Abstract

Hypochlorous acid (HClO) plays a vital role in the immune system and is involved in various human diseases. To fully understand its biological functions in cellular signaling pathways, apoptosis and human diseases, effective chemical tools for directly tracing HClO at subcellular levels are greatly demanded. Herein, two mitochondria- and lysosome-targetable luminescent β-diketonate–Eu 3+ complexes, Mito-BHHBCB-Eu 3+ and Lyso-BHHBCB-Eu 3+ , were developed as probes for the time-gated luminescence detection of HClO inside mitochondria and lysosomes of living cells, respectively. The probes were designed by incorporating a mitochondria-anchoring (triphenylphosphonium) motif or a lysosome-anchoring (morpholine) motif with a strongly luminescent HOCl-responsive β-diketonate–Eu 3+ complex, BHHBCB-Eu 3+ , to ensure the probe molecules to be driven into mitochondria or lysosomes for responding to HOCl therein. Upon exposure to HClO, the probes exhibited a fast luminescence response (within 5 s) towards HClO with good selectivity and high sensitivity (<15 nM). In live cell experiments, both probes, Mito-BHHBCB-Eu 3+ and Lyso-BHHBCB-Eu 3+ , were successfully located in the corresponding organelles as expected, which enabled exogenous and endogenous HClO to be imaged at subcellular levels. Taking advantages of time-gated luminescence bioimaging technique, the uptake of exogenous HClO by Daphnia magna was also successfully imaged by time-gated luminescence microscopy. The results reveal that Mito-BHHBCB-Eu 3+ and Lyso-BHHBCB-Eu 3+ could serve as useful tools for real-time imaging of HClO at subcellular levels and in vivo with high specificity and contrast.