| Autor: |
Zhang H; Center for Membrane and Cell Physiology, University of Virginia, Charlottesville, VA 22908, USA.; Department of Chemistry, University of Virginia, Charlottesville, VA 22904, USA., Tian X; Center for Membrane and Cell Physiology, University of Virginia, Charlottesville, VA 22908, USA.; Department of Molecular Physiology and Biological Physics, University of Virginia, Charlottesville, VA 22908, USA., Zhang J; Center for Membrane and Cell Physiology, University of Virginia, Charlottesville, VA 22908, USA.; Department of Molecular Physiology and Biological Physics, University of Virginia, Charlottesville, VA 22908, USA., Ai HW; Center for Membrane and Cell Physiology, University of Virginia, Charlottesville, VA 22908, USA.; Department of Chemistry, University of Virginia, Charlottesville, VA 22904, USA.; Department of Molecular Physiology and Biological Physics, University of Virginia, Charlottesville, VA 22908, USA.; The UVA Comprehensive Cancer Center, University of Virginia, Charlottesville, VA 22908, USA. |
| Abstrakt: |
Introducing 3-aminotyrosine (aY), a noncanonical amino acid (ncAA), into green fluorescent protein (GFP)-like chromophores shows promise for achieving red-shifted fluorescence. However, inconsistent results, including undesired green fluorescent species, hinder the effectiveness of this approach. In this study, we optimized expression conditions for an aY-derived cpGFP (aY-cpGFP). Key factors like rich culture media and oxygen restriction pre- and post-induction enabled high-yield, high-purity production of the red-shifted protein. We also engineered two variants of aY-cpGFP with enhanced brightness by mutating a few amino acid residues surrounding the chromophore. We further investigated the sensitivity of the aY-derived protein to metal ions, reactive oxygen species (ROS), and reactive nitrogen species (RNS). Incorporating aY into cpGFP had minimal impact on metal ion reactivity but increased the response to RNS. Expanding on these findings, we examined aY-cpGFP expression in mammalian cells and found that reductants in the culture media significantly increased the red-emitting product. Our study indicates that optimizing expression conditions to promote a reduced cellular state proved effective in producing the desired red-emitting product in both E. coli and mammalian cells, while targeted mutagenesis-based protein engineering can further enhance brightness and increase method robustness. |
