One step 4× and 12× 3D-ExM enables robust super-resolution microscopy of nanoscale cellular structures

Super-resolution microscopy has become an indispensable tool across diverse research fields, offering unprecedented insights into biological architectures with nanometer scale resolution. Compared with traditional nanometer-scale imaging methods such as electron microscopy, super-resolution microscopy offers several advantages, including the simultaneous labeling of multiple target biomolecules with high specificity and simpler sample preparation, making it accessible to most researchers. In this study, we introduce two optimized methods of super-resolution imaging: 4-fold and 12-fold 3D-isotropic and preserved Expansion Microscopy (4× and 12× 3D-ExM). 3D-ExM is a straightforward expansion microscopy technique featuring a single-step process, providing robust and reproducible 3D isotropic expansion for both 2D and 3D cell culture models. With standard confocal microscopy, 12× 3D-ExM achieves a lateral resolution of <30 nm, enabling the visualization of nanoscale structures, including chromosomes, kinetochores, nuclear pore complexes, and Epstein-Barr virus particles. These results demonstrate that 3D-ExM provides cost-effective and user-friendly super-resolution microscopy, making it highly suitable for a wide range of cell biology research, including studies on cellular and chromatin architectures.

Authors

Institutions

Publication Details

Journal
The Journal of Cell Biology
Published
2024-12-03
DOI
https://doi.org/10.1083/jcb.202407116
Citations
9
Primary Topic
Advanced Fluorescence Microscopy Techniques
Type
article
Field-Weighted Citation Impact
5.96

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

One step 4× and 12× 3D-ExM enables robust super-resolution microscopy of nanoscale cellular structures

Motoki Takaku, Roshan X. Norman, Nathan M. Sherer, Quincy Rosemarie et al.
9 citations
The Journal of Cell Biology
Advanced Fluorescence Microscopy Techniques
5.96
article

One step 4× and 12× 3D-ExM enables robust super-resolution microscopy of nanoscale cellular structures

Motoki Takaku, Roshan X. Norman, Nathan M. Sherer, Quincy Rosemarie, Jonathan Loi, Mark E. Burkard, Sydney L. Lesko, Emma E. Recchia, Aussie Suzuki, Yu-Chia Chen, Smit Patel
article en
9 citations

Abstract

Super-resolution microscopy has become an indispensable tool across diverse research fields, offering unprecedented insights into biological architectures with nanometer scale resolution. Compared with traditional nanometer-scale imaging methods such as electron microscopy, super-resolution microscopy offers several advantages, including the simultaneous labeling of multiple target biomolecules with high specificity and simpler sample preparation, making it accessible to most researchers. In this study, we introduce two optimized methods of super-resolution imaging: 4-fold and 12-fold 3D-isotropic and preserved Expansion Microscopy (4× and 12× 3D-ExM). 3D-ExM is a straightforward expansion microscopy technique featuring a single-step process, providing robust and reproducible 3D isotropic expansion for both 2D and 3D cell culture models. With standard confocal microscopy, 12× 3D-ExM achieves a lateral resolution of <30 nm, enabling the visualization of nanoscale structures, including chromosomes, kinetochores, nuclear pore complexes, and Epstein-Barr virus particles. These results demonstrate that 3D-ExM provides cost-effective and user-friendly super-resolution microscopy, making it highly suitable for a wide range of cell biology research, including studies on cellular and chromatin architectures.

The Journal of Cell BiologyVol. 224(2)
University of Wisconsin–Madison (US), University of North Dakota (US), University of Wisconsin Carbone Cancer Center (US)
Wisconsin Alumni Research Foundation, University of Wisconsin-Madison, University of Wisconsin Carbone Cancer Center, National Institutes of Health
Industry, innovation and infrastructure
Openalex Percentile: Top 4%
Advanced Fluorescence Microscopy Techniques
5.96
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.