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增强型绿色荧光蛋白可实现对哺乳动物细胞中基因转移的灵敏检测。

An enhanced green fluorescent protein allows sensitive detection of gene transfer in mammalian cells.

作者信息

Zhang G, Gurtu V, Kain S R

机构信息

Clontech Laboratories, Inc., Palo Alto, California 94303, USA.

出版信息

Biochem Biophys Res Commun. 1996 Oct 23;227(3):707-11. doi: 10.1006/bbrc.1996.1573.

Abstract

The green fluorescent protein (GFP) from the jellyfish Aequorea victoria has become an important marker of gene expression. However, the sensitivity of wild-type GFP has been below that of standard reporter proteins, such as beta-galactosidase, which utilize enzymatic amplification. To improve the detection of GFP in transfected mammalian cells, we have constructed a unique GFP variant which contains chromophore mutations that make the protein 35 times brighter than wild-type GFP, and is codon-optimized for higher expression in mammalian cells. These changes in the GFP coding sequence provide an enhanced GFP (EGFP) that greatly increases the sensitivity of the reporter protein. We show that the EGFP expression vector delivered into mammalian cells gives rise to bright fluorescence that is readily detectable following a 16-24 hr transfection interval. Visual detection of transfected cells with EGFP appears to be more sensitive than equivalent measurements with beta-galactosidase catalyzed conversion of the X-gal substrate. We conclude that EGFP allows sensitive and convenient detection of gene transfer in mammalian cells.

摘要

来自维多利亚多管水母的绿色荧光蛋白(GFP)已成为基因表达的重要标记物。然而,野生型GFP的灵敏度低于标准报告蛋白,如利用酶促放大作用的β-半乳糖苷酶。为了提高在转染的哺乳动物细胞中对GFP的检测,我们构建了一种独特的GFP变体,它含有发色团突变,使该蛋白比野生型GFP亮35倍,并且经过密码子优化以在哺乳动物细胞中实现更高表达。GFP编码序列中的这些变化产生了一种增强型GFP(EGFP),极大地提高了报告蛋白的灵敏度。我们表明,导入哺乳动物细胞的EGFP表达载体可产生明亮的荧光,在转染间隔16 - 24小时后即可轻松检测到。用EGFP对转染细胞进行视觉检测似乎比用β-半乳糖苷酶催化X-gal底物转化进行的等效测量更灵敏。我们得出结论,EGFP能够灵敏且方便地检测哺乳动物细胞中的基因转移。

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