Related Experiment Video
Updated: Apr 26, 2026

Automated Two-dimensional Spatiotemporal Analysis of Mobile Single-molecule FRET Probes
Published on: November 23, 2021
RuNH2@AuNPs as two-photon luminescent probes for thiols in living cells and tissues
Pingyu Zhang1, Jinquan Wang1, Huaiyi Huang1
1MOE Laboratory of Bioinorganic and Synthetic Chemistry, State Key Laboratory of Optoelectronic Materials and Technologies, School of Chemistry and Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275, PR China.
Abstract:
Two-photon luminescent sensors have emerged as promising molecular tools for imaging biomolecules in living systems. Here, we present hybrid gold nanocomposites RuNH2@AuNPs as luminescence off-on probes in response to thiols, which can replace the Ru(II) complexes on the surfaces of the AuNPs to release the luminophore RuNH2. The liberated Ru(II) complexes exhibit strong two-photon luminescence and a large two-photon absorption cross section by using the two-photon excitation wavelength at 800 nm. Furthermore, the probe responses toward thiols with high selectivity and insensitivity to pH over the biologically relevant pH range. This two-photon probe can visualize biological thiols levels in live cells as well as in living mouse tissues at depths of 80-170 μm by two-photon microscopy.
More Related Videos
05:45In Vivo Two-Color 2-Photon Imaging of Genetically-Tagged Reporter Cells in the Skin
Published on: July 11, 2019
10:04Imaging Amyloid Tissues Stained with Luminescent Conjugated Oligothiophenes by Hyperspectral Confocal Microscopy and Fluorescence Lifetime Imaging
Published on: October 20, 2017
Related Concept Videos
Labeling DNA Probes
Radioisotopes, fluorophores, or small molecule binding partners like biotin or digoxigenin, are the most widely used reporter tags for labeling DNA probes. These labels can be attached to the probe DNA molecule via...
Photoluminescence: Applications
Protein Dynamics in Living Cells
Fluorescent recovery after photobleaching (FRAP) is a fluorescent-protein-based detection technique used to quantify protein movement rates within the cell. This method exposes a small portion of the cell to an intense laser beam. The laser beam causes permanent photobleaching of the fluorophore-tagged proteins in the exposed region. As the bleached...