Send to

Choose Destination
ACS Chem Biol. 2017 Aug 18;12(8):2117-2123. doi: 10.1021/acschembio.7b00279. Epub 2017 Jun 30.

Inhibition of Mitochondrial Bioenergetics by Esterase-Triggered COS/H2S Donors.

Author information

Department of Chemistry and Biochemistry, Materials Science Institute, Institute of Molecular Biology, University of Oregon , Eugene, Oregon 97403, United States.
Department of Anaesthesiology, University of Texas Medical Branch , Galveston, Texas 77555, United States.


Hydrogen sulfide (H2S) is an important biological mediator, and synthetic H2S donating molecules provide an important class of investigative tools for H2S research. Here, we report esterase-activated H2S donors that function by first releasing carbonyl sulfide (COS), which is rapidly converted to H2S by the ubiquitous enzyme carbonic anhydrase (CA). We report the synthesis, self-immolative decomposition, and H2S release profiles of the developed scaffolds. In addition, the developed esterase-triggered COS/H2S donors exhibit higher levels of cytotoxicity than equivalent levels of Na2S or the common H2S donors GYY4137 and AP39. Using cellular bioenergetics measurements, we establish that the developed donors reduce cellular respiration and ATP synthesis in BEAS 2B human lung epithelial cells, which is consistent with COS/H2S inhibition of cytochrome c oxidase in the mitochondrial respiratory chain although not observed with common H2S donors at the same concentrations. Taken together, these results may suggest that COS functions differently than H2S in certain biological contexts or that the developed donors are more efficient at delivering H2S than other common H2S-releasing motifs.

[Indexed for MEDLINE]
Free PMC Article

Supplemental Content

Full text links

Icon for American Chemical Society Icon for PubMed Central
Loading ...
Support Center