Quantitative Stimulated Emission Depletion (STED) Microscopy with DNA-Fluorophore Labels
Stimulated emission depletion (STED) microscopy enables super-resolution imaging of complex biological samples in 3D, in large volumes, and live. However, molecular quantification with STED has remained underexplored. Here, we present a straightforward approach for quantitative STED that enables molecule counting. For this purpose, we designed DNA-fluorophore labels that enable signal amplification and allow for reliable intensity-based quantitative imaging. We demonstrate accurate molecule counting on DNA origami. Furthermore, we visualized and quantified EGF receptor monomers and dimers in cells. In summary, we introduce a robust, fast, and easy-to-implement tool for quantitative STED microscopy with single-protein resolution.
Authors
- Yunqing Li (ORCID: https://orcid.org/0009-0003-3227-2692)
- Ashwin Balakrishnan (ORCID: https://orcid.org/0000-0003-4059-8345)
- Laurell F. Kessler
- Mike Heilemann
Institutions
- Goethe University Frankfurt (DE)
Publication Details
- Journal
- ACS Nano
- Published
- 2026-02-03
- DOI
- https://doi.org/10.1021/acsnano.5c21411
- Primary Topic
- Advanced Fluorescence Microscopy Techniques
- Type
- article
- Field-Weighted Citation Impact
- 0.00