生物正交化学
铱
标签
磷光
化学
纳米技术
组合化学
荧光
点击化学
材料科学
生物化学
催化作用
物理
量子力学
作者
Peiling Dai,Chuanjin Luo,Zhiqi Xu,S. S. Sun,Yuyang Tian,Kenneth Yin Zhang,Kenneth Kam‐Wing Lo,Shujuan Liu,Wei Huang,Huan Wang,Qiang Zhao
标识
DOI:10.1002/ange.202504230
摘要
Fluorogenic bioorthogonal probes are crucial tools in biomedical research, which enables non‐invasive wash‐free imaging of specific biomolecules in living systems. Lifetime‐responsive bioorthogonal probes represent another promising and attractive alternative, offering the potential for real‐time wash‐free visualization of bioorthogonal labelling processes via photoluminescence lifetime imaging microscopy (PLIM). However, their widespread application is limited by the lack of suitable lifetime‐responsive probes. Herein, a series of phosphorescent iridium(III) phenanthrolinedione complexes were reported. Intriguingly, upon bioorthogonal reaction with an α‐angelica lactone derivative, the complexes exhibited remarkable emission responses in three distinct manners, which were found to correlate with the different emissive excited states of the complexes. Crucially, two of the complexes maintained similar emission intensity but exhibited significant emission lifetime elongation during labelling reactions, which facilitated simultaneous and discriminative visualization of the reacted and unreacted probes in cellular imaging without the need for washing steps. One of the complexes was used for organelle targeting and specific protein labelling through bioorthogonal reactions in living cells. The intracellular probe transportation and labelling dynamics were visualized and analyzed using PLIM. This work highlights the unique potential of lifetime‐responsive iridium(III) complexes as powerful chemical tools for live‐cell imaging and unveiling the spatiotemporal dynamics of biomolecules during bioorthogonal reactions.
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