Shaner Nathan C, Patterson George H, Davidson Michael W
The Salk Institute for Biological Studies, 10010 North Torrey Pines Road, La Jolla, CA 92037, USA.
J Cell Sci. 2007 Dec 15;120(Pt 24):4247-60. doi: 10.1242/jcs.005801.
Current fluorescent protein (FP) development strategies are focused on fine-tuning the photophysical properties of blue to yellow variants derived from the Aequorea victoria jellyfish green fluorescent protein (GFP) and on the development of monomeric FPs from other organisms that emit in the yellow-orange to far-red regions of the visible light spectrum. Progress toward these goals has been substantial, and near-infrared emitting FPs may loom over the horizon. The latest efforts in jellyfish variants have resulted in new and improved monomeric BFP, CFP, GFP and YFP variants, and the relentless search for a bright, monomeric and fast-maturing red FP has yielded a host of excellent candidates, although none is yet optimal for all applications. Meanwhile, photoactivatable FPs are emerging as a powerful class of probes for intracellular dynamics and, unexpectedly, as useful tools for the development of superresolution microscopy applications.
当前荧光蛋白(FP)的开发策略主要集中在对源自维多利亚多管水母绿色荧光蛋白(GFP)的蓝色至黄色变体的光物理特性进行微调,以及开发来自其他生物体的单体荧光蛋白,这些荧光蛋白在可见光光谱的黄橙色至远红色区域发光。在实现这些目标方面已经取得了重大进展,近红外发射荧光蛋白可能即将出现。对水母变体的最新研究成果产生了新的、改良的单体蓝色荧光蛋白(BFP)、青色荧光蛋白(CFP)、绿色荧光蛋白(GFP)和黄色荧光蛋白(YFP)变体,并且对明亮、单体且成熟迅速的红色荧光蛋白的不懈探索已经产生了许多优秀的候选物,尽管尚无一种对所有应用都是最优的。与此同时,光激活荧光蛋白正在成为一类用于细胞内动力学研究的强大探针,并且出乎意料地,也成为了用于超分辨率显微镜应用开发的有用工具。