Literature DB >> 14652075

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

Hiroshi Murakami1, Dimitrios Kourouklis, Hiroaki Suga.   

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.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 14652075     DOI: 10.1016/j.chembiol.2003.10.010

Source DB:  PubMed          Journal:  Chem Biol        ISSN: 1074-5521


  15 in total

1.  The RNA origin of transfer RNA aminoacylation and beyond.

Authors:  Hiroaki Suga; Gosuke Hayashi; Naohiro Terasaka
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2011-10-27       Impact factor: 6.237

2.  In vivo incorporation of multiple unnatural amino acids through nonsense and frameshift suppression.

Authors:  Erik A Rodriguez; Henry A Lester; Dennis A Dougherty
Journal:  Proc Natl Acad Sci U S A       Date:  2006-05-25       Impact factor: 11.205

Review 3.  Incorporation of nonstandard amino acids into proteins: principles and applications.

Authors:  Tianwen Wang; Chen Liang; Hongjv Xu; Yafei An; Sha Xiao; Mengyuan Zheng; Lu Liu; Lei Nie
Journal:  World J Microbiol Biotechnol       Date:  2020-04-08       Impact factor: 3.312

Review 4.  tRNA engineering for manipulating genetic code.

Authors:  Takayuki Katoh; Yoshihiko Iwane; Hiroaki Suga
Journal:  RNA Biol       Date:  2017-09-06       Impact factor: 4.652

5.  Initiating translation with D-amino acids.

Authors:  Yuki Goto; Hiroshi Murakami; Hiroaki Suga
Journal:  RNA       Date:  2008-05-30       Impact factor: 4.942

6.  Improved amber and opal suppressor tRNAs for incorporation of unnatural amino acids in vivo. Part 1: minimizing misacylation.

Authors:  Erik A Rodriguez; Henry A Lester; Dennis A Dougherty
Journal:  RNA       Date:  2007-08-13       Impact factor: 4.942

7.  Improved amber and opal suppressor tRNAs for incorporation of unnatural amino acids in vivo. Part 2: evaluating suppression efficiency.

Authors:  Erik A Rodriguez; Henry A Lester; Dennis A Dougherty
Journal:  RNA       Date:  2007-08-13       Impact factor: 4.942

8.  In vitro assays for the determination of aminoacyl-tRNA synthetase editing activity.

Authors:  Kathryn E Splan; Karin Musier-Forsyth; Michal T Boniecki; Susan A Martinis
Journal:  Methods       Date:  2008-02       Impact factor: 3.608

9.  An mRNA-protein fusion at N-terminus for evolutionary protein engineering.

Authors:  Shingo Ueno; Hidenao Arai; Miho Suzuki; Yuzuru Husimi
Journal:  Int J Biol Sci       Date:  2007-08-29       Impact factor: 6.580

10.  Distinct tRNA recognition strategies used by a homologous family of editing domains prevent mistranslation.

Authors:  Mom Das; Oscar Vargas-Rodriguez; Yuki Goto; Hiroaki Suga; Karin Musier-Forsyth
Journal:  Nucleic Acids Res       Date:  2013-12-25       Impact factor: 16.971

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.