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

Author

Listed:
  • Yaping Wang

    (Beijing University of Technology)

  • Marion C. Lang

    (Beijing University of Technology
    Carl Zeiss Microscopy GmbH ZEISS Group)

  • Jinsong Lu

    (Beijing University of Technology)

  • Mingqian Suo

    (Beijing University of Technology)

  • Mengcong Du

    (Beijing University of Technology)

  • Yubin Hou

    (Beijing University of Technology
    Ministry of Education
    Beijing Engineering Research Center of Laser Technology
    Beijing Colleges and Universities Engineering Research Center of Advanced Laser Manufacturing)

  • Xiu-Hong Wang

    (Beijing University of Technology
    Ministry of Education
    Beijing Engineering Research Center of Laser Technology
    Beijing Colleges and Universities Engineering Research Center of Advanced Laser Manufacturing)

  • Pu Wang

    (Beijing University of Technology
    Ministry of Education
    Beijing Engineering Research Center of Laser Technology
    Beijing Colleges and Universities Engineering Research Center of Advanced Laser Manufacturing)

Abstract

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.

Suggested Citation

  • Yaping Wang & Marion C. Lang & Jinsong Lu & Mingqian Suo & Mengcong Du & Yubin Hou & Xiu-Hong Wang & Pu Wang, 2022. "Demonstration of intracellular real-time molecular quantification via FRET-enhanced optical microcavity," Nature Communications, Nature, vol. 13(1), pages 1-10, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-34547-4
    DOI: 10.1038/s41467-022-34547-4
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    References listed on IDEAS

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    1. Bumki Min & Eric Ostby & Volker Sorger & Erick Ulin-Avila & Lan Yang & Xiang Zhang & Kerry Vahala, 2009. "High-Q surface-plasmon-polariton whispering-gallery microcavity," Nature, Nature, vol. 457(7228), pages 455-458, January.
    2. Weijian Chen & Şahin Kaya Özdemir & Guangming Zhao & Jan Wiersig & Lan Yang, 2017. "Exceptional points enhance sensing in an optical microcavity," Nature, Nature, vol. 548(7666), pages 192-196, August.
    3. Alasdair H. Fikouras & Marcel Schubert & Markus Karl & Jothi D. Kumar & Simon J. Powis & Andrea Di Falco & Malte C. Gather, 2018. "Non-obstructive intracellular nanolasers," Nature Communications, Nature, vol. 9(1), pages 1-7, December.
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