Phototriggered Hydrogen Persulfide Donors via Hydrosulfide Radical Formation Enhancing the Reactive Sulfur Metabolome in Cells.

Hydrogen persulfide (HS) is an important sulfur-containing signaling molecule that plays a crucial role in the homeostasis of various organ systems, such as the renal, cardiovascular, liver, and gastrointestinal systems. However, research on HS in biological settings is still challenging due to its instability and high reactivity. Compounds that can controllably release HS (also known as donors) are thus crucial research tools. Currently, available HS donors are still very limited, with most of them relying on modified disulfide templates. These templates possess an unavoidable limitation of being susceptible to cellular disulfide exchange which can compromise their efficacy. In this work, we explored nondisulfide-based and nonoxidation-dependent templates for the design of HS donors. We found that tertiary naphthacyl thiols could undergo phototriggered C-S homolytic cleavage to form HS via hydrosulfide (HS) radicals. In addition, the release of HS was associated with the formation of a product with strong blue fluorescence, which allowed for real-time monitoring of the release process. This reaction was demonstrated to proceed effectively in both buffers and cells, with the ability to enhance intracellular production of persulfides, including GSSH, CysSSH, HS, HS, etc. It provides a unique photocontrolled HS donor system with distinct advantages compared to known HS donors due to its good stability and spatiotemporal control ability.