Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Super-resolution Fluorescence Microscopy01:37

Super-resolution Fluorescence Microscopy

7.8K
Super-resolution fluorescence microscopy (SRFM) provides a better resolution than conventional fluorescence microscopy by reducing the point spread function (PSF). PSF is the light intensity distribution from a point that causes it to appear blurred. Due to PSF, each fluorescing point appears bigger than its actual size, and it is the PSF interference of nearby fluorophores that causes the blurred image. Various approaches to achieving higher resolution through SRFM have recently been...
7.8K
Protein Dynamics in Living Cells01:19

Protein Dynamics in Living Cells

2.3K
Different fluorescence-based techniques are used to study the protein dynamics in living cells. These techniques include FRAP, FRET, and PET.
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...
2.3K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Multifocal Pixel/Photon-Reassignment FLIM (MPPR-FLIM): A Super-Resolution Analytical Tool for Characterizing Subcellular Fluorescence Lifetime Heterogeneity via TCSPC.

Analytical chemistry·2026
Same author

Deep-learning-assisted scattering structured-illumination confocal microscopy for industrial super-resolution imaging.

Optics express·2026
Same author

In Vivo Hyperspectral CARS Imaging Reveals Photobiomodulation-Driven Remodeling of Fatty Acid Homeostasis in an AD Mouse Model.

Analytical chemistry·2026
Same author

Ice-phase optothermal tweezers.

Nature communications·2026
Same author

Investigation of Drug Responses in 3D Tumor Spheroid Models Using Two-Photon Scanning Structured Illumination Super-Resolution Microscopy with Frequency-Specific Denoising Enhancement.

IEEE transactions on medical imaging·2026
Same author

Rapid Generation of Subject-Specific Human Models With Detailed Tissue Structures for Timely Individualized SAR Assessment.

Magnetic resonance in medicine·2026
Same journal

Heterojunction Gate-Empowered OPECT Aptasensing: A Valid Protocol for Realizing High Current Gain at Low Electron Donor Dependency.

Analytical chemistry·2026
Same journal

Development of a Tapping-Mode Scanning Probe Electrospray Ionization Platform for High-Sensitivity and Long-Term Stability in Single-Cell Mass Spectrometry Imaging of Tissue.

Analytical chemistry·2026
Same journal

A Solid-State Near-Infrared Fluorescent Probe by a Synergistic Extended Conjugated System for Detecting Cys with Long-Term Imaging in Orthotopic Bladder Cancer.

Analytical chemistry·2026
Same journal

Air-Based Porous Array Dielectric Barrier Discharge Ionization Source for Explosive Trace Detection.

Analytical chemistry·2026
Same journal

PSAQ<sup>+1</sup>: Absolute Protein Quantification Using a <sup>13</sup>C<sub>1</sub>-Labeled Protein Standard, Coisolation of Peptide Pairs and LC-PRM.

Analytical chemistry·2026
Same journal

Heterojunction-Enhanced Interfacial Evanescent-Tunable Fiber Optic Probe for Amplification-free CRISPR/Cas12a-Based Rapid and Ultrasensitive Detection of MPXV.

Analytical chemistry·2026
See all related articles

Related Experiment Video

Updated: Sep 16, 2025

Fluorescence Lifetime Imaging of Molecular Rotors in Living Cells
09:45

Fluorescence Lifetime Imaging of Molecular Rotors in Living Cells

Published on: February 9, 2012

25.4K

Rapid Fluorescence Lifetime Imaging through One-Dimensional Deep Learning Optimization.

Xinwei Gao1, Yanfeng Liu1, Yong Guo1

  • 1State Key Laboratory of Radio Frequency Heterogeneous Integration (Shenzhen University); College of Physics and Optoelectronic Engineering, Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province Shenzhen University, Shenzhen 518060, P. R. China.

Analytical Chemistry
|July 11, 2025
PubMed
Summary
This summary is machine-generated.

A new deep learning method using 1D channel attention convolutional neural networks (1D CANNs) significantly speeds up fluorescence lifetime imaging (FLIM) analysis. This efficient approach reduces computational load and enhances accuracy for biomedical applications.

More Related Videos

Visualizing Protein Kinase A Activity In Head-fixed Behaving Mice Using In Vivo Two-photon Fluorescence Lifetime Imaging Microscopy
10:41

Visualizing Protein Kinase A Activity In Head-fixed Behaving Mice Using In Vivo Two-photon Fluorescence Lifetime Imaging Microscopy

Published on: June 7, 2019

8.6K
Fluorescence Lifetime Macro Imager for Biomedical Applications
06:01

Fluorescence Lifetime Macro Imager for Biomedical Applications

Published on: April 7, 2023

818

Related Experiment Videos

Last Updated: Sep 16, 2025

Fluorescence Lifetime Imaging of Molecular Rotors in Living Cells
09:45

Fluorescence Lifetime Imaging of Molecular Rotors in Living Cells

Published on: February 9, 2012

25.4K
Visualizing Protein Kinase A Activity In Head-fixed Behaving Mice Using In Vivo Two-photon Fluorescence Lifetime Imaging Microscopy
10:41

Visualizing Protein Kinase A Activity In Head-fixed Behaving Mice Using In Vivo Two-photon Fluorescence Lifetime Imaging Microscopy

Published on: June 7, 2019

8.6K
Fluorescence Lifetime Macro Imager for Biomedical Applications
06:01

Fluorescence Lifetime Macro Imager for Biomedical Applications

Published on: April 7, 2023

818

Area of Science:

  • Biomedical optics
  • Computational biology
  • Deep learning applications

Background:

  • Traditional fluorescence lifetime imaging (FLIM) analysis is computationally intensive.
  • Existing methods often require complex data-fitting techniques.
  • There is a need for faster and more efficient FLIM data processing.

Purpose of the Study:

  • To develop a hardware-efficient deep learning approach for rapid FLIM data analysis.
  • To improve the speed and reduce computational requirements of FLIM.
  • To validate the performance of 1D CANNs on FLIM and related imaging techniques.

Main Methods:

  • Utilized one-dimensional channel attention convolutional neural networks (1D CANNs).
  • Trained 1D CANNs on raw time-correlated single-photon counting (TCSPC) data.
  • Applied 1D CANNs to fluorescence lifetime fitting, phosphorescence lifetime imaging (PLIM), and STED-FLIM.

Main Results:

  • Achieved high efficiency and speed in FLIM data processing with 1D CANNs.
  • Demonstrated strong consistency between predicted and ground truth lifetime maps.
  • Obtained prediction errors within 10% for PLIM and improved spatial resolution in STED-FLIM.

Conclusions:

  • 1D CANNs offer a computationally efficient and accurate alternative for FLIM analysis.
  • The method shows broad potential in various biomedical and photonics applications, including disease diagnosis and advanced imaging.
  • 1D CANNs are robust across different photon count conditions.