CO-releasing molecule-3
(CORM-3), mainly metal carbonyl compounds,
is widely used as experimental tools to deliver CO, a biological “gasotransmitter”,
in mammalian systems. CORM-3 is also proposed as a potential new antimicrobial
agent, which kills bacteria effectively and rapidly in vitro and in
animal models. Organelle-targeting therapy, as a highly effective
therapeutic strategy with little toxic and side effects, has important
research significance and development prospects. Therefore, the development
of effective methods for detecting and tracking CORM-3 at the subcellular
level has important implications. In this paper, an easily available
Golgi-targetable fluorescent probe (Golgi-Nap-CORM-3) was proposed
for CORM-3 detection. In the probe Golgi-Nap-CORM-3, the phenyl sulfonamide
group was selected as the Golgi-targetable unit, naphthalimide dye
was chosen as a fluorophore, and the nitro group was selected as a
CORM-3-responsive unit. Golgi-Nap-CORM-3 shows a CORM-3-reponsive
increase of fluorescence emission at 520 nm. Using the excellent probe,
the change of CORM-3 in HeLa cells, HepG2 cells, and zebrafish is
successfully monitored. This study demonstrates very important information
for the study of CORM-3 in vivo systems.