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

10.5K
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...
10.5K
Protein Dynamics in Living Cells01:19

Protein Dynamics in Living Cells

2.4K
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...
2.4K

You might also read

Related Articles

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

Sort by
Same author

Neural timescales from a computational perspective.

Nature neuroscience·2026
Same author

Coupling of cargo to the autophagy receptor is a critical step in ER-phagy.

Science advances·2026
Same author

Chromatix: a differentiable, GPU-accelerated wave-optics library.

Nature methods·2026
Same author

Nuclear SUN2 coordinates endothelial cell-matrix interactions to regulate blood vessel homeostasis and barrier function.

bioRxiv : the preprint server for biology·2026
Same author

A multimodal adaptive optical microscope for in vivo imaging from molecules to organisms.

Nature methods·2026
Same author

Mesoglea biogenesis reveals a cryptic aboral valve for pressure regulation in cnidarian morphogenesis.

Science advances·2026

Related Experiment Video

Updated: Oct 21, 2025

Single-Molecule Tracking Microscopy - A Tool for Determining the Diffusive States of Cytosolic Molecules
10:20

Single-Molecule Tracking Microscopy - A Tool for Determining the Diffusive States of Cytosolic Molecules

Published on: September 5, 2019

8.4K

Deep learning enables fast and dense single-molecule localization with high accuracy.

Artur Speiser1,2,3,4, Lucas-Raphael Müller5,6, Philipp Hoess5

  • 1Machine Learning in Science, Excellence Cluster Machine Learning, Tübingen University, Tübingen, Germany.

Nature Methods
|September 4, 2021
PubMed
Summary
This summary is machine-generated.

Deep learning tool DECODE enhances single-molecule localization microscopy (SMLM) by enabling high-density 3D emitter localization. This breakthrough overcomes limitations in imaging speed and labeling density for advanced cellular imaging.

More Related Videos

Multi-color Localization Microscopy of Single Membrane Proteins in Organelles of Live Mammalian Cells
11:06

Multi-color Localization Microscopy of Single Membrane Proteins in Organelles of Live Mammalian Cells

Published on: June 30, 2018

8.7K
Simultaneous Multicolor Imaging of Biological Structures with Fluorescence Photoactivation Localization Microscopy
12:51

Simultaneous Multicolor Imaging of Biological Structures with Fluorescence Photoactivation Localization Microscopy

Published on: December 9, 2013

9.1K

Related Experiment Videos

Last Updated: Oct 21, 2025

Single-Molecule Tracking Microscopy - A Tool for Determining the Diffusive States of Cytosolic Molecules
10:20

Single-Molecule Tracking Microscopy - A Tool for Determining the Diffusive States of Cytosolic Molecules

Published on: September 5, 2019

8.4K
Multi-color Localization Microscopy of Single Membrane Proteins in Organelles of Live Mammalian Cells
11:06

Multi-color Localization Microscopy of Single Membrane Proteins in Organelles of Live Mammalian Cells

Published on: June 30, 2018

8.7K
Simultaneous Multicolor Imaging of Biological Structures with Fluorescence Photoactivation Localization Microscopy
12:51

Simultaneous Multicolor Imaging of Biological Structures with Fluorescence Photoactivation Localization Microscopy

Published on: December 9, 2013

9.1K

Area of Science:

  • Biophysics
  • Microscopy
  • Computational Biology

Background:

  • Single-molecule localization microscopy (SMLM) achieves nanometer resolution for cellular imaging.
  • Standard SMLM analysis requires sparse emitters, limiting imaging speed and labeling density.

Purpose of the Study:

  • To develop a deep learning-based computational tool for high-density, accurate single-emitter localization in 3D SMLM.
  • To overcome the limitations of conventional SMLM analysis algorithms.

Main Methods:

  • Development of DECODE (deep context dependent), a novel deep learning algorithm for SMLM data analysis.
  • Benchmarking DECODE against existing SMLM localization algorithms using diverse datasets.

Main Results:

  • DECODE demonstrated superior performance in detection accuracy and localization error across 12 benchmark datasets.
  • The tool enables high-density 3D emitter localization with high accuracy for various imaging conditions.
  • DECODE facilitated fast, dynamic live-cell SMLM imaging with reduced light exposure and ultra-high labeling density.

Conclusions:

  • DECODE significantly advances SMLM analysis by enabling high-density emitter localization.
  • The software provides a user-friendly solution to reduce imaging times and increase localization density in SMLM.
  • This tool will broadly benefit researchers in cellular imaging and biophysics.