A Near-Infrared Aptamer:Dye System For Live-Cell Super-Resolution RNA Imaging
Despite their advantageous properties for live-cell imaging and super-resolution microscopy, high-performance silicon rhodamine (SiR) near-infrared (NIR) probes are still rarely employed in RNA imaging via fluorescent light-up aptamers (FLAPs). Here, we developed the SiRiuS:SiR-5 system through a combined evolutionary approach: evolving the aptamer via fluorescence-activated cell sorting (FACS), along with targeted mutations, truncations, and rational design, and improvement of the dye by systematic chemical derivatization. This resulted in an aptamer:dye pair with high fluorogenicity and photostability, specifically optimized for visualization of RNAs in mammalian live cells. Our system demonstrates strong fluorescence enhancement in live-cell imaging, enabling time-resolved imaging of dynamic processes such as stress-granule formation. Notably, we validate its application in STED super-resolution microscopy, establishing it as a powerful NIR imaging platform for RNA structures below the diffraction limit. Its orthogonality to existing FLAPs operating in the yellow-orange spectrum further broadens its versatility for exploring complex RNA dynamics in live cells.
Authors
- Erika Vitiello (ORCID: https://orcid.org/0000-0001-5383-1295)
- Simon Fürbacher
- JingYe Zhang
- Laura Lange
- Yaqing Zhang
- Andres Jäschke
- Niklas van den Bergh
- Pia Doll
- Murat Sunbul
Institutions
- Heidelberg University (DE)
Publication Details
- Journal
- Journal of the American Chemical Society
- Published
- 2026-01-08
- DOI
- https://doi.org/10.1021/jacs.5c16419
- Citations
- 1
- Primary Topic
- Advanced biosensing and bioanalysis techniques
- Type
- article
- Field-Weighted Citation Impact
- 22.24