详细信息

Super-Photostability and Super-Brightness of EC5 Dyes for Super-Resolution Microscopy in the Deep Near-Infrared Spectral Region  ( EI收录)  

文献类型:期刊文献

英文题名:Super-Photostability and Super-Brightness of EC5 Dyes for Super-Resolution Microscopy in the Deep Near-Infrared Spectral Region

作者:Lu, Xicun[1]; Zhuang, Xiaoli[1]; Dong, Yan[1]; Chen, Chong[2]; Wei, Ruwei[1]; Chen, Weichao[1]; Li, Hui[2]; Luo, Xiao[3]; Qian, Xuhong[1,3]; Yang, Youjun[1]

机构:[1] State Key Laboratory of Bioreactor Engineering, Shanghai Key Laboratory of Chemical Biology, School of Pharmacy, East China University of Science and Technology, Shanghai, 200237, China; [2] Jiangsu Key Laboratory of Medical Optics, Suzhou Institute of Biomedical Engineering and Technology, Chinese Academy of Sciences, Suzhou, 215163, China; [3] Shanghai Engineering Research Center of Molecular Therapeutics and New Drug Development, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai, 200241, China

年份:2024

卷号:36

期号:2

起止页码:949

外文期刊名:Chemistry of Materials

收录:EI(收录号:20240215340217)

语种:英文

外文关键词:Diffraction - Infrared devices - Optical resolving power

摘要:The confocal and super-resolution imaging has become routine for the visible spectral region, but not for the deep near-infrared (NIR) region (800-1000 nm) due to the lack of bright and ultraphotostable fluorophores. We devised a premium fluorochromic scaffold (EC5) spectrally active in this region and further optimized it for super-resolution imaging by rational and systematic molecular engineering over the push-pull headgroups. EC5j maximally absorbs/emits at 835/873 nm and offers a superior brightness of 38070 cm-1 M-1 and superior photostability. Using two home-built microscopes with deep-NIR capability, i.e., confocal and structured-illumination microscopes, we demonstrated that super-resolution 2D and 3D-microscopy is now practical with EC5j. In particular, EC5j-adsorbed polystyrene beads furnished a notable spatial resolution of 175 nm with structure-illumination microscopy (SIM) imaging, as compared to the theoretical diffraction limit of 336 nm. Proof-of-concept applications included live-cell confocal imaging of mitophagy, SIM imaging of mitochondria, and deconvolution-based confocal sectioning of cell structures and brain vasculature. The revolutionary expansion of the imaging spectral window brings the field new tools and new insights. ? 2023 American Chemical Society

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