Premium
Increasing fluorescence lifetime for resolution improvement in stimulated emission depletion nanoscopy
Author(s) -
Wang LuWei,
Chen Yue,
Yan Wei,
Weng XiaoYu,
Yang ZhiGang,
Ye Tong,
Qu JunLe
Publication year - 2019
Publication title -
journal of biophotonics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.877
H-Index - 66
eISSN - 1864-0648
pISSN - 1864-063X
DOI - 10.1002/jbio.201800315
Subject(s) - sted microscopy , fluorescence , confocal , stimulated emission , microscopy , confocal microscopy , optics , resolution (logic) , materials science , fluorescence lifetime imaging microscopy , fluorescence microscope , temporal resolution , super resolution microscopy , laser , chemistry , physics , artificial intelligence , computer science
Super‐resolution microscopy (SRM) has had a substantial impact on the biological sciences due to its ability to observe tiny objects less than 200 nm in size. Stimulated emission depletion (STED) microscopy represents a major category of these SRM techniques that can achieve diffraction‐unlimited resolution based on a purely optical modulation of fluorescence behaviors. Here, we investigated how the laser beams affect fluorescence lifetime in both confocal and STED imaging modes. The results showed that with increasing illumination time, the fluorescence lifetime in two kinds of fluorescent microspheres had an obvious change in STED imaging mode, compared with that in confocal imaging mode. As a result, the reduction of saturation intensity induced by the increase of fluorescence lifetime can improve the STED imaging resolution at the same depletion power. The phenomenon was also observed in Star635P‐labeled human Nup153 in fixed HeLa cells, which can be treated as a reference for the synthesis of fluorescent labels with the sensitivity to the surrounding environment for resolution improvement in STED nanoscopy.