Utilizing the predictable binding kinetics of DNA-PAINT to denoise super-resolution images

DNA-Point Accumulation for Imaging in Nanoscale Topography (DNA-PAINT) is a versatile super-resolution technique that relies on the predictable binding kinetics between fluorescent imager strands and docking strands attached to target proteins. This makes DNA-PAINT particularly suitable for multiplexing and quantitative applications, but its performance is often limited by spurious signals from non-specific binding of imager strands. Here we describe a method to remove these non-specific binding events using a statistical test to distinguish between DNA-specific and non-specific interactions. To demonstrate the method, we imaged mosaic epithelial tissues in Drosophila melanogaster egg chambers and showed that >90% of non-specific and otherwise indistinguishable signal in the super-resolved images can be removed. This denoising improves the quality of DNA-PAINT super-resolved images and is essential for accurate measurements of spatial relationships and protein quantification.

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Publication Details

Journal
Nature Communications
Published
2026-02-05
DOI
https://doi.org/10.1038/s41467-026-69304-4
Primary Topic
Advanced Fluorescence Microscopy Techniques
Type
article
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article

Utilizing the predictable binding kinetics of DNA-PAINT to denoise super-resolution images

Edward S. Allgeyer, George Sirinakis, Daniel St Johnston, Jennifer H. Richens et al.
Nature Communications
Advanced Fluorescence Microscopy Techniques
article

Utilizing the predictable binding kinetics of DNA-PAINT to denoise super-resolution images

Edward S. Allgeyer, George Sirinakis, Daniel St Johnston, Jennifer H. Richens, Ewa K. Paluch, Jeanne Lefévère-Laoide
article en

Abstract

DNA-Point Accumulation for Imaging in Nanoscale Topography (DNA-PAINT) is a versatile super-resolution technique that relies on the predictable binding kinetics between fluorescent imager strands and docking strands attached to target proteins. This makes DNA-PAINT particularly suitable for multiplexing and quantitative applications, but its performance is often limited by spurious signals from non-specific binding of imager strands. Here we describe a method to remove these non-specific binding events using a statistical test to distinguish between DNA-specific and non-specific interactions. To demonstrate the method, we imaged mosaic epithelial tissues in Drosophila melanogaster egg chambers and showed that >90% of non-specific and otherwise indistinguishable signal in the super-resolved images can be removed. This denoising improves the quality of DNA-PAINT super-resolved images and is essential for accurate measurements of spatial relationships and protein quantification.

Nature CommunicationsVol. 17(1)
University of Cambridge (GB), The Gurdon Institute (GB)
Openalex Percentile: Top 69%
Advanced Fluorescence Microscopy Techniques
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