4.6 Article

New Orange Ligand-Dependent Fluorescent Reporter for Anaerobic Imaging

Journal

ACS CHEMICAL BIOLOGY
Volume 16, Issue 11, Pages 2109-2115

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acschembio.1c00391

Keywords

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Funding

  1. Army Research Office grant [W911NF-18-1-0339]
  2. National Science Foundation [Che1608553, Che1904759]
  3. National Science Foundation Graduate Research Fellowship Program [DGE-1256260]
  4. Center for Chemical Genomics (CCG) at the University of Michigan Life Sciences Institute

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A novel orange UnaG-ligand pair has been identified, which can be excited in the 532 nm green excitation microscopy channel and emits at 581 nm, showing high affinity for UnaG and a significant increase in fluorescence intensity and red shift in anoxic environments. This discovery expands the versatility of UnaG ligand-binding pocket for cell imaging at longer wavelengths.
Bilin-binding fluorescent proteins like UnaG-bilirubin are noncovaleiff 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 (K-d = 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.

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