Photoconversion of fluorescent proteins by blue and complementary near-infrared light, termed primed conversion (PC), is a mechanism recently discovered for Dendra2. We demonstrate that controlling the conformation of arginine at residue 66 by threonine at residue 69 of fluorescent proteins from Anthozoan families (Dendra2, mMaple, Eos, mKikGR, pcDronpa protein families) represents a general route to facilitate PC. Mutations of alanine 159 or serine 173, which are known to influence chromophore flexibility and allow for reversible photoswitching, prevent PC. In addition, we report enhanced photoconversion for pcDronpa variants with asparagine 116. We demonstrate live-cell single-molecule imaging with reduced phototoxicity using PC and record trajectories of RNA polymerase in Escherichia coli cells.

Super-resolution fluorescence microscopy plays a major role in revealing the organization and dynamics of living cells. Nevertheless, single-molecule localization microscopy imaging of multiple targets is still limited by the availability of suitable fluorophore combinations. Here, we introduce a novel imaging strategy which combines primed photoconversion (PC) and UV-photoactivation for imaging different molecular species tagged by suitable fluorescent protein combinations. In this approach, the fluorescent proteins can be specifically photoactivated/-converted by different light wavelengths using PC and UV-activation modes but emit fluorescence in the same spectral emission channel. We demonstrate that this aberration-free, live-cell compatible imaging method can be applied to various targets in bacteria, yeast and mammalian cells and can be advantageously combined with correlative imaging schemes.

Precise drift correction is crucial for every single-molecule localization-based microscopy experiment. We evaluate commonly used fiducial markers such as gold nanoparticles, TetraSpeck microspheres, FluoSpheres and nanodiamonds. We introduce spectrally red-shifted fluorescent particles as optimal fiducial markers. Our concept exploits exciting the fluorescent particles at low efficiency far away from their absorption maximum. A fluorescent particle that is covered by a multitude of dyes will nevertheless yield a bright fiducial signal. This represents a simple yet powerful approach to alleviate common problems in drift corrections caused by photobleaching, sudden signal intensity changes or saturation effects of fiducial markers. We adapt our approach for PALM, sptPALM and DNA-PAINT experiments and demonstrate its simple use for varying imaging conditions in different spectral channels.