-6
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author Barth, Isabel
Conteduca, Donato
Reardon, Christopher
Johnson, Steven
Krauss, Thomas F.
author_facet Barth, Isabel
Conteduca, Donato
Reardon, Christopher
Johnson, Steven
Krauss, Thomas F.
author_sort Barth, Isabel
collection PubMed
description Research toward photonic biosensors for point-of-care applications and personalized medicine is driven by the need for high-sensitivity, low-cost, and reliable technology. Among the most sensitive modalities, interferometry offers particularly high performance, but typically lacks the required operational simplicity and robustness. Here, we introduce a common-path interferometric sensor based on guided-mode resonances to combine high performance with inherent stability. The sensor exploits the simultaneous excitation of two orthogonally polarized modes, and detects the relative phase change caused by biomolecular binding on the sensor surface. The wide dynamic range of the sensor, which is essential for fabrication and angle tolerance, as well as versatility, is controlled by integrating multiple, tuned structures in the field of view. This approach circumvents the trade-off between sensitivity and dynamic range, typical of other phase-sensitive modalities, without increasing complexity. Our sensor enables the challenging label-free detection of procalcitonin, a small protein (13 kDa) and biomarker for infection, at the clinically relevant concentration of 1 pg mL(−1), with a signal-to-noise ratio of 35. This result indicates the utility for an exemplary application in antibiotic guidance, and opens possibilities for detecting further clinically or environmentally relevant small molecules with an intrinsically simple and robust sensing modality.
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spelling pubmed-72649742020-06-02 Common-path interferometric label-free protein sensing with resonant dielectric nanostructures Barth, Isabel Conteduca, Donato Reardon, Christopher Johnson, Steven Krauss, Thomas F. Light Sci Appl Article Research toward photonic biosensors for point-of-care applications and personalized medicine is driven by the need for high-sensitivity, low-cost, and reliable technology. Among the most sensitive modalities, interferometry offers particularly high performance, but typically lacks the required operational simplicity and robustness. Here, we introduce a common-path interferometric sensor based on guided-mode resonances to combine high performance with inherent stability. The sensor exploits the simultaneous excitation of two orthogonally polarized modes, and detects the relative phase change caused by biomolecular binding on the sensor surface. The wide dynamic range of the sensor, which is essential for fabrication and angle tolerance, as well as versatility, is controlled by integrating multiple, tuned structures in the field of view. This approach circumvents the trade-off between sensitivity and dynamic range, typical of other phase-sensitive modalities, without increasing complexity. Our sensor enables the challenging label-free detection of procalcitonin, a small protein (13 kDa) and biomarker for infection, at the clinically relevant concentration of 1 pg mL(−1), with a signal-to-noise ratio of 35. This result indicates the utility for an exemplary application in antibiotic guidance, and opens possibilities for detecting further clinically or environmentally relevant small molecules with an intrinsically simple and robust sensing modality. Nature Publishing Group UK 2020-06-02 /pmc/articles/PMC7264974/ /pubmed/32509300 http://dx.doi.org/10.1038/s41377-020-0336-6 Text en © The Author(s) 2020 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Barth, Isabel
Conteduca, Donato
Reardon, Christopher
Johnson, Steven
Krauss, Thomas F.
Common-path interferometric label-free protein sensing with resonant dielectric nanostructures
title Common-path interferometric label-free protein sensing with resonant dielectric nanostructures
title_full Common-path interferometric label-free protein sensing with resonant dielectric nanostructures
title_fullStr Common-path interferometric label-free protein sensing with resonant dielectric nanostructures
title_full_unstemmed Common-path interferometric label-free protein sensing with resonant dielectric nanostructures
title_short Common-path interferometric label-free protein sensing with resonant dielectric nanostructures
title_sort common-path interferometric label-free protein sensing with resonant dielectric nanostructures
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7264974/
https://www.ncbi.nlm.nih.gov/pubmed/32509300
http://dx.doi.org/10.1038/s41377-020-0336-6
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