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

14.7K
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...
14.7K
Three-Dimensional Microscopy in Microbiology01:28

Three-Dimensional Microscopy in Microbiology

931
Three-dimensional imaging techniques are essential in cell biology, allowing researchers to visualize intricate cellular structures with high resolution. Two prominent methods, Differential Interference Contrast Microscopy (DIC) and Confocal Scanning Laser Microscopy (CSLM), provide distinct advantages for imaging live and thick specimens, respectively.Differential Interference Contrast MicroscopyDIC microscopy enhances contrast in transparent, unstained samples by converting phase...
931

You might also read

Related Articles

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

Sort by
Same author

Nanoscale Spatial Organization of ARC High- and Low-Order Assemblies at Excitatory Synapses.

Advanced science (Weinheim, Baden-Wurttemberg, Germany)·2026
Same author

Sex-specific KDM6A-HNF4A-CREBH network controls lipoprotein cholesterol metabolism and atherosclerosis via epigenetic reprograming of hepatocytes.

Nature communications·2026
Same author

Studying Macromolecular Composition in Cell-Cell Interfaces Using 3D Membrane Reconstitution Systems.

Advanced science (Weinheim, Baden-Wurttemberg, Germany)·2026
Same author

Lipid-Facilitated Opening of the ADAM10 Sheddase Revealed by Enhanced Sampling Simulations.

Advanced science (Weinheim, Baden-Wurttemberg, Germany)·2026
Same author

Understanding excipient interactions unlocks untapped potential of RNA-lipid nanoparticles in dry powder formulations for local pulmonary delivery.

Journal of controlled release : official journal of the Controlled Release Society·2025
Same author

Allosteric control of the bacterial ClpC/ClpP protease and its hijacking by antibacterial peptides.

The EMBO journal·2025
Same journal

Topological properties of curved spacetime extended Su-Schrieffer-Heeger model.

Journal of physics. Condensed matter : an Institute of Physics journal·2026
Same journal

Influence of lattice expansion on Cr ferromagnetism in Ce<sub>(1-x)</sub>La<sub>(x)</sub>CrGe<sub>3</sub>compounds revealed by atomic-scale measurements.

Journal of physics. Condensed matter : an Institute of Physics journal·2026
Same journal

Bond-length-driven magnetic transition in quasi-one-dimensional CrSb<i>X</i><sub>3</sub>(<i>X</i>=S, Se).

Journal of physics. Condensed matter : an Institute of Physics journal·2026
Same journal

Anelasticity in MgAl2O4 spinel due to cation order-disorder.

Journal of physics. Condensed matter : an Institute of Physics journal·2026
Same journal

The influence of water on the dynamics of alternating polymers P(C<sub>8</sub>EG<sub>4</sub>) and P(C<sub>4</sub>EG<sub>4</sub>) by broadband dielectric spectroscopy.

Journal of physics. Condensed matter : an Institute of Physics journal·2026
Same journal

How surface curvature shapes water nanodroplets in air.

Journal of physics. Condensed matter : an Institute of Physics journal·2026
See all related articles

Related Experiment Video

Updated: Mar 2, 2026

Confocal and Super-Resolution Imaging of Polarized Intracellular Trafficking and Secretion of Basement Membrane Proteins During Drosophila Oogenesis
10:41

Confocal and Super-Resolution Imaging of Polarized Intracellular Trafficking and Secretion of Basement Membrane Proteins During Drosophila Oogenesis

Published on: May 19, 2022

2.6K

Super-resolution optical microscopy for studying membrane structure and dynamics.

Erdinc Sezgin1

  • 1MRC Human Immunology Unit, Weatherall Institute of Molecular Medicine, University of Oxford, OX39DS, United Kingdom.

Journal of Physics. Condensed Matter : an Institute of Physics Journal
|May 9, 2017
PubMed
Summary
This summary is machine-generated.

Super-resolution microscopy overcomes light diffraction limits to reveal nanoscale cell membrane structures. This review covers techniques and their biomembrane applications.

More Related Videos

High-resolution Spatiotemporal Analysis of Receptor Dynamics by Single-molecule Fluorescence Microscopy
15:13

High-resolution Spatiotemporal Analysis of Receptor Dynamics by Single-molecule Fluorescence Microscopy

Published on: July 25, 2014

11.9K
Tracking Single Proteins in Lipid Bilayers Using Fluorescence Microscopy
08:39

Tracking Single Proteins in Lipid Bilayers Using Fluorescence Microscopy

Published on: December 12, 2025

800

Related Experiment Videos

Last Updated: Mar 2, 2026

Confocal and Super-Resolution Imaging of Polarized Intracellular Trafficking and Secretion of Basement Membrane Proteins During Drosophila Oogenesis
10:41

Confocal and Super-Resolution Imaging of Polarized Intracellular Trafficking and Secretion of Basement Membrane Proteins During Drosophila Oogenesis

Published on: May 19, 2022

2.6K
High-resolution Spatiotemporal Analysis of Receptor Dynamics by Single-molecule Fluorescence Microscopy
15:13

High-resolution Spatiotemporal Analysis of Receptor Dynamics by Single-molecule Fluorescence Microscopy

Published on: July 25, 2014

11.9K
Tracking Single Proteins in Lipid Bilayers Using Fluorescence Microscopy
08:39

Tracking Single Proteins in Lipid Bilayers Using Fluorescence Microscopy

Published on: December 12, 2025

800

Area of Science:

  • Cell Biology
  • Biophysics
  • Microscopy

Background:

  • Cell membrane studies need high spatial and temporal resolution.
  • Conventional light microscopy is limited by light diffraction.
  • Nanoscale imaging is crucial for understanding cellular membranes.

Purpose of the Study:

  • To explain the resolution limit in light microscopy.
  • To detail the principles of super-resolution microscopy techniques.
  • To summarize applications in biomembrane research.

Main Methods:

  • Review of super-resolution microscopy principles.
  • Discussion of techniques like STED, PALM, and STORM.
  • Analysis of recent biomembrane studies using these methods.

Main Results:

  • Super-resolution microscopy achieves nanoscale resolution.
  • Various techniques offer different advantages for membrane imaging.
  • Significant advancements in understanding membrane nanostructures.

Conclusions:

  • Super-resolution microscopy is essential for nanoscale cell membrane investigation.
  • These advanced techniques provide unprecedented insights into membrane dynamics and organization.
  • Future research will continue to leverage super-resolution for cell biology discoveries.