Analytical Chemistry · 2014 · 51 citations · 20 references
EngineeringTurn-on Fluorescent ProbeRedox BiologyLow Probe/thiol RatioBioanalysisCellular ImagingMolecular ImagingBiophysicsNovel Imaging MethodBiochemistryFluorescence ImagingExtant ProbesSingle-molecule DetectionFluorescence MicroscopyBiomedical ImagingBiologically Significant ThiolsChemical ProbeHigh Probe/thiol RatioMedicineCell ImagingHigh-throughput ScreeningDrug Analysis
There is a very limited number of existing probes whose fluorescence is turned on in the presence of the class of biological thiols made up of glutathione, cysteine, and homocysteine. The extant probes for this class of biological thiols commonly have poor aqueous solubility and long analyte response times, and they demand a very high probe/thiol ratio for decreased time of significant reporter signal generation; knowledge regarding their selectivity with respect to other sulfur-based analytes is unclear. Described here is a previously unreported photoinduced electron-transfer-quenched probe (HMBQ-Nap 1) that offers highly selective and rapid in vitro detection of this class of biologically important thiols at low concentrations and low probe/thiol ratio, and importantly, very rapid imaging of these biological thiols in human cells.
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Reaction Based Fluorescent Probes for Hydrogen Sulfide
Chunrong Liu, Bo Peng, Li Sheng et al. · Organic Letters · 2012 · 222 citations · Full text
Ratiometric Fluorescence Imaging of Cellular Glutathione
Gun-Joong Kim, Ki‐Won Lee, Hyockman Kwon et al. · Organic Letters · 2011 · 215 citations
Fluorescence Microscopy, Ratiometric Fluorescence Imaging, Tissue Imaging +15