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ACS Chem Biol ; 16(11): 2109-2115, 2021 11 19.
Article in English | MEDLINE | ID: mdl-34652894

ABSTRACT

Bilin-binding fluorescent proteins like UnaG-bilirubin are noncovalent ligand-dependent reporters for oxygen-free microscopy but are restricted to blue and far-red fluorescence. Here we describe a high-throughput screening approach to provide a new UnaG-ligand pair that can be excited in the 532 nm green excitation microscopy channel. We identified a novel orange UnaG-ligand pair that maximally emits at 581 nm. Whereas the benzothiazole-based ligand itself is nominally fluorescent, the compound binds UnaG with high affinity (Kd = 3 nM) to induce a 2.5-fold fluorescence intensity enhancement and a 10 nm red shift. We demonstrated this pair in the anaerobic fluorescence microscopy of the prevalent gut bacterium Bacteroides thetaiotaomicron and in Escherichia coli. This UnaG-ligand pair can also be coupled to IFP2.0-biliverdin to differentiate cells in mixed-species two-color imaging. Our results demonstrate the versatility of the UnaG ligand-binding pocket and extend the ability to image cells at longer wavelengths in anoxic environments.


Subject(s)
Bacteroides thetaiotaomicron/cytology , Benzothiazoles/chemistry , Escherichia coli/cytology , Fluorescent Dyes/chemistry , Green Fluorescent Proteins/chemistry , Benzothiazoles/metabolism , Fluorescent Dyes/metabolism , Green Fluorescent Proteins/metabolism , High-Throughput Screening Assays , Ligands , Microscopy, Fluorescence , Protein Binding
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