Related Experiment Video
Updated: Aug 6, 2026

Visualizing Intracellular SNARE Trafficking by Fluorescence Lifetime Imaging Microscopy
Published on: December 29, 2017
Intrinsic Fluorescence Fluctuations of Large Stokes Shift Fluorescent Proteins: LSSmOrange and mKeima Studied by
Sandeep Yadav1, Bidyut Sarkar1,2, Yuna Kinoshita3
1Molecular Spectroscopy Laboratory, RIKEN, 2-1 Hirosawa, Wako351-0198, Japan.
Abstract:
Large Stokes shift fluorescent protein (LSS FP) is a promising tool for biological research that is compatible with a broad range of advanced microscopy techniques. Here, we have investigated the ground-state heterogeneity and dynamics of two LSS FPs, LSSmOrange and mKeima, by two-dimensional fluorescence lifetime correlation spectroscopy. Both LSS FPs were found to have two states with distinct mean fluorescence lifetimes. From the pH-dependent change of relative populations, the states with short and long fluorescence lifetimes were assigned to the cis- and trans- forms of the chromophore, respectively. These states showed interconversion on two distinct time scales, submicroseconds to a few microseconds and submilliseconds to milliseconds. Excitation-power dependence and the symmetry of cross-correlations indicated that while the microsecond dynamics is thermally induced, the slow submillisecond dynamics is an irreversible photoinduced process. The knowledge obtained is expected to be helpful in the spectroscopic and imaging applications of LSS FPs.
Related Concept Videos
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...
Super-resolution Fluorescence Microscopy

