A fluorescent light-up probe based on AIE and ESIPT processes for β-galactosidase activity detection and visualization in living cells

Lu Peng, Meng Gao, Xiaolei Cai, Ruoyu Zhang, Kai Li, Guangxue Feng, Aijun Tong*, Bin Liu

*Corresponding author for this work

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Abstract

A novel fluorescent probe SA-βGal is reported here with light-up response to β-galactosidase. SA-βGal possesses the β-galactopyranoside group to react with β-galactosidase and releases the fluorescent salicylaldehyde azine with both aggregation induced emission (AIE) and excited-state intramolecular proton transfer (ESIPT) characteristics. The linear fluorescent response enables the in vitro quantification of β-galactosidase activity in a range of 0-0.1 U mL-1 with a detection limit of 0.014 U mL-1. The probe exhibits significant advantages, such as no self-quenching at high concentrations, a large Stokes shift (190 nm) and high specificity to β-galactosidase with an excellent light-up ratio of 820 fold. Moreover, thanks to its good retention in living cells, the application of SA-βGal for the imaging of cellular β-galactosidase was also achieved with high contrast.

Original languageEnglish
Pages (from-to)9168-9172
Number of pages5
JournalJournal of Materials Chemistry B
Volume3
Issue number47
DOIs
Publication statusPublished - 2015
Externally publishedYes

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Peng, L., Gao, M., Cai, X., Zhang, R., Li, K., Feng, G., Tong, A., & Liu, B. (2015). A fluorescent light-up probe based on AIE and ESIPT processes for β-galactosidase activity detection and visualization in living cells. Journal of Materials Chemistry B, 3(47), 9168-9172. https://doi.org/10.1039/c5tb01938a