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.
Authors
- Nina Kaltenschnee
- Yunqing Li (ORCID: https://orcid.org/0009-0003-3227-2692)
- Marina S. Dietz (ORCID: https://orcid.org/0000-0003-0504-1824)
- Alexander Heckel (ORCID: https://orcid.org/0000-0003-3541-4548)
- Janik Kaufmann
- Laurell F. Kessler
- Mike Heilemann
Institutions
- Goethe University Frankfurt (DE)
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
- 0.00