| Literature DB >> 27400827 |
Tomohiro Doura1, Mako Kamiya2,3, Fumiaki Obata4, Yoshifumi Yamaguchi4,5, Takeshi Y Hiyama6,7, Takashi Matsuda7, Akiyoshi Fukamizu8,9, Masaharu Noda6,7, Masayuki Miura4,10, Yasuteru Urano11,12,13.
Abstract
The LacZ gene, which encodes Escherichia coli β-galactosidase, is widely used as a marker for cells with targeted gene expression or disruption. However, it has been difficult to detect lacZ-positive cells in living organisms or tissues at single-cell resolution, limiting the utility of existing lacZ reporters. Herein we present a newly developed fluorogenic β-galactosidase substrate suitable for labeling live cells in culture, as well as in living tissues. This precisely functionalized fluorescent probe exhibited dramatic activation of fluorescence upon reaction with the enzyme, remained inside cells by anchoring itself to intracellular proteins, and provided single-cell resolution. Neurons labeled with this probe preserved spontaneous firing, which was enhanced by application of ligands of receptors expressed in the cells, suggesting that this probe would be applicable to investigate functions of targeted cells in living tissues and organisms.Entities:
Keywords: fluorescent probes; lacZ; quinone methide intermediates; single-cell resolution; β-galactosidase
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Year: 2016 PMID: 27400827 DOI: 10.1002/anie.201603328
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336