Evidence map›Paper›PMID 42143028›Full record

ArticleNature communications2026

Aberration-aware 3D localization microscopy via self-supervised neural-physics learning.

Shuang Fu, Wei Shi, Eugene A Katrukha, Xi Chen, Yue Fei, Ke Fang, Ruixiong Wang, Tianlun Zhang, Donghan Ma, Yiming Li

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Shuang FuDepartment of Biomedical Engineering, Southern University of Science and Technology, Shenzhen, China.ORCID http://orcid.org/0000-0003-0132-5707
Wei ShiDepartment of Biomedical Engineering, Southern University of Science and Technology, Shenzhen, China.ORCID http://orcid.org/0009-0009-2150-7605
Eugene A KatrukhaCell Biology, Neurobiology and Biophysics, Department of Biology, Faculty of Science, Utrecht University, Utrecht, the Netherlands.
Xi ChenSchool of Optoelectronic Engineering and Instrumentation Science, Dalian University of Technology, Dalian, China.
Yue FeiDepartment of Biomedical Engineering, Southern University of Science and Technology, Shenzhen, China.
Ke FangDepartment of Biomedical Engineering, Southern University of Science and Technology, Shenzhen, China.
Ruixiong WangDepartment of Biomedical Engineering, Southern University of Science and Technology, Shenzhen, China.
Tianlun ZhangDepartment of Biomedical Engineering, Southern University of Science and Technology, Shenzhen, China.
Donghan MaSchool of Optoelectronic Engineering and Instrumentation Science, Dalian University of Technology, Dalian, China.
Yiming LiDepartment of Biomedical Engineering, Southern University of Science and Technology, Shenzhen, China. liym2019@sustech.edu.cn.ORCID http://orcid.org/0000-0003-4109-3824

Funding

China Postdoctoral Science Foundation 2025M772887China Postdoctoral Science Foundation 2025T180788China Postdoctoral Science Foundation GZC20240651China Postdoctoral Science Foundation GZC20250546National Natural Science Foundation of China (National Science Foundation of China) 62375116
6 · The paper itself

Abstract

Single-molecule localization microscopy (SMLM) enables volumetric nanoscopy by retrieving 3D molecular positions from engineered 2D fluorescence patterns. However, achieving nanoscale resolution over large axial ranges in complex samples remains challenging due to optical aberrations and overlapping signals from high-density molecules. Here, we introduce LUNAR, a self-supervised neural-physics framework that overcomes those limitations by jointly optimizing a physical imaging model and a deep neural network. This strategy allows LUNAR to precisely infer 3D molecular positions, photon counts, and aberrations directly from raw, high-density data without prior calibration. Through simulations and experiments, we demonstrate that LUNAR achieves superior robustness and accuracy across diverse imaging conditions, consistently outperforming existing methods. We showcase its capabilities through whole-cell nanoscopy of mitochondria, nuclear pores, and neuronal cytoskeletons at large imaging depths. By uniting deep learning with physical modeling, LUNAR provides a calibration-free solution for aberration-robust 3D SMLM and establishes a general framework for adaptive, data-driven microscopy.

Indexed as

Imaging, Three-DimensionalNeural Networks, ComputerSingle Molecule ImagingAnimalsDeep LearningMicroscopy, FluorescenceMitochondriaNeurons

Identifiers

PMID42143028
PMCPMC13376372

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.