Development of ultrafast camera-based single fluorescent-molecule imaging for cell biology.
Ontology highlight
ABSTRACT: The spatial resolution of fluorescence microscopy has recently been greatly enhanced. However, improvements in temporal resolution have been limited, despite their importance for examining living cells. Here, we developed an ultrafast camera system that enables the highest time resolutions in single fluorescent-molecule imaging to date, which were photon-limited by fluorophore photophysics: 33 and 100 µs with single-molecule localization precisions of 34 and 20 nm, respectively, for Cy3, the optimal fluorophore we identified. Using theoretical frameworks developed for the analysis of single-molecule trajectories in the plasma membrane (PM), this camera successfully detected fast hop diffusion of membrane molecules in the PM, previously detectable only in the apical PM using less preferable
SUBMITTER: Fujiwara TK
PROVIDER: S-EPMC10244617 | biostudies-literature | 2023 Aug
REPOSITORIES: biostudies-literature
ACCESS DATA