Quantitative Monitoring and Visualization of Hydrogen Sulfide In Vivo Using a Luminescent Probe Based on a Ruthenium(II) Complex.
Zhongbo DuBo SongWenzhu ZhangChengchen DuanYong-Lei WangChaolong LiuRun ZhangJingli YuanPublished in: Angewandte Chemie (International ed. in English) (2018)
Development of novel bioanalytical methods for monitoring of H2 S is key toward understanding the physiological and pathological functions of this gasotransmitter in live organisms. A ruthenium(II)-complex-based luminescence probe, Ru-MDB (MDB: 4'-methyl-[2,2'-bipyridine]-4-yl)methyl 2-((2,4-dinitrophenyl)thio)benzoate), was developed by introducing a new H2 S responsive masking moiety to a red-emitting RuII luminophore. Cleavage of this masking group by a H2 S-triggered reaction leads to a luminescence "off-on" response. The long-lived emissions of Ru-MDB and its reaction product with H2 S allowed quantitative detection of H2 S in autofluorescence-rich human sera and adult zebrafish organs using the time-gated luminescence mode. Ru-MDB exhibits red emission, a large Stokes shift, high specificity and sensitivity for H2 S detection, and low cytotoxicity, which enables imaging and flow cytometry analysis of lysosomal H2 S generation in live inflamed cells under drug stimulation. Monitoring of H2 S in live Daphnia magna, zebrafish embryos, adult zebrafish, and mice, was conducted by in vivo imaging using Ru-MDB as a probe.
Keyphrases
- energy transfer
- quantum dots
- high resolution
- flow cytometry
- sensitive detection
- living cells
- loop mediated isothermal amplification
- induced apoptosis
- endothelial cells
- fluorescent probe
- label free
- cancer therapy
- cell cycle arrest
- young adults
- emergency department
- mass spectrometry
- cell death
- skeletal muscle
- oxidative stress
- childhood cancer
- drug delivery
- insulin resistance
- signaling pathway
- single molecule
- transcription factor
- light emitting
- metal organic framework
- municipal solid waste