Wall M A, Socolich M, Ranganathan R
Howard Hughes Medical Institute, The University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, Texas 75390-9050, USA.
Nat Struct Biol. 2000 Dec;7(12):1133-8. doi: 10.1038/81992.
Green fluorescent protein (GFP) has rapidly become a standard tool for investigating a variety of cellular activities, and has served as a model system for understanding spectral tuning in chromophoric proteins. Distant homologs of GFP in reef coral and anemone display two new properties of the fluorescent protein family: dramatically red-shifted spectra, and oligomerization to form tetramers. We now report the 1.9 A crystal structure of DsRed, a red fluorescent protein from Discosoma coral. DsRed monomers show similar topology to GFP, but additional chemical modification to the chromophore extends the conjugated pi-system and likely accounts for the red-shifted spectra. Oligomerization of DsRed occurs at two chemically distinct protein interfaces to assemble the tetramer. The DsRed structure reveals the chemical basis for the functional properties of red fluorescent proteins and provides the basis for rational engineering of this subfamily of GFP homologs.
绿色荧光蛋白(GFP)已迅速成为研究各种细胞活动的标准工具,并作为理解发色蛋白光谱调谐的模型系统。珊瑚礁珊瑚和海葵中GFP的远亲同源物展示了荧光蛋白家族的两个新特性:光谱显著红移,以及寡聚形成四聚体。我们现在报告来自盘状珊瑚的红色荧光蛋白DsRed的1.9埃晶体结构。DsRed单体显示出与GFP相似的拓扑结构,但发色团的额外化学修饰扩展了共轭π-体系,这可能是光谱红移的原因。DsRed的寡聚发生在两个化学性质不同的蛋白质界面以组装四聚体。DsRed结构揭示了红色荧光蛋白功能特性的化学基础,并为合理改造GFP同源物的这个亚家族提供了基础。