tRNA engineering strategies for genetic code expansion

被引:11
作者
Kim, Youjin [1 ]
Cho, Suho [1 ]
Kim, Joo-Chan [1 ]
Park, Hee-Sung [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Chem, Daejeon, South Korea
基金
新加坡国家研究基金会;
关键词
tRNA engineering; genetic code expansion; directed evolution; rational design; unnatural amino acid; UNNATURAL AMINO-ACIDS; SITE-SPECIFIC INCORPORATION; SUPPRESSOR TRANSFER-RNAS; ESCHERICHIA-COLI; IN-VIVO; NONNATURAL RESIDUES; DIRECTED-EVOLUTION; CRYSTAL-STRUCTURE; AMBER SUPPRESSOR; SYNTHETASE PAIR;
D O I
10.3389/fgene.2024.1373250
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The advancement of genetic code expansion (GCE) technology is attributed to the establishment of specific aminoacyl-tRNA synthetase/tRNA pairs. While earlier improvements mainly focused on aminoacyl-tRNA synthetases, recent studies have highlighted the importance of optimizing tRNA sequences to enhance both unnatural amino acid incorporation efficiency and orthogonality. Given the crucial role of tRNAs in the translation process and their substantial impact on overall GCE efficiency, ongoing efforts are dedicated to the development of tRNA engineering techniques. This review explores diverse tRNA engineering approaches and provides illustrative examples in the context of GCE, offering insights into the user-friendly implementation of GCE technology.
引用
收藏
页数:13
相关论文
共 82 条
[1]   Rewiring Translation for Elongation Factor Tu-Dependent Selenocysteine Incorporation [J].
Aldag, Caroline ;
Broecker, Markus J. ;
Hohn, Michael J. ;
Prat, Laure ;
Hammond, Gifty ;
Plummer, Abigail ;
Soell, Dieter .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2013, 52 (05) :1441-1445
[2]   An expanded genetic code with a functional quadruplet codon [J].
Anderson, JC ;
Wu, N ;
Santoro, SW ;
Lakshman, V ;
King, DS ;
Schultz, PG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (20) :7566-7571
[3]   Adaptation of an orthogonal archaeal leucyl-tRNA and synthetase pair for four-base, amber, and opal suppression [J].
Anderson, JC ;
Schultz, PG .
BIOCHEMISTRY, 2003, 42 (32) :9598-9608
[4]   SITE-SPECIFIC INCORPORATION OF NONNATURAL RESIDUES DURING INVITRO PROTEIN-BIOSYNTHESIS WITH SEMISYNTHETIC AMINOACYL-TRANSFER RNAS [J].
BAIN, JD ;
DIALA, ES ;
GLABE, CG ;
WACKER, DA ;
LYTTLE, MH ;
DIX, TA ;
CHAMBERLIN, AR .
BIOCHEMISTRY, 1991, 30 (22) :5411-5421
[5]   BIOSYNTHETIC SITE-SPECIFIC INCORPORATION OF A NON-NATURAL AMINO-ACID INTO A POLYPEPTIDE [J].
BAIN, JD ;
GLABE, CG ;
DIX, TA ;
CHAMBERLIN, AR ;
DIALA, ES .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1989, 111 (20) :8013-8014
[6]   PREPARATION OF CHEMICALLY MISACYLATED SEMISYNTHETIC NONSENSE SUPPRESSOR TRANSFER-RNAS EMPLOYED IN BIOSYNTHETIC INCORPORATION OF NONNATURAL RESIDUES INTO PROTEINS [J].
BAIN, JD ;
WACKER, DA ;
KUO, EE ;
LYTTLE, MH ;
CHAMBERLIN, AR .
JOURNAL OF ORGANIC CHEMISTRY, 1991, 56 (15) :4615-4625
[7]   Transfer RNAs: diversity in form and function [J].
Berg, Matthew D. ;
Brandl, Christopher J. .
RNA BIOLOGY, 2021, 18 (03) :316-339
[8]   NMR EVIDENCE FOR COMMON TERTIARY STRUCTURE BASE-PAIRS IN YEAST AND ESCHERICHIA-COLI TRANSFER-RNA [J].
BOLTON, PH ;
KEARNS, DR .
NATURE, 1975, 255 (5506) :347-349
[9]   A Tryptophanyl-tRNA Synthetase/tRNA Pair for Unnatural Amino Acid Mutagenesis in E.coli [J].
Chatterjee, Abhishek ;
Xiao, Han ;
Yang, Peng-Yu ;
Soundararajan, Gautam ;
Schultz, Peter G. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2013, 52 (19) :5106-5109
[10]   A Versatile Platform for Single- and Multiple-Unnatural Amino Acid Mutagenesis in Escherichia coli [J].
Chatterjee, Abhishek ;
Sun, Sophie B. ;
Furman, Jennifer L. ;
Xiao, Han ;
Schultz, Peter G. .
BIOCHEMISTRY, 2013, 52 (10) :1828-1837