Improved fluorescence and dual color detection with enhanced blue and green variants of the green fluorescent protein

被引:111
作者
Yang, TT
Sinai, P
Green, G
Kitts, PA
Chen, YT
Lybarger, L
Chervenak, R
Patterson, GH
Piston, DW
Kain, SR
机构
[1] Clontech Labs Inc, Cell Biol Grp, Palo Alto, CA 94303 USA
[2] Stanford Univ, Dept Cellular & Mol Physiol, Sch Med, Stanford, CA 94305 USA
[3] Louisiana State Univ, Med Ctr, Dept Microbiol & Immunol, Shreveport, LA 71130 USA
[4] Vanderbilt Univ, Dept Mol Physiol & Biophys, Sch Med, Nashville, TN 37232 USA
关键词
D O I
10.1074/jbc.273.14.8212
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The green fluorescent protein (GFP) from the jellyfish Aequorea victor ia is a versatile reporter protein for monitoring gene expression and protein localization in a variety of systems, Applications using GFP reporters have expanded greatly due to the availability of mutants with altered spectral properties, including several blue emission variants, all of which contain the single point mutation Tyr-66 to His in the chromophore region of the protein. However, previously described "BFP" reporters have limited utility, primarily due to relatively dim fluorescence and low expression levels attained in higher eukaryotes with such variants. To improve upon these qualities, we have combined a blue emission mutant of GFP containing four point mutations (Phe-64 to Leu, Ser-65 to Thr, Tyr-66 to His, and Tyr-145 to Phe) with a synthetic gene sequence containing codons preferentially found in highly expressed human proteins. These mutations were chosen to optimize expression of properly folded fluorescent protein in mammalian cells cultured at 37 degrees C and to maximize signal intensity. The combination of improved fluorescence and higher expression levels yield an enhanced blue fluorescent protein that provides greater sensitivity and is suitable for dual color detection with green-emitting fluorophores.
引用
收藏
页码:8212 / 8216
页数:5
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