Abstract
In fluctuation-based optical nanoscopy, investigating high-density labeled subcellular structures with high fidelity has been a significant challenge. In this study, based on super-resolution radial fluctuation (SRRF) microscopy, the joint tagging (JT) strategy is employed to enable fast high-density nanoscopic imaging and tracking. In fixed cell experiment, multiple types of quantum dots with distinguishable fluorescence spectra are jointly tagged to subcellular microtubules. In each spectral channel, the decrease in labeling density guarantees the high-fidelity super-resolution reconstruction using SRRF microscopy. Subsequently, the combination of all spectral channels achieves high-density super-resolution imaging of subcellular microtubules with a resolution of ~62 nm using JT assisted SRRF technique. In the live-cell experiment, 3-channel JT is utilized to track the dynamic motions of high-density toxin-induced lipid clusters for 1 minute, achieving the simultaneous tracking of many individual toxin-induced lipid clusters spatially distributed significantly below the optical diffraction limit in living cells.