An improved cyan fluorescent protein variant useful for FRET

被引:840
作者
Rizzo, MA [1 ]
Springer, GH [1 ]
Granada, B [1 ]
Piston, DW [1 ]
机构
[1] Vanderbilt Univ, Med Ctr, Dept Physiol & Mol Biophys, Nashville, TN 37232 USA
关键词
D O I
10.1038/nbt945
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Many genetically encoded biosensors use Forster resonance energy transfer (FRET) between fluorescent proteins to report biochemical phenomena in living cells. Most commonly, the enhanced cyan fluorescent protein (ECFP) is used as the donor fluorophore, coupled with one of several yellow fluorescent protein (YFP) variants as the acceptor. ECFP is used despite several spectroscopic disadvantages, namely a low quantum yield, a low extinction coefficient and a fluorescence lifetime that is best fit by a double exponential. To improve the characteristics of ECFP for FRET measurements, we used a site-directed mutagenesis approach to overcome these disadvantages. The resulting variant, which we named Cerulean (ECFP/S72A/Y145A/H148D), has a greatly improved quantum yield, a higher extinction coefficient and a fluorescence lifetime that is best fit by a single exponential. Cerulean is 2.5-fold brighter than ECFP and replacement of ECFP with Cerulean substantially improves the signal-to-noise ratio of a FRET-based sensor for glucokinase activation.
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收藏
页码:445 / 449
页数:5
相关论文
共 20 条
[1]   Expansion of the genetic code enables design of a novel "gold'' class of green fluorescent proteins [J].
Bae, JH ;
Rubini, M ;
Jung, G ;
Wiegand, G ;
Seifert, MHJ ;
Azim, MK ;
Kim, JS ;
Zumbusch, A ;
Holak, TA ;
Moroder, L ;
Huber, R ;
Budisa, N .
JOURNAL OF MOLECULAR BIOLOGY, 2003, 328 (05) :1071-1081
[2]   Fluorescence lifetime imaging microscopy: spatial resolution of biochemical processes in the cell [J].
Bastiaens, PIH ;
Squire, A .
TRENDS IN CELL BIOLOGY, 1999, 9 (02) :48-52
[3]  
Cubitt AB, 1999, METHOD CELL BIOL, V58, P19
[4]   Reducing the environmental sensitivity of yellow fluorescent protein - Mechanism and applications [J].
Griesbeck, O ;
Baird, GS ;
Campbell, RE ;
Zacharias, DA ;
Tsien, RY .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (31) :29188-29194
[5]   Engineering green fluorescent protein for improved brightness, longer wavelengths and fluorescence resonance energy transfer [J].
Hein, R ;
Tsien, RY .
CURRENT BIOLOGY, 1996, 6 (02) :178-182
[6]   Fluorescent indicators for Ca2+ based on green fluorescent proteins and calmodulin [J].
Miyawaki, A ;
Llopis, J ;
Heim, R ;
McCaffery, JM ;
Adams, JA ;
Ikura, M ;
Tsien, RY .
NATURE, 1997, 388 (6645) :882-887
[7]   A variant of yellow fluorescent protein with fast and efficient maturation for cell-biological applications [J].
Nagai, T ;
Ibata, K ;
Park, ES ;
Kubota, M ;
Mikoshiba, K ;
Miyawaki, A .
NATURE BIOTECHNOLOGY, 2002, 20 (01) :87-90
[8]  
Ormo M, 1996, SCIENCE, V273, P1392, DOI 10.1126/science.273.5280.1392
[9]  
Patterson G, 2001, J CELL SCI, V114, P837
[10]   Forster distances between green fluorescent protein pairs [J].
Patterson, GH ;
Piston, DW ;
Barisas, BG .
ANALYTICAL BIOCHEMISTRY, 2000, 284 (02) :438-440