Intracellular redox homeostasis is highly important for
the physiological
processes of living organisms. Real-time monitoring of the dynamics
of this intracellular redox process is pivotal but challenging because
the biological redox reactions involved in the process are reversible
and require at least one pair of oxidizing and reducing species. Thus,
biosensors for investigating intracellular redox homeostasis need
to be dual-functional, reversible, and, ideally, ratiometric in order
for them to have real-time monitoring capacity and to provide accurate
imaging information. In light of the importance of the redox pair
between ClO– and GSH in living organisms, herein,
we used the phenoselenazine (PSeZ) moiety as an electron donor and
a reaction site to design a coumarin-based fluorescent probe, PSeZ-Cou-Golgi. After successive treatment with ClO– and GSH, the probe PSeZ-Cou-Golgi experienced an oxidation
of selenium (Se) to selenoxide (SeO) by ClO– and a subsequent reduction of SeO to Se by GSH. The redox
reactions alternatively changed the electron-donating strength of
the donor in the probe PSeZ-Cou-Golgi, in turn affecting
the intramolecular charge transfer process that resulted in the reversible,
ratiometric change of fluorescence from red to green. After four cycles
of reversible ClO–/GSH detection during in vitro experiments, the probe PSeZ-Cou-Golgi still had good performance. With the Golgi-targeting group, the
probe PSeZ-Cou-Golgi was able to monitor the dynamic
change of the ClO–/GSH-mediated redox state during
Golgi oxidative stress, making it a versatile molecular tool. More
importantly, the probe PSeZ-Cou-Golgi could facilitate
the imaging of the dynamic redox state during acute lung injury progression.