Related Experiment Video
Updated: Jan 10, 2026

Dual-Color Fluorescence Cross-Correlation Spectroscopy to Study Protein-Protein Interaction and Protein Dynamics in Live Cells
Published on: December 11, 2021
Phasor theory of fluorescence lifetime imaging utilized on a maximum range of frequencies for prostate tissue
Ryan A L Schoop1,2, Lotte M de Roode1,2, Alba Alfonso-García3
1Image-Guided Surgery, Department of Surgery, Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX Amsterdam, The Netherlands.
Abstract:
Fluorescence lifetime imaging (FLIm) can detect macroscopic tumor tissue in various organs by measuring tissue autofluorescence, making it a compelling tool for surgical guidance. However, the fluorescence lifetime characteristics of tissue autofluorescence are complex due to the unpredictable microenvironment of the biomolecules in tissue, which complicates data interpretation. Nevertheless, the phasor analysis method is computationally fast and easily interpretable, making it appealing for clinical applications of FLIm. While many implementations of the phasor analysis operate only at a single frequency or a few harmonic frequencies, the phasor theory applied to pulse sampling FLIm as presented in this study leverages the maximum amount of frequency information, thereby extending the set of features available for tissue characterization. The clinical effectiveness of utilizing the maximum range of frequencies in phasor theory applied to pulse-sampling FLIm is demonstrated by investigating tumor detection in ex vivo tissue from 12 patients with prostate cancer. By accounting for the zonal anatomy of the prostate, it is shown that the degree of separability between healthy and tumor tissue is a function of frequency, and hence, the ability to access arbitrary frequency content can improve tumor detection in clinical guidance.
More Related Videos
10:41Visualizing Protein Kinase A Activity In Head-fixed Behaving Mice Using In Vivo Two-photon Fluorescence Lifetime Imaging Microscopy
Published on: June 7, 2019
10:23Time-Resolved Fluorescence Anisotropy from Single Molecules for Characterizing Local Flexibility in Biomolecules
Published on: April 25, 2025
Related Concept Videos
Super-resolution Fluorescence Microscopy
Protein Dynamics in Living Cells
Fluorescent recovery after photobleaching (FRAP) is a fluorescent-protein-based detection technique used to quantify protein movement rates within the cell. This method exposes a small portion of the cell to an intense laser beam. The laser beam causes permanent photobleaching of the fluorophore-tagged proteins in the exposed region. As the bleached...