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Highly Stable Red-Emissive Ratiometric Probe for Monitoring β-Galactosidase Activity Using Fluorescence Microscopy and Flow Cytometry
  • Lee, Hyo Won ;
  • Juvekar, Vinayak ;
  • Lee, Dong Joon ;
  • Kim, Sun Mi ;
  • Kim, Hwan Myung
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Publication Year
2021-11-09
Publisher
American Chemical Society
Citation
Analytical Chemistry, Vol.93, pp.14778-14783
Mesh Keyword
Enzymes activityFluorescent probesHighly stablesLive cellLive tissueOvarian cancersRatiometricRed emissiveReporter enzymesβ- Galactosidase
All Science Classification Codes (ASJC)
Analytical Chemistry
Abstract
β-Galactosidase (β-gal), well known as a useful reporter enzyme, is a potent biomarker for various diseases such as colorectal and ovarian cancers. We have developed a highly stable red-emissive ratiometric fluorescent probe (CCGal) for quantitatively monitoring the β-gal enzyme activity in live cells and tissues. This ratiometric probe showed a fast emission color change (620-662 nm) in response to β-gal selectively, which was accompanied by high enzyme reaction efficacy, cell-staining ability, and outstanding stability with minimized cytotoxicity. Confocal fluorescence microscopy ratiometric images, combined with fluorescence-activated cell sorting flow cytometry, demonstrated that CCGal1 could provide useful information for the diagnosis, prognosis, and treatment of β-gal enzyme activity-related diseases such as colorectal and ovarian cancers. Further, it may yield meaningful strategies for designing and modifying multifunctional bioprobes with different biomedical applications.
Language
eng
URI
https://dspace.ajou.ac.kr/dev/handle/2018.oak/32362
DOI
https://doi.org/10.1021/acs.analchem.1c03453
Fulltext

Type
Article
Funding
This study was supported by grants from the National Leading Research Lab Program of the National Research Foundation of Korea (NRF), funded by the Korean Government (MSIP) (NRF-2019R1A2B5B03100278), Center for Convergence Research of Neurological Disorders (NRF-2019R1A5A2026045), Basic Science Research Program (NRF-2021R1A6A1A10044950), and Ajou University research fund. We acknowledge Yusik Lim and Minkyung Kim at LK Bioscience in Korea for their assistance in flow cytometry analysis.
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Kim, Hwan Myung김환명
Department of Chemistry
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