| Literature DB >> 26381762 |
Wei Chen1, Ethan W Rosser1, Tetsuro Matsunaga2, Armando Pacheco1, Takaaki Akaike2, Ming Xian3.
Abstract
Endogenous hydrogen polysulfides (H2Sn; n>1) have been recognized as important regulators in sulfur-related redox biology. H2Sn can activate tumor suppressors, ion channels, and transcription factors with higher potency than H2S. Although H2Sn are drawing increasing attention, their exact mechanisms of action are still poorly understood. A major hurdle in this field is the lack of reliable and convenient methods for H2Sn detection. Herein we report a H2Sn-mediated benzodithiolone formation under mild conditions. This method takes advantage of the unique dual reactivity of H2Sn as both a nucleophile and an electrophile. Based on this reaction, three fluorescent probes (PSP-1, PSP-2, and PSP-3) were synthesized and evaluated. Among the probes prepared, PSP-3 showed a desirable off/on fluorescence response to H2Sn and high specificity. The probe was successfully applied in visualizing intracellular H2Sn.Entities:
Keywords: cyclization; fluorescence; fluorescent probes; hydrogen polysulfides; imaging agents
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Year: 2015 PMID: 26381762 PMCID: PMC4715616 DOI: 10.1002/anie.201506887
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336