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Article Abstract

Solvatochromic compounds have emerged as valuable environment-sensitive probes for biological research. Here we used thiol-reactive solvatochromic analogs of the green fluorescent protein (GFP) chromophore to track conformational changes in two proteins, recoverin and the A adenosine receptor (AAR). Two dyes showed Ca-induced fluorescence changes when attached to recoverin. Our best-performing dye, DyeC, exhibited agonist-induced changes in both intensity and shape of its fluorescence spectrum when attached to AAR; none of these effects were observed with other common environment-sensitive dyes. Molecular dynamics simulations showed that activation of the AAR led to a more confined and hydrophilic environment for DyeC. Additionally, an allosteric modulator of AAR induced distinct fluorescence changes in the DyeC spectrum, indicating a unique receptor conformation. Our study demonstrated that GFP-inspired dyes are effective for detecting structural changes in G protein-coupled receptors (GPCRs), offering advantages such as intensity-based and ratiometric tracking, redshifted fluorescence spectra, and sensitivity to allosteric modulation.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11326922PMC
http://dx.doi.org/10.1016/j.isci.2024.110466DOI Listing

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Article Synopsis
  • Solvatochromic compounds are useful probes for biological research, specifically for tracking changes in protein structures.
  • The study utilized thiol-reactive solvatochromic analogs of the GFP chromophore to monitor two proteins: recoverin and the A adenosine receptor (AAR), finding that the best dye (DyeC) showed significant fluorescence changes related to protein activation.
  • The research highlights the potential of GFP-inspired dyes to effectively detect structural changes in G protein-coupled receptors (GPCRs), providing benefits like enhanced sensitivity to conformational changes and the ability to track fluorescence changes in response to different ligands.
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Green fluorescent protein inspired fluorophores.

Adv Colloid Interface Sci

November 2020

State Key Laboratory of Chemical Engineering, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072, PR China.

Green fluorescence proteins (GFP) are appealing to a variety of biomedical and biotechnology applications, such as protein fusion, subcellular localizations, cell visualization, protein-protein interaction, and genetically encoded sensors. To mimic the fluorescence of GFP, various compounds, such as GFP chromophores analogs, hydrogen bond-rich proteins, and aromatic peptidyl nanostructures that preclude free rotation of the aryl-alkene bond, have been developed to adapt them for a fantastic range of applications. Herein, we firstly summarize the structure and luminescent mechanism of GFP.

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Shanghai Key Laboratory of Functional Materials Chemistry & Department of Chemistry, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, PR China.

A green fluorescent protein chromophore inspired chemosenor for Zn(2+) was designed and synthesized. A Zn(2+) specific fluorescence enhancement was observed due to restricted rotation between the 1,10-phenanthroline and imidazolone moieties.

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