# Point spread function decoupling in computational fluorescence microscopy

**Authors:** Ziwei Wang, Wanyu Gu, Shaolei Xu, Yupei Miao, Zewei Cai, Xiang Peng, Xiaoli Liu, Liwei Liu, Qifeng Yu

PMC · DOI: 10.1038/s41377-025-02112-5 · Light, Science & Applications · 2026-01-02

## TL;DR

This paper introduces a new method for improving fluorescence microscopy by using sample priors to better characterize and enhance imaging performance.

## Contribution

The novel PSF decoupling method uses sample priors instead of sub-diffraction particles for system characterization in computational fluorescence microscopy.

## Key findings

- The PSF decoupling method enables accurate non-parametric system characterization.
- Experimental results show the method achieves imaging quality comparable to confocal microscopy.
- It supports multicolor and large depth-of-field imaging under aperture modulation.

## Abstract

Computational fluorescence microscopy constantly breaks through imaging performance through advanced optical modulation technologies; however, conventional theoretical modeling and experimental measurement approaches are challenging to meet the demand for accurate system characterization of diverse modulations. To this end, we propose a point spread function (PSF) decoupling method that is intrinsically compatible with the optimal demodulation in computational microscopic imaging modality. The critical core lies in designing a sample prior-based computational imaging strategy, in which a regular fluorescent sample instead of generally used sub-diffraction limited particles acts as a system modulator to demodulate the system response. PSF consequently can be computationally optimized through the strong support from the modulated sample prior, achieving accurate non-parametric system characterization and thereby avoiding the modeling difficulty and the low signal-to-noise ratio measurement errors of the system specificity. Experimental results across various biological tissues demonstrated and verified that the proposed PSF decoupling method enables excellent volumetric imaging comparable to confocal microscopy and multicolor, large depth-of-field imaging under aperture modulation. It provides a promising mechanism of system characterization and computational demodulation for high-contrast and high-resolution imaging of cellular and subcellular biological structures and life activities.

Sample priors enable point spread function decoupling in computational fluorescence microscopy, improving system characterization and imaging quality.

## Full-text entities

- **Genes:** ACTE1 (actin epsilon 1) [NCBI Gene 528168]
- **Diseases:** BD (MESH:D001766), CFM (MESH:C000719218)
- **Chemicals:** FITC (MESH:D016650), starch (MESH:D013213), water (MESH:D014867), TRITC (MESH:C009434), DAPI (MESH:C007293), hemicellulose (MESH:C007916), BODIPY FL (-), tetramethylrhodamine (MESH:C005358)
- **Species:** Bos taurus (bovine, species) [taxon 9913], Mus musculus (house mouse, species) [taxon 10090], Solanum tuberosum (potatoes, species) [taxon 4113], Cucurbita melopepo (species) [taxon 3665], Helianthus annuus (common sunflower, species) [taxon 4232]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12757601/full.md

## References

1 references — full list in the complete paper: https://tomesphere.com/paper/PMC12757601/full.md

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Source: https://tomesphere.com/paper/PMC12757601