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On-the-fly decoding luminescence lifetimes in the microsecond region for lanthanide-encoded suspension arrays

Author

Listed:
  • Yiqing Lu

    (Advanced Cytometry Laboratories, ARC Centre of Excellence for Nanoscale BioPhotonics (CNBP), Macquarie University)

  • Jie Lu

    (Advanced Cytometry Laboratories, ARC Centre of Excellence for Nanoscale BioPhotonics (CNBP), Macquarie University)

  • Jiangbo Zhao

    (Advanced Cytometry Laboratories, ARC Centre of Excellence for Nanoscale BioPhotonics (CNBP), Macquarie University)

  • Janet Cusido

    (Laboratory for Molecular Photonics, University of Miami, 1301 Memorial Drive)

  • Françisco M Raymo

    (Laboratory for Molecular Photonics, University of Miami, 1301 Memorial Drive)

  • Jingli Yuan

    (State Key Laboratory of Fine Chemicals, School of Chemistry, Dalian University of Technology)

  • Sean Yang

    (Newport Instruments, 3345 Hopi Place)

  • Robert C. Leif

    (Newport Instruments, 3345 Hopi Place)

  • Yujing Huo

    (Tsinghua University)

  • James A. Piper

    (Advanced Cytometry Laboratories, ARC Centre of Excellence for Nanoscale BioPhotonics (CNBP), Macquarie University)

  • J Paul Robinson

    (Purdue University Cytometry Laboratories, Bindley Bioscience Center, Purdue University)

  • Ewa M. Goldys

    (Advanced Cytometry Laboratories, ARC Centre of Excellence for Nanoscale BioPhotonics (CNBP), Macquarie University)

  • Dayong Jin

    (Advanced Cytometry Laboratories, ARC Centre of Excellence for Nanoscale BioPhotonics (CNBP), Macquarie University
    Purdue University Cytometry Laboratories, Bindley Bioscience Center, Purdue University)

Abstract

Significant multiplexing capacity of optical time-domain coding has been recently demonstrated by tuning luminescence lifetimes of the upconversion nanoparticles called ‘τ-Dots’. It provides a large dynamic range of lifetimes from microseconds to milliseconds, which allows creating large libraries of nanotags/microcarriers. However, a robust approach is required to rapidly and accurately measure the luminescence lifetimes from the relatively slow-decaying signals. Here we show a fast algorithm suitable for the microsecond region with precision closely approaching the theoretical limit and compatible with the rapid scanning cytometry technique. We exploit this approach to further extend optical time-domain multiplexing to the downconversion luminescence, using luminescence microspheres wherein lifetimes are tuned through luminescence resonance energy transfer. We demonstrate real-time discrimination of these microspheres in the rapid scanning cytometry, and apply them to the multiplexed probing of pathogen DNA strands. Our results indicate that tunable luminescence lifetimes have considerable potential in high-throughput analytical sciences.

Suggested Citation

  • Yiqing Lu & Jie Lu & Jiangbo Zhao & Janet Cusido & Françisco M Raymo & Jingli Yuan & Sean Yang & Robert C. Leif & Yujing Huo & James A. Piper & J Paul Robinson & Ewa M. Goldys & Dayong Jin, 2014. "On-the-fly decoding luminescence lifetimes in the microsecond region for lanthanide-encoded suspension arrays," Nature Communications, Nature, vol. 5(1), pages 1-8, September.
  • Handle: RePEc:nat:natcom:v:5:y:2014:i:1:d:10.1038_ncomms4741
    DOI: 10.1038/ncomms4741
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