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Direct detection of nitroxyl in aqueous solution using a tripodal copper(II) BODIPY complex.

ABSTRACT: The synthesis, photophysical properties, and a biological application of BODIPY-triazole 1 (BOT1) are described. BOT1 juxtaposes a BODIPY fluorophore with a tripodal ligand platform via a triazole bridge. The triazole linker is afforded by azide-alkyne "click" chemistry and comprises the third arm of the tripodal architecture. BOT1 binds Cu(2+) in aqueous solution to form a Cu(II)[BOT1] complex in which emission from the BODIPY moiety is efficiently quenched. This complex exhibits a prompt turn-on response when exposed to nitroxyl, and this emission response is specific to HNO over other reactive nitrogen and oxygen species. Notably, Cu(II)[BOT1] does not fluoresce in the presence of nitric oxide, making this system the first discrete molecular probe capable of detecting HNO over NO under physiologically relevant conditions. Fluorescence microscopy experiments establish that Cu(II)[BOT1] is membrane-permeable and can successfully signal the presence of HNO in live cells.

SUBMITTER: Rosenthal J

PROVIDER: S-EPMC2866442 | biostudies-other | 2010 Apr

REPOSITORIES: biostudies-other

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Direct detection of nitroxyl in aqueous solution using a tripodal copper(II) BODIPY complex.

Rosenthal Joel J Lippard Stephen J SJ

Journal of the American Chemical Society 20100401 16

The synthesis, photophysical properties, and a biological application of BODIPY-triazole 1 (BOT1) are described. BOT1 juxtaposes a BODIPY fluorophore with a tripodal ligand platform via a triazole bridge. The triazole linker is afforded by azide-alkyne "click" chemistry and comprises the third arm of the tripodal architecture. BOT1 binds Cu(2+) in aqueous solution to form a Cu(II)[BOT1] complex in which emission from the BODIPY moiety is efficiently quenched. This complex exhibits a prompt turn- ...[more]

PMID: 20355724

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