Fluorogenic hydrogen sulfide (H 2 S) donors based on sulfenyl thiocarbonates enable H 2 S tracking and quantification.

Autor: Zhao Y; Department of Chemistry and Biochemistry , Institute of Molecular Biology , Materials Science Institute , University of Oregon , Eugene , OR 97403 , USA . Email: pluth@uoregon.edu., Cerda MM; Department of Chemistry and Biochemistry , Institute of Molecular Biology , Materials Science Institute , University of Oregon , Eugene , OR 97403 , USA . Email: pluth@uoregon.edu., Pluth MD; Department of Chemistry and Biochemistry , Institute of Molecular Biology , Materials Science Institute , University of Oregon , Eugene , OR 97403 , USA . Email: pluth@uoregon.edu.
Jazyk: angličtina
Zdroj: Chemical science [Chem Sci] 2018 Dec 10; Vol. 10 (6), pp. 1873-1878. Date of Electronic Publication: 2018 Dec 10 (Print Publication: 2019).
DOI: 10.1039/c8sc05200j
Abstrakt: Hydrogen sulfide (H 2 S) is an important cellular signaling molecule that exhibits promising protective effects. Although a number of triggerable H 2 S donors have been developed, spatiotemporal feedback from H 2 S release in biological systems remains a key challenge in H 2 S donor development. Herein we report the synthesis, evaluation, and application of caged sulfenyl thiocarbonates as new fluorescent H 2 S donors. These molecules rely on thiol cleavage of sulfenyl thiocarbonates to release carbonyl sulfide (COS), which is quickly converted to H 2 S by carbonic anhydrase (CA). This approach is a new strategy in H 2 S release and does not release electrophilic byproducts common from COS-based H 2 S releasing motifs. Importantly, the release of COS/H 2 S is accompanied by the release of a fluorescent reporter, which enables the real-time tracking of H 2 S by fluorescence spectroscopy or microscopy. Dependent on the choice of fluorophore, either one or two equivalents of H 2 S can be released, thus allowing for the dynamic range of the fluorescent donors to be tuned. We demonstrate that the fluorescence response correlates directly with quantified H 2 S release and also demonstrate the live-cell compatibility of these donors. Furthermore, these fluorescent donors exhibit anti-inflammatory effects in RAW 264.7 cells, indicating their potential application as new H 2 S-releasing therapeutics. Taken together, sulfenyl thiocarbonates provide a new platform for H 2 S donation and readily enable fluorescent tracking of H 2 S delivery in complex environments.
Databáze: MEDLINE