Sequential detection of H2S and HOBr with a novel lysosome-targetable fluorescent probe and its application in biological imaging

被引:21
|
作者
Mu, Shuai [1 ,2 ]
Zhang, Jinlong [1 ,2 ]
Gao, Hong [1 ,2 ]
Wang, Yaya [1 ,2 ]
Rizvi, Syed Faheem Askari [1 ,2 ]
Ding, Nana [3 ]
Liu, Xiaoyan [1 ,2 ]
Wu, Lan [3 ]
Zhang, Haixia [1 ,2 ]
机构
[1] Lanzhou Univ, State Key Lab Appl Organ Chem, Key Lab Nonferrous Met Chem & Resources Utilizat, Lanzhou 730000, Peoples R China
[2] Lanzhou Univ, Coll Chem & Chem Engn, Lanzhou 730000, Peoples R China
[3] Northwest Minzu Univ, Coll Chem Engn, Lanzhou 730030, Gansu, Peoples R China
基金
中国国家自然科学基金;
关键词
Fluorescent probe; Sequential response; Hydrogen sulfide; Hypobromous acid; Cell imaging; HYDROGEN-SULFIDE; OXIDATIVE STRESS; CELLS; DISEASE; ACID; MYELOPEROXIDASE; INHIBITOR; MECHANISM; VIVO;
D O I
10.1016/j.jhazmat.2021.126898
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Understanding the complex relationship between active small molecules is of great significance in various physiological processes. Herein, we present the design and synthesis of a sequential responsive Lysosome-Naphthalene imide-Azido (lyso-NP-N-3) reporter for probing the H2S and HOBr within organelle (lysosome) in living cells. Probe lyso-NP-N-3 exhibited high selectivity and sensitivity towards H2S (LOD = 23.5 nM) and HOBr (LOD = 254 nM). Additionally, lyso-NP-N-3 possessed an excellent lysosome targeting ability and was utilized to visualize the exogenous/endogenous H2S and HOBr in RAW 264.7, Hela and HepG2 cells. Facilitated by this sequentially activated mechanism, the probe was successfully applied to confirm that the reported scavenger of HOBr, N-acetyl-L-cysteine (NAC) mainly relied on its metabolite H2S to eliminate excess HOBr, thereby playing the role of cell regulation and protection. These results establish the crosstalk between H2S and HOBr in lysosome and provide a promising tool to study metabolite interactions.
引用
收藏
页数:9
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