Murayama Takashi, Kobayashi Takuya
Department of Cellular and Molecular Pharmacology, Juntendo University Graduate School of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo, 113-8421, Japan,
Methods Mol Biol. 2014;1177:151-61. doi: 10.1007/978-1-4939-1034-2_12.
Green fluorescent protein (GFP) is the most widespread fluorescent reporter for cellular localization and interaction of proteins. Because GFP itself is not the protein purification tag, protein purification is generally carried out with the aid of additional affinity tags. We have recently engineered a "multifunctional GFP" (mfGFP), a variant of enhanced GFP (EGFP), in which multiple affinity tags are inserted in tandem into an internal loop of EGFP. The mfGFP can be used as a fluorescent reporter and an affinity tag, and is compatible with various expression systems in prokaryotic and eukaryotic cells. Herein, we describe detailed procedures for the expression and purification of mfGFP fusion proteins in mammalian cells. A method for tandem affinity purification using two different tags within mfGFP is also described.
绿色荧光蛋白(GFP)是用于蛋白质细胞定位和相互作用的最广泛使用的荧光报告蛋白。由于GFP本身不是蛋白质纯化标签,蛋白质纯化通常借助额外的亲和标签来进行。我们最近构建了一种“多功能GFP”(mfGFP),它是增强型GFP(EGFP)的变体,其中多个亲和标签串联插入到EGFP的一个内部环中。mfGFP可用作荧光报告蛋白和亲和标签,并且与原核和真核细胞中的各种表达系统兼容。在此,我们描述了在哺乳动物细胞中表达和纯化mfGFP融合蛋白的详细步骤。还描述了一种在mfGFP内使用两种不同标签进行串联亲和纯化的方法。