Abstract
Cell-permeable rhodamine dyes are reductively quenched by NaBH4 into a non-fluorescent leuco-rhodamine form. Quenching is reversible, and their fluorescence is recovered when the dyes are oxidized. In living cells, oxidation occurs spontaneously, and can result in up to ten-fold higher densities of single molecule localizations, and more photons per localization as compared with unmodified dyes. These two parameters directly impact the achievable resolution, and we see a significant improvement in the quality of live-cell point-localization super-resolution images taken with reduced dyes. These improvements carry over to increase the density of trajectories for single-molecule tracking experiments.
| Original language | English |
|---|---|
| Pages (from-to) | 750-755 |
| Number of pages | 6 |
| Journal | ChemPhysChem |
| Volume | 15 |
| Issue number | 4 |
| DOIs | |
| State | Published - Mar 17 2014 |
Keywords
- fluorophores
- live-cell imaging
- rhodamine
- single-molecule studies
- superresolution microscopy
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