Cheng L, Fu J, Tsukamoto A, Hawley R G
Research Division, SyStemix, Inc., Palo Alto, CA 94304, USA.
Nat Biotechnol. 1996 May;14(5):606-9. doi: 10.1038/nbt0596-606.
Two mutants of the green fluorescent protein (GFP), RSGFP4 and GFPS65T, have been recently created which differ from the wildtype GFP of A. victoria in their excitation maxima. Here we show that human fibroblasts transfected with either of the two mutant GFP genes emit a green fluorescence that is 18-fold brighter than the cells transfected with the wildtype GFP gene. Retroviral vectors expressing the improved GFP gene were also constructed to determine their suitability for stable gene transduction into mammalian cells. The inclusion of the RSGFP4 gene in a retroviral vector did not reduce the viral titer and resulted in a fluorescent signal in viable transduced cells detectable by both fluorescence microscopy and fluorescence-activated cell sorter (FACS) analysis. Therefore, the improved mutant GFP provides a vital marker for monitoring gene transfer and expression in mammalian cells.
最近已构建出绿色荧光蛋白(GFP)的两种突变体,即RSGFP4和GFPS65T,它们激发峰的波长与维多利亚多管水母的野生型GFP不同。在此我们表明,用这两种突变GFP基因中的任何一种转染的人成纤维细胞发出的绿色荧光,比用野生型GFP基因转染的细胞亮18倍。还构建了表达改良GFP基因的逆转录病毒载体,以确定它们用于将基因稳定转导到哺乳动物细胞中的适用性。将RSGFP4基因整合到逆转录病毒载体中不会降低病毒滴度,并在通过荧光显微镜和荧光激活细胞分选仪(FACS)分析均可检测到的存活转导细胞中产生荧光信号。因此,改良的突变GFP为监测哺乳动物细胞中的基因转移和表达提供了一个重要标记。