RED-SHIFTED EXCITATION MUTANTS OF THE GREEN FLUORESCENT PROTEIN
被引:245
作者:
DELAGRAVE, S
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机构:PALO ALTO INST MOLEC MED,MT VIEW,CA 94043
DELAGRAVE, S
HAWTIN, RE
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机构:PALO ALTO INST MOLEC MED,MT VIEW,CA 94043
HAWTIN, RE
SILVA, CM
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机构:PALO ALTO INST MOLEC MED,MT VIEW,CA 94043
SILVA, CM
YANG, MM
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机构:PALO ALTO INST MOLEC MED,MT VIEW,CA 94043
YANG, MM
YOUVAN, DC
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机构:PALO ALTO INST MOLEC MED,MT VIEW,CA 94043
YOUVAN, DC
机构:
[1] PALO ALTO INST MOLEC MED,MT VIEW,CA 94043
[2] KAIROS SCI INC,SAN JOSE,CA 95136
来源:
BIO-TECHNOLOGY
|
1995年
/
13卷
/
02期
关键词:
D O I:
10.1038/nbt0295-151
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:
Using optimized combinatorial mutagenesis techniques and Digital Imaging Spectroscopy (DIS), we have isolated mutants of the cloned Aequorea victoria green fluorescent protein (GFP) that show red-shifted excitation spectra similar to that of Renilla reniformis GFP. Selective excitation of wild-type versus Red-Shifted GFP (RSGFP) enables spectral separation of these proteins. Six contiguous codons spanning the tyrosine chromophore region were randomized and sequence analysis of the mutants revealed a tyrosine-glycine consensus. These mutants will enable the simultaneous analysis of two promoters or proteins per cell or organism. In consideration of the multitude of applications which are developing for GFP alone, we envisage that spectrally shifted fluorescent proteins will be of value to a diversity of research programs, including developmental and cell biology, drug-screening, and diagnostic assays.