TY - JOUR
T1 - A novel ratiometric fluorescent probe with high selectivity for lysosomal nitric oxide imaging
AU - Xu, Zhiling
AU - Liu, Songtao
AU - Xu, Liren
AU - Li, Zichun
AU - Zhang, Xiaoli
AU - Kang, Hao
AU - Liu, Yifan
AU - Yu, Jin
AU - Jing, Jing
AU - Niu, Guangle
AU - Zhang, Xiaoling
N1 - Publisher Copyright:
© 2024
PY - 2024/4/8
Y1 - 2024/4/8
N2 - Nitric oxide (NO) plays critical roles in both physiology and pathology, serving as a significant signaling molecule. Recent investigations have uncovered the pivotal role of lysosome as a critical organelle where intracellular NO exists and takes function. In this study, we developed a novel ratiometric fluorescent probe called XL-NO and modified it with a morpholine unit, which followed the intramolecular charge transfer (ICT) mechanism. The probe could detect lysosomal nitric oxide with high selectivity and sensitivity. The probe XL-NO contained a secondary amine moiety that could readily react with NO in lysosomes, leading to the formation of the N-nitrosation product. The N-nitroso structure enhanced the capability in push-pull electron, which obviously led to the change of fluorescence from 621 nm to 521 nm. In addition, XL-NO was discovered to have some evident advantages, such as significant ratiometric signal (I521/I621) change, strong anti-interference ability, good biocompatibility, and a low detection limit (LOD = 44.3 nM), which were crucial for the detection of lysosomal NO. To evaluate the practical application of XL-NO, NO imaging experiments were performed in both living cells and zebrafish. The results from these experiments confirmed the feasibility and reliability of XL-NO for exogenous/endogenous NO imaging and lysosome targeting.
AB - Nitric oxide (NO) plays critical roles in both physiology and pathology, serving as a significant signaling molecule. Recent investigations have uncovered the pivotal role of lysosome as a critical organelle where intracellular NO exists and takes function. In this study, we developed a novel ratiometric fluorescent probe called XL-NO and modified it with a morpholine unit, which followed the intramolecular charge transfer (ICT) mechanism. The probe could detect lysosomal nitric oxide with high selectivity and sensitivity. The probe XL-NO contained a secondary amine moiety that could readily react with NO in lysosomes, leading to the formation of the N-nitrosation product. The N-nitroso structure enhanced the capability in push-pull electron, which obviously led to the change of fluorescence from 621 nm to 521 nm. In addition, XL-NO was discovered to have some evident advantages, such as significant ratiometric signal (I521/I621) change, strong anti-interference ability, good biocompatibility, and a low detection limit (LOD = 44.3 nM), which were crucial for the detection of lysosomal NO. To evaluate the practical application of XL-NO, NO imaging experiments were performed in both living cells and zebrafish. The results from these experiments confirmed the feasibility and reliability of XL-NO for exogenous/endogenous NO imaging and lysosome targeting.
KW - Biological imaging
KW - Lysosomes-targeted
KW - Nitric oxide
KW - Ratiometric fluorescent probe
KW - Zebrafish
UR - http://www.scopus.com/inward/record.url?scp=85185829836&partnerID=8YFLogxK
U2 - 10.1016/j.aca.2024.342303
DO - 10.1016/j.aca.2024.342303
M3 - Article
C2 - 38438223
AN - SCOPUS:85185829836
SN - 0003-2670
VL - 1297
JO - Analytica Chimica Acta
JF - Analytica Chimica Acta
M1 - 342303
ER -