Development of highly sensitive fluorescent probes for the detection of β-galactosidase activity – application to the real-time monitoring of senescence in live cells. Issue 11 (18th May 2018)

• Record Type: Journal Article
• Authors: Safir Filho, Mauro; Dao, Pascal; Gesson, Maéva; Martin, Anthony R.; Benhida, Rachid
• Is Part Of: Analyst. Volume 143:Issue 11(2018)
• Page Start: 2680
• Page End: 2688
• Publication Date: 2018-05-18
• Subjects: Chemistry, Analytic -- Periodicals; 543
• DOI: 10.1039/c8an00516h
• Languages: English
• ISSNs: 0003-2654

Abstract

Abstract : Highly sensitive fluorescent reporters for the detection and monitoring of β-galactosidase activity in live cells. Abstract : We report the development of four novel fluorescent probes to monitor the activity of the β-galactosidase enzyme (β-gal), in vitro and in living cells. The fluorophores are based on a 6-amino-styryl-benzothiazole push–pull core and display a strong ICT emission. The probes encompass the fluorescent motif that is connected to a β-d -galactopyranoside moiety through a self-immolative benzyl carbamate linker (βGal-1–4 ). The screening of four different fluorophores enabled us to access new light-up and two-band ratiometric reporters. The four probes, βGal-1–4, exhibited an extremely fast response and over 200-fold fluorescence enhancement (βGal-1 ) following the enzymatic cleavage of the β-d -galactopyranoside unit. This rapid and extremely sensitive response allowed the detection of senescence-associated β-galactosidase (SA-β-gal) activity; a widely used biomarker of senescence. More importantly, βGal-1 also enabled us to monitor, in real-time, the emergence of senescence in live cells, i.e. the phenotypic transformation from normal to senescent cell. These findings underpin the fact thatβGal-1 may find useful applications in biomedical research. Importantly, βGal-1 is suitable for epifluorescence and confocal microscopies, and flow cytometry techniques, which are among the most common analytical tools in biology.