Division of Molecular Biosciences, Imperial College London, London, SW7 2AZ, United Kingdom.
Proteins. 2015 Mar;83(3):397-402. doi: 10.1002/prot.24742. Epub 2015 Jan 13.
The fluorescent protein Dronpa undergoes reversible photoswitching reactions between the bright "on" and dark "off" states via photoisomerization and proton transfer reactions. We report the room temperature crystal structure of the fast switching Met159Thr mutant of Dronpa at 2.0-Å resolution in the bright on state. Structural differences with the wild type include shifted backbone positions of strand β8 containing Thr159 as well as an altered A-C dimer interface involving strands β7, β8, β10, and β11. The Met159Thr mutation increases the cavity volume for the p-hydroxybenzylidene-imidazolinone chromophore as a result of both the side chain difference and the backbone positional differences.
荧光蛋白 Dronpa 通过光异构化和质子转移反应在明亮的“开”和黑暗的“关”状态之间经历可逆的光开关反应。我们报告了 Dronpa 的快速切换 Met159Thr 突变体在明亮的“开”状态下在 2.0-Å 分辨率的室温晶体结构。与野生型相比,结构差异包括含有 Thr159 的β8 链的骨架位置移动以及涉及β7、β8、β10 和β11 链的 A-C 二聚体界面的改变。Met159Thr 突变增加了 p-羟基苯亚甲基-咪唑啉酮生色团的腔体积,这是由于侧链差异和骨架位置差异的共同作用。