TY - JOUR
T1 - Improved fluorescence and dual color detection with enhanced blue and green variants of the green fluorescent protein
AU - Yang, Te Tuan
AU - Sinai, Parisa
AU - Green, Gisele
AU - Kitts, Paul A.
AU - Chen, Yih Tai
AU - Lybarger, Lonnie
AU - Chervenak, Robert
AU - Patterson, George H.
AU - Piston, David W.
AU - Kain, Steven R.
PY - 1998/4/3
Y1 - 1998/4/3
N2 - The green fluorescent protein (GFP) from the jellyfish Aequorea victoria 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°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.
AB - The green fluorescent protein (GFP) from the jellyfish Aequorea victoria 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°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.
UR - http://www.scopus.com/inward/record.url?scp=0032478788&partnerID=8YFLogxK
U2 - 10.1074/jbc.273.14.8212
DO - 10.1074/jbc.273.14.8212
M3 - Article
C2 - 9525926
AN - SCOPUS:0032478788
SN - 0021-9258
VL - 273
SP - 8212
EP - 8216
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 14
ER -