Fischer Markus, Haase Ilka, Wiesner Sebastian, Müller-Taubenberger Annette
Lehrstuhl für Organische Chemie und Biochemie, Technische Universität München, Lichtenbergstr. 4, D-85747 Garching, Germany.
FEBS Lett. 2006 May 1;580(10):2495-502. doi: 10.1016/j.febslet.2006.03.082. Epub 2006 Apr 17.
Fluorescent proteins are versatile tools for live cell imaging studies. In particular, recent progress was achieved in the development of monomeric red fluorescent proteins (mRFPs) that show improved properties in respect to maturation and intracellular fluorescence. mRFPmars, a red fluorescent protein designed especially for the use in Dictyostelium, proved to be a brilliant label for different cytoskeletal elements. Here we report on the synthesis of a humanized version of a monomeric RFP, mRFPruby, which differs in sequence from mRFPmars in four amino acids and has a codon usage that is optimized for the application in mammalian cells. In order to demonstrate the usefulness of this new mRFP variant, mRFPruby fused to beta-actin was expressed in different mouse cell lines and used to visualize actin cytoskeleton dynamics by live cell microscopy.
荧光蛋白是活细胞成像研究中用途广泛的工具。特别是,单体红色荧光蛋白(mRFPs)的开发取得了最新进展,其在成熟度和细胞内荧光方面表现出改进的特性。mRFPmars是一种专门设计用于盘基网柄菌的红色荧光蛋白,已证明是用于标记不同细胞骨架成分的出色标记物。在此,我们报告了一种单体RFP人源化版本mRFPruby的合成,它在四个氨基酸的序列上与mRFPmars不同,并且具有针对在哺乳动物细胞中应用而优化的密码子使用情况。为了证明这种新的mRFP变体的实用性,将与β-肌动蛋白融合的mRFPruby在不同的小鼠细胞系中表达,并通过活细胞显微镜用于可视化肌动蛋白细胞骨架动力学。