A novel fluorescence probe, HBTSeSe, was designed and synthesized for the detection of HS with a double-switch mechanism of a broken diselenide bond followed by thiolysis of ether. Then, 2-(2'-hydroxyphenyl)benzothiazole (HBT) was released as fluorophore, which has large Stokes shift based on the excited state intramolecular proton transfer process. The probe responded selectively and rapidly to HS, with the fluorescence increased by 47-fold immediately after the addition of HS. HBTSeSe was able to detect HS in the cytoplasm, specifically in cell imaging experiments. The results also showed that HS was produced in the immune response of RAW264.7 cells activated by phorbol-12-myristate-13-acetate.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648457 | PMC |
http://dx.doi.org/10.1021/acsomega.9b00934 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!