扫描电镜
荧光
生物物理学
罗丹明
生物相容性
共焦显微镜
显微镜
荧光显微镜
化学
荧光团
纳米技术
材料科学
生物
细胞生物学
受激发射
物理
光学
有机化学
激光器
量子力学
作者
Jonas Bucevičius,Rūta Gerasimaitė,Kamila A. Kiszka,Shalini Pradhan,Georgij Kostiuk,Tanja Koenen,Gražvydas Lukinavičius
标识
DOI:10.1038/s41467-023-36913-2
摘要
Abstract The development of live-cell fluorescence nanoscopy is powered by the availability of suitable fluorescent probes. Rhodamines are among the best fluorophores for labeling intracellular structures. Isomeric tuning is a powerful method for optimizing the biocompatibility of rhodamine-containing probes without affecting their spectral properties. An efficient synthesis pathway for 4-carboxyrhodamines is still lacking. We present a facile protecting-group-free 4-carboxyrhodamines’ synthesis based on the nucleophilic addition of lithium dicarboxybenzenide to the corresponding xanthone. This approach drastically reduces the number of synthesis steps, expands the achievable structural diversity, increases overall yields and permits gram-scale synthesis of the dyes. We synthesize a wide range of symmetrical and unsymmetrical 4-carboxyrhodamines covering the whole visible spectrum and target them to multiple structures in living cells – microtubules, DNA, actin, mitochondria, lysosomes, Halo-tagged and SNAP-tagged proteins. The enhanced permeability fluorescent probes operate at submicromolar concentrations, allowing high-contrast STED and confocal microscopy of living cells and tissues.
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