Engineered metal binding sites on green fluorescence protein

被引:74
作者
Richmond, TA
Takahashi, TT
Shimkhada, R
Bernsdorf, J
机构
[1] Pitzer, Claremont McKenna, Joint Sci Dept, Claremont, CA 91711 USA
[2] Scripps Coll, Claremont, CA 91711 USA
关键词
green fluorescent protein; metal binding; fluorescence quenching; mutagenesis;
D O I
10.1006/bbrc.1999.1244
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 ability to assay a variety of metals by noninvasive methods has applications in both biomedical and environmental research. Green fluorescent protein (GFP) is a protein isolated from coelenterates that exhibits spontaneous fluorescence. GFP does not require any exogenous cofactors for fluorescence, and can be easily appended to other proteins at the DNA level, producing a fluorescence-labeled target protein in vivo. Metals in close proximity to chromophores are known to quench fluorescence in a distance-dependent fashion. Potential metal binding sites on the surface of GFP have been identified and mutant proteins have been designed, created, and characterized. These metal-binding mutants of GFP exhibit fluorescence quenching at lower transition metal ion concentrations than those of the wild-type protein. These GFP mutants represent a new class of protein-based metal sensors. (C) 2000 Academic Press.
引用
收藏
页码:462 / 465
页数:4
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