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利用固相核酶氨酰化系统对遗传密码进行重新编程。

Using a solid-phase ribozyme aminoacylation system to reprogram the genetic code.

作者信息

Murakami Hiroshi, Kourouklis Dimitrios, Suga Hiroaki

机构信息

Department of Chemistry, University at Buffalo, The State University of New York, Buffalo, NY 14260, USA.

出版信息

Chem Biol. 2003 Nov;10(11):1077-84. doi: 10.1016/j.chembiol.2003.10.010.

Abstract

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.

摘要

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。

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