Evidence map›Paper›PMID 39625433›Full record

ArticleThe Journal of cell biology2025

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

Roshan X Norman, Yu-Chia Chen, Emma E Recchia, Jonathan Loi, Quincy Rosemarie, Sydney L Lesko, Smit Patel, Nathan Sherer, Motoki Takaku, Mark E Burkard and 1 more

Abstract read
In one paragraph

Article in The Journal of cell biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Roshan X Norman *Biophysics Graduate Program, University of Wisconsin-Madison , Madison, WI, USA.ORCID 0000-0002-2444-519X
Yu-Chia Chen *Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison, Madison, WI, USA.ORCID 0000-0002-2404-7597
Emma E Recchia *Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison, Madison, WI, USA.ORCID 0000-0002-6948-0220
Jonathan Loi *Biophysics Graduate Program, University of Wisconsin-Madison , Madison, WI, USA.ORCID 0000-0001-5229-2293
Quincy RosemarieDepartment of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison, Madison, WI, USA.ORCID 0000-0002-0394-1573
Sydney L LeskoDepartment of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison, Madison, WI, USA.ORCID 0000-0002-2344-8575
Smit PatelDepartment of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison, Madison, WI, USA.ORCID 0009-0007-4753-6282
Nathan ShererDepartment of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison, Madison, WI, USA.ORCID 0000-0001-9974-236X
Motoki TakakuDepartment of Biomedical Science, University of North Dakota School of Medicine and Health Science, Grand Forks, ND, USA.ORCID 0000-0002-8652-2541
Mark E BurkardBiophysics Graduate Program, University of Wisconsin-Madison , Madison, WI, USA.ORCID 0000-0002-4215-7722
Aussie SuzukiBiophysics Graduate Program, University of Wisconsin-Madison , Madison, WI, USA.ORCID 0000-0001-7390-5116

Funding

UW COMPREHENSIVE CANCER CENTER SUPPORTP30CA014520 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Justine Yang Bruce · 1985 to 2026
$142.6M
Visualizing EBV and HCMV DNA Dynamics During InfectionP01CA022443 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Paul F. Lambert · 1985 to 2026
$53.1M
Center for Structural Biology of HIV RNAU54AI170660 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ALICE TELESNITSKY · 2022 to 2026
$32.1M
The Cell Biology of HIV-1 Genome TraffickingR01AI110221 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI Nathan M Sherer · 2014 to 2026
$4.4M
Impact of chromosomal instability on sensitivity to microtubule-targeting drugs in breast cancerR01CA234904 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI BURKARD, MARK E, WEAVER, BETH A · 2019 to 2023
$2.7M
Chromosome dynamics and organizations necessary for faithful chromosome segregationR35GM147525 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI Aussie Suzuki · 2022 to 2026
$2.5M
Role of nucleosome architecture in cellular reprogrammingR01GM148729 · NIGMS · UNIVERSITY OF NORTH DAKOTA · PI Motoki Takaku · 2023 to 2026
$1.4M
Mechanisms of Plk1 at the mitotic centromereR01GM141068 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI WEAVER, BETH A · 2021 to 2024
$1.2M
The Cell Biology of HIV-1 Genome TraffickingR56AI110221 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI SHERER, NATHAN M · 2024 to 2024
$457k
McArdle Laboratory for Cancer ResearchNCI NIH HHS P01 CA022443NCI NIH HHS P30 CA014520NCI NIH HHS R01 CA234904NIAID NIH HHS R01 AI110221NIAID NIH HHS R56 AI110221NIAID NIH HHS U54 AI170660NIGMS NIH HHS R01 GM141068NIGMS NIH HHS R01 GM148729NIGMS NIH HHS R35 GM147525NIH HHS R35GM147525University of Wisconsin Carbone Cancer CenterUniversity of Wisconsin-MadisonWisconsin Alumni Research Foundation
6 · The paper itself

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.

Indexed as

Imaging, Three-DimensionalChromosomesHeLa CellsHerpesvirus 4, HumanHumansKinetochoresMicroscopy, ConfocalMicroscopy, FluorescenceNuclear Pore

Identifiers

PMID39625433
PMCPMC11613959

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.