A mitochondria-targeted chemiluminescent probe for detection of hydrogen sulfide in cancer cells, human serum and in vivo

被引:4
|
作者
Gunduz, Hande [1 ,2 ]
Almammadov, Toghrul [2 ]
Dirak, Musa [2 ]
Acari, Alperen [3 ]
Bozkurt, Berkan [3 ,4 ]
Kolemen, Safacan [2 ,3 ,5 ]
机构
[1] Koc Univ, Nanofabricat & Nanocharacterizat Ctr Sci & Technol, TR-34450 Istanbul, Turkiye
[2] Koc Univ, Dept Chem, Rumelifeneri Yolu, TR-34450 Istanbul, Turkiye
[3] Koc Univ Res Ctr Translat Med KUTTAM, TR-34450 Istanbul, Turkiye
[4] Koc Univ, Grad Sch Hlth Sci, Rumelifeneri Yolu, TR-34450 Istanbul, Turkiye
[5] Koc Univ Surface Sci & Technol Ctr KUYTAM, TR-34450 Istanbul, Turkiye
来源
RSC CHEMICAL BIOLOGY | 2023年 / 4卷 / 09期
关键词
FLUORESCENT-PROBES; SIGNALING MOLECULE; OXIDATIVE STRESS; PROLIFERATION; H2S; METABOLISM; SYNTHASE; BIOLOGY; ROLES;
D O I
10.1039/d3cb00070b
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hydrogen sulfide (H2S) as a critical messenger molecule plays vital roles in regular cell function. However, abnormal levels of H2S, especially mitochondrial H2S, are directly correlated with the formation of pathological states including neurodegenerative diseases, cardiovascular disorders, and cancer. Thus, monitoring fluxes of mitochondrial H2S concentrations both in vitro and in vivo with high selectivity and sensitivity is crucial. In this direction, herein we developed the first ever example of a mitochondria-targeted and H2S-responsive new generation 1,2-dioxetane-based chemiluminescent probe (MCH). Chemiluminescent probes offer unique advantages compared to conventional fluorophores as they do not require external light irradiation to emit light. MCH exhibited a dramatic turn-on response in its luminescence signal upon reacting with H2S with high selectivity. It was used to detect H2S activity in different biological systems ranging from cancerous cells to human serum and tumor-bearing mice. We anticipate that MCH will pave the way for development of new organelle-targeted chemiluminescence agents towards imaging of different analytes in various biological models.
引用
收藏
页码:675 / 684
页数:11
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