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用于高等植物的绿色荧光蛋白(GFP)的可溶性、高荧光变体。

Soluble, highly fluorescent variants of green fluorescent protein (GFP) for use in higher plants.

作者信息

Davis S J, Vierstra R D

机构信息

Department of Horticulture, University of Wisconsin-Madison 53706, USA.

出版信息

Plant Mol Biol. 1998 Mar;36(4):521-8. doi: 10.1023/a:1005991617182.

Abstract

Green fluorescent protein (GFP) from Aequorea victoria has rapidly become a standard reporter in many biological systems. However, the use of GFP in higher plants has been limited by aberrant splicing of the corresponding mRNA and by protein insolubility. It has been shown that GFP can be expressed in Arabidopsis thaliana after altering the codon usage in the region that is incorrectly spliced, but the fluorescence signal is weak, possibly due to aggregation of the encoded protein. Through site-directed mutagenesis, we have generated a more soluble version of the codon-modified GFP called soluble-modified GFP (smGFP). The excitation and emission spectra for this protein are nearly identical to wild-type GFP. When introduced into A. thaliana, greater fluorescence was observed compared to the codon-modified GFP, implying that smGFP is 'brighter' because more of it is present in a soluble and functional form. Using the smGFP template, two spectral variants were created, a soluble-modified red-shifted GFP (smRS-GFP) and a soluble-modified blue-fluorescent protein (smBFP). The increased fluorescence output of smGFP will further the use of this reporter in higher plants. In addition, the distinct spectral characters of smRS-GFP and smBFP should allow for dual monitoring of gene expression, protein localization, and detection of in vivo protein-protein interactions.

摘要

维多利亚多管水母的绿色荧光蛋白(GFP)已迅速成为许多生物系统中的标准报告基因。然而,GFP在高等植物中的应用受到相应mRNA异常剪接和蛋白质不溶性的限制。研究表明,在改变错误剪接区域的密码子使用后,GFP可以在拟南芥中表达,但荧光信号较弱,这可能是由于编码蛋白的聚集所致。通过定点诱变,我们生成了一种更易溶的密码子修饰GFP版本,称为可溶性修饰GFP(smGFP)。该蛋白的激发光谱和发射光谱与野生型GFP几乎相同。当将其导入拟南芥时,与密码子修饰的GFP相比,观察到了更强的荧光,这意味着smGFP“更亮”,因为它更多地以可溶且有功能的形式存在。利用smGFP模板,创建了两个光谱变体,一个是可溶性修饰的红移GFP(smRS-GFP),另一个是可溶性修饰的蓝色荧光蛋白(smBFP)。smGFP荧光输出的增加将进一步推动该报告基因在高等植物中的应用。此外,smRS-GFP和smBFP独特的光谱特性应能实现对基因表达、蛋白质定位以及体内蛋白质-蛋白质相互作用检测的双重监测。

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