Wash‐Free Multi‐Target Super‐Resolution Microscopy With Photocaged DNA Labels

Super-resolution microscopy with DNA-fluorophore labels is primed for multi-target imaging of cell biological samples. However, direct interaction with the sample is required to exchange or add DNA-fluorophore labels in each imaging round, which can impair the accuracy of the imaging data at the nanometer scale. To bypass this requirement, we introduce PhotoPAINT, a wash-free method that employs DNA oligonucleotides equipped with photocaging groups. Irradiation with light removes these photo-modulatable groups and changes the hybridization properties of DNA labels, enabling light-modulated targeting. We demonstrate this concept by imaging various cellular targets with confocal microscopy, single-molecule localization microscopy (SMLM), and stimulated emission depletion (STED) microscopy.

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Publication Details

Journal
Angewandte Chemie International Edition
Published
2026-03-13
DOI
https://doi.org/10.1002/anie.202526137
Primary Topic
Advanced Fluorescence Microscopy Techniques
Type
article
Field-Weighted Citation Impact
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article

Wash‐Free Multi‐Target Super‐Resolution Microscopy With Photocaged DNA Labels

Nina Kaltenschnee, Yunqing Li, Marina S. Dietz, Alexander Heckel et al.
Angewandte Chemie International Edition
Advanced Fluorescence Microscopy Techniques
article

Wash‐Free Multi‐Target Super‐Resolution Microscopy With Photocaged DNA Labels

Nina Kaltenschnee, Yunqing Li, Marina S. Dietz, Alexander Heckel, Janik Kaufmann, Laurell F. Kessler, Mike Heilemann
article en

Abstract

Super-resolution microscopy with DNA-fluorophore labels is primed for multi-target imaging of cell biological samples. However, direct interaction with the sample is required to exchange or add DNA-fluorophore labels in each imaging round, which can impair the accuracy of the imaging data at the nanometer scale. To bypass this requirement, we introduce PhotoPAINT, a wash-free method that employs DNA oligonucleotides equipped with photocaging groups. Irradiation with light removes these photo-modulatable groups and changes the hybridization properties of DNA labels, enabling light-modulated targeting. We demonstrate this concept by imaging various cellular targets with confocal microscopy, single-molecule localization microscopy (SMLM), and stimulated emission depletion (STED) microscopy.

Angewandte Chemie International Edition
Goethe University Frankfurt (DE)
Openalex Percentile: Top 21%
Advanced Fluorescence Microscopy Techniques
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