Development of fluorescent dual-FRET probe for simultaneous detection of caspase-8 and caspase-9 activities and their relative quantification

A multi-FRET three-fluorophore probe containing coumarin, fluorescein and rhodamine B with two enzymati-cally cleavable linkers has been synthesized and optimized for the simultaneous activity detection and relative quantification of two proteases - caspase-8 and caspase-9. The probe designed as a ratiometric single-excitation triple-emission system shows specific change in fluorescence intensities upon enzymatic cleavage of individual linkers in model mixtures as well as in a cell lysate. The activation of caspase-8 and caspase-9 is responsible for initiation of extrinsic or intrinsic apoptotic pathway, respectively, and the probe was proposed as a single chemical tool which could help to decipher a mechanism of cell death induced by various stimuli. The main advantage of this probe is the simplicity of its preparation using conventional organic synthesis, easy application for measurement and evaluation of the results.

Automated summary

A multi-FRET three-fluorophore probe has been synthesized and optimized for the simultaneous activity detection and quantification of two proteases. The probe shows specific fluorescence intensity changes upon enzymatic cleavage, making it a potential tool for studying cell death mechanisms.