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Demonstration of intracellular real-time molecular quantification via FRET-enhanced optical microcavity

Single cell analysis is crucial for elucidating cellular diversity and heterogeneity as well as for medical diagnostics operating at the ultimate detection limit. Although superbly sensitive biosensors have been developed using the strongly enhanced evanescent fields provided by optical microcavitie...

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Autores principales: Wang, Yaping, Lang, Marion C., Lu, Jinsong, Suo, Mingqian, Du, Mengcong, Hou, Yubin, Wang, Xiu-Hong, Wang, Pu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9637138/
https://www.ncbi.nlm.nih.gov/pubmed/36335126
http://dx.doi.org/10.1038/s41467-022-34547-4
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author Wang, Yaping
Lang, Marion C.
Lu, Jinsong
Suo, Mingqian
Du, Mengcong
Hou, Yubin
Wang, Xiu-Hong
Wang, Pu
author_facet Wang, Yaping
Lang, Marion C.
Lu, Jinsong
Suo, Mingqian
Du, Mengcong
Hou, Yubin
Wang, Xiu-Hong
Wang, Pu
author_sort Wang, Yaping
collection PubMed
description Single cell analysis is crucial for elucidating cellular diversity and heterogeneity as well as for medical diagnostics operating at the ultimate detection limit. Although superbly sensitive biosensors have been developed using the strongly enhanced evanescent fields provided by optical microcavities, real-time quantification of intracellular molecules remains challenging due to the extreme low quantity and limitations of the current techniques. Here, we introduce an active-mode optical microcavity sensing stage with enhanced sensitivity that operates via Förster resonant energy transferring (FRET) mechanism. The mutual effects of optical microcavity and FRET greatly enhances the sensing performance by four orders of magnitude compared to pure Whispering gallery mode (WGM) microcavity sensing system. We demonstrate distinct sensing mechanism of FRET-WGM from pure WGM. Predicted lasing wavelengths of both donor and acceptor by theoretical calculations are in perfect agreement with the experimental data. The proposed sensor enables quantitative molecular analysis at single cell resolution, and real-time monitoring of intracellular molecules over extended periods while maintaining the cell viability. By achieving high sensitivity at single cell level, our approach provides a path toward FRET-enhanced real-time quantitative analysis of intracellular molecules.
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spelling pubmed-96371382022-11-07 Demonstration of intracellular real-time molecular quantification via FRET-enhanced optical microcavity Wang, Yaping Lang, Marion C. Lu, Jinsong Suo, Mingqian Du, Mengcong Hou, Yubin Wang, Xiu-Hong Wang, Pu Nat Commun Article Single cell analysis is crucial for elucidating cellular diversity and heterogeneity as well as for medical diagnostics operating at the ultimate detection limit. Although superbly sensitive biosensors have been developed using the strongly enhanced evanescent fields provided by optical microcavities, real-time quantification of intracellular molecules remains challenging due to the extreme low quantity and limitations of the current techniques. Here, we introduce an active-mode optical microcavity sensing stage with enhanced sensitivity that operates via Förster resonant energy transferring (FRET) mechanism. The mutual effects of optical microcavity and FRET greatly enhances the sensing performance by four orders of magnitude compared to pure Whispering gallery mode (WGM) microcavity sensing system. We demonstrate distinct sensing mechanism of FRET-WGM from pure WGM. Predicted lasing wavelengths of both donor and acceptor by theoretical calculations are in perfect agreement with the experimental data. The proposed sensor enables quantitative molecular analysis at single cell resolution, and real-time monitoring of intracellular molecules over extended periods while maintaining the cell viability. By achieving high sensitivity at single cell level, our approach provides a path toward FRET-enhanced real-time quantitative analysis of intracellular molecules. Nature Publishing Group UK 2022-11-05 /pmc/articles/PMC9637138/ /pubmed/36335126 http://dx.doi.org/10.1038/s41467-022-34547-4 Text en © The Author(s) 2022 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 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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Wang, Yaping
Lang, Marion C.
Lu, Jinsong
Suo, Mingqian
Du, Mengcong
Hou, Yubin
Wang, Xiu-Hong
Wang, Pu
Demonstration of intracellular real-time molecular quantification via FRET-enhanced optical microcavity
title Demonstration of intracellular real-time molecular quantification via FRET-enhanced optical microcavity
title_full Demonstration of intracellular real-time molecular quantification via FRET-enhanced optical microcavity
title_fullStr Demonstration of intracellular real-time molecular quantification via FRET-enhanced optical microcavity
title_full_unstemmed Demonstration of intracellular real-time molecular quantification via FRET-enhanced optical microcavity
title_short Demonstration of intracellular real-time molecular quantification via FRET-enhanced optical microcavity
title_sort demonstration of intracellular real-time molecular quantification via fret-enhanced optical microcavity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9637138/
https://www.ncbi.nlm.nih.gov/pubmed/36335126
http://dx.doi.org/10.1038/s41467-022-34547-4
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