Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Log inSign up
Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Blog
Job Board
Q3AS

© 2026 Aqora Quantum S.A.S.

TermsPrivacyLegal Notice

Acta Optica Sinica

Theoretical Study of Single-Pair Fluorescence Resonant Energy Transfer Spectroscopy in Microcavity

单光存 Shan Guangcun, 黄维 Huang Wei

Published Jan 1, 2009• 2 citations
Publisher
DOI
10.3788/aos20092904.1049

Related papers

Resonance fluorescence emission from single semiconductor quantum dots coupled to high-quality microcavities

Sven M. Ulrich, Ata Ulhaq, Peter Michler

Elsevier eBooks•Jan 1, 2012•0 citations

Coherent fluorescence resonance energy transfer in symmetrical clusters of fluorescent centers

Irina Basieva, Sergey K. Sekatskii, Giovanni Dietler

Chemical Physics Letters•Jan 7, 2005•2 citations

Single-molecule spectroscopy inside an optical cavity

Guangcun Shan, Shuying Bao, Wei Huang

Dynamic structural changes of macromolecules undergoing biochemical reactions can be studied using a novel single pair fluorescence resonance energy transfer (sp-FRET) tool which can be used as a nanoscale spectroscopic ruler. Although recent advances in applying such a nanoscale ruler to biological systems have been made, improvements in photon detectors and photophysical properties of the single FRET pair are still being studied. Motivated by the recent progresses in single-atom laser, we have investigated the ability to use the optical microcavity to amplify the sp-FRET signal. When the single FRET pair and the attached macromolecule of interest are placed inside an optical cavity with the emission mode of the acceptor dye in resonance with the cavity mode, quantitative modeling shows that, when adjusting the acceptor-cavity coupling parameters to be appropriate values, the acceptor fluorescence emission signal amplified by the cavity coupling mode would reach a significant value, leading to a much brighter sp-FRET spectroscopic signal. Possible applications to sp-FRET measurement of biological molecules are quantitatively examined.

Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIE•Feb 13, 2006•0 citations

Macroscopic theory of energy transfer in a microcavity

D. M. Basko

Journal of Luminescence•Sep 25, 2004•3 citations

Investigation of dye molecules in a microcavity : towards single-photon generation

Per Jönsson

•Jan 1, 2000•0 citations

Photon correlation spectroscopy of Fluorescence Resonance Energy Transfer

Andrew J. Berglund, Andrew C. Doherty, Hideo Mabuchi

We report the use of a Hanbury-Brown Twiss apparatus to measure auto- and cross-correlations from pairs of dye molecules tethered to single strands of DNA and coupled by Fluorescence Resonance Energy Transfer (FRET). We observe non-classical photon anti-bunching, and we note that certain features of the observed correlations most likely arise from conformational fluctuations in the biomolecular substrate. These techniques should provide experimental access to molecular dynamics at nanosecond (and longer) timescales.

Quantum Electronics and Laser Science Conference•May 19, 2002•0 citations
Dynamic structural changes of macromolecules undergoing biochemical reactions can be studied using a novel single pair fluorescence resonance energy transfer (sp-FRET) tool which can be used as a nanoscale spectroscopic ruler. Although recent advances in applying such a nanoscale ruler to biological systems have been made, improvements in photon detectors and photophysical properties of the single FRET pair are still being studied. Motivated by the recent progresses in single-atom laser, we have investigated the ability to use the optical microcavity to amplify the sp-FRET signal. When the single FRET pair and the attached macromolecule of interest are placed inside an optical cavity with the emission mode of the acceptor dye in resonance with the cavity mode, quantitative modeling shows that, when adjusting the acceptor-cavity coupling parameters to be appropriate values, the acceptor fluorescence emission signal amplified by the cavity coupling mode would reach a significant value, leading to a much brighter sp-FRET spectroscopic signal. Possible applications to sp-FRET measurement of biological molecules are quantitatively examined.
We report the use of a Hanbury-Brown Twiss apparatus to measure auto- and cross-correlations from pairs of dye molecules tethered to single strands of DNA and coupled by Fluorescence Resonance Energy Transfer (FRET). We observe non-classical photon anti-bunching, and we note that certain features of the observed correlations most likely arise from conformational fluctuations in the biomolecular substrate. These techniques should provide experimental access to molecular dynamics at nanosecond (and longer) timescales.