Murakami Hiroshi, Kourouklis Dimitrios, Suga Hiroaki
Department of Chemistry, University at Buffalo, The State University of New York, Buffalo, NY 14260, USA.
Chem Biol. 2003 Nov;10(11):1077-84. doi: 10.1016/j.chembiol.2003.10.010.
Here, we report a simple and economical tRNA aminoacylation system based upon a resin-immobilized ribozyme, referred to as Flexiresin. This catalytic system features a broad spectrum of activities toward various phenylalanine (Phe) analogs and suppressor tRNAs. Most importantly, it allows users to perform the tRNA aminoacylation reaction and isolate the aminoacylated tRNAs in a few hours. We coupled the Flexiresin system with a high-performance cell-free translation system and demonstrated protein mutagenesis with seven different Phe analogs in parallel. Thus, the technology developed herein provides a new tool that significantly simplifies the procedures for the synthesis of aminoacyl-tRNAs charged with nonnatural amino acids, which makes the nonnatural amino acid mutagenesis of proteins more user accessible.
在此,我们报道了一种基于树脂固定化核酶(称为Flexiresin)的简单且经济的tRNA氨酰化系统。该催化系统对各种苯丙氨酸(Phe)类似物和抑制性tRNA具有广泛的活性。最重要的是,它允许用户在几个小时内进行tRNA氨酰化反应并分离氨酰化的tRNA。我们将Flexiresin系统与高性能无细胞翻译系统相结合,并同时用七种不同的Phe类似物进行了蛋白质诱变。因此,本文开发的技术提供了一种新工具,该工具显著简化了合成携带非天然氨基酸的氨酰-tRNA的程序,这使得蛋白质的非天然氨基酸诱变对用户来说更容易操作。