Sörensen Meike, Lippuner Christoph, Kaiser Toralf, Misslitz Ana, Aebischer Toni, Bumann Dirk
Department of Molecular Biology, Max-Planck-Institute for Infection Biology, Schumannstr. 21/22, D-10117 Berlin, Germany.
FEBS Lett. 2003 Sep 25;552(2-3):110-4. doi: 10.1016/s0014-5793(03)00856-1.
A rapidly maturing variant of the red fluorescent protein DsRed was optimized for bacterial expression by random mutagenesis. The brightest variant contains six mutations, two of which (S4T and a silent mutation in codon 2) explain most of the fluorescence enhancement. The novel variants are expressed at 9-60-fold higher levels in Escherichia coli compared to DsRed.T3, but are not superior fluorophores on a per molecule basis. In contrast to previously available DsRed variants, DsRed.T3_S4T is sufficiently bright to monitor Salmonella gene expression in infected animals using flow cytometry. However, no fluorescence enhancement was observed in Leishmania or HeLa cells, indicating that these novel variants are specifically useful for bacteria.
通过随机诱变优化了红色荧光蛋白DsRed的一种快速成熟变体,用于细菌表达。最亮的变体包含六个突变,其中两个(S4T和密码子2中的一个沉默突变)解释了大部分荧光增强现象。与DsRed.T3相比,这些新变体在大肠杆菌中的表达水平高9至60倍,但在单个分子基础上并非更优异的荧光团。与先前可用的DsRed变体不同,DsRed.T3_S4T足够亮,可使用流式细胞术监测感染动物中沙门氏菌的基因表达。然而,在利什曼原虫或HeLa细胞中未观察到荧光增强,表明这些新变体对细菌具有特异性用途。