De Novo Generation of Mutually Orthogonal Aminoacyl-tRNA Synthetase/tRNA Pairs

被引:70
作者
Neumann, Heinz [1 ]
Slusarczyk, Adrian L. [1 ]
Chin, Jason W. [1 ]
机构
[1] MRC, Mol Biol Lab, Cambridge CB2 0QH, England
基金
英国医学研究理事会; 欧洲研究理事会;
关键词
GENETIC-CODE EXPANSION; RECOMBINANT PROTEINS;
D O I
10.1021/ja9068722
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The genetic code sets the correspondence between codons and the amino acids they encode in protein translation. The code is enforced by aminoacyl-tRNA synthetase/tRNA pairs, which direct the unique coupling of specific amino acids with specific anticodons. The evolutionary record suggests that a primitive genetic code expanded into the current genetic code, over billions of years, through duplication and specialization (neofunctionalization) of aminoacyl-tRNA synthetases and tRNAs from common ancestral synthetase/tRNA pairs. This process produced the current set of mutually orthogonal aminoacyl-tRNA synthetases and tRNAs that direct natural protein synthesis. Here we demonstrate the creation of new orthogonal pairs, which are mutually orthogonal with existing orthogonal pairs, de novo, by a logical series of steps implemented in the laboratory, via the de novo generation of orthogonality in RNA-RNA interactions, protein-RNA interactions, and small molecule substrate selection by protein catalysts. Our laboratory evolution experiments provide experimental evidence for duplication and specialization as a plausible route to the current set of synthetases and tRNAs via natural evolution. Moreover our experiments extend billions of years of natural evolution and demonstrate that the small number of naturally occurring orthogonal aminoacyl-tRNA synthetase/tRNA pairs do not place an intrinsic limitation on the scope of synthetic genetic code expansion for the incorporation of multiple distinct unnatural amino acids into proteins or the synthesis and evolution of unnatural polymers in cells.
引用
收藏
页码:2142 / +
页数:5
相关论文
共 16 条
[1]   Addition of a photocrosslinking amino acid to the genetic code of Escherichia coli [J].
Chin, JW ;
Martin, AB ;
King, DS ;
Wang, L ;
Schultz, PG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (17) :11020-11024
[2]   GENERAL NATURE OF GENETIC CODE FOR PROTEINS [J].
CRICK, FH ;
BRENNER, S ;
WATSTOBI.RJ ;
BARNETT, L .
NATURE, 1961, 192 (480) :1227-&
[3]   Aminoacyl-tRNA synthetases: potential markers of genetic code development [J].
de Pouplana, LR ;
Schimmel, P .
TRENDS IN BIOCHEMICAL SCIENCES, 2001, 26 (10) :591-596
[4]   Major tyrosine identity determinants in Methanococcus jannaschii and Saccharomyces cerevisiae tRNATyr conserved but expressed differently [J].
Fechter, P ;
Rudinger-Thirion, J ;
Tukalo, M ;
Giegé, R .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2001, 268 (03) :761-767
[5]   Structural basis for orthogonal tRNA specificities of tyrosyl-tRNA synthetases for genetic code expansion [J].
Kobayashi, T ;
Nureki, O ;
Ishitani, R ;
Yaremchuk, A ;
Tukalo, M ;
Cusack, S ;
Sakamoto, K ;
Yokoyama, S .
NATURE STRUCTURAL BIOLOGY, 2003, 10 (06) :425-432
[6]   Engineering a tRNA and aminoacyl-tRNA synthetase for the site-specific incorporation of unnatural amino acids into proteins in vivo [J].
Liu, DR ;
Magliery, TJ ;
Pasternak, M ;
Schultz, PG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (19) :10092-10097
[7]  
NEUMANN H, 2010, NATURE IN PRESS, P4
[8]   Genetically encoding Nε-acetyllysine in recombinant proteins [J].
Neumann, Heinz ;
Peak-Chew, Sew Y. ;
Chin, Jason W. .
NATURE CHEMICAL BIOLOGY, 2008, 4 (04) :232-234
[9]   Genetic Encoding and Labeling of Aliphatic Azides and Alkynes in Recombinant Proteins via a Pyrrolysyl-tRNA Synthetase/tRNACUA Pair and Click Chemistry [J].
Nguyen, Duy P. ;
Lusic, Hrvoje ;
Neumann, Heinz ;
Kapadnis, Prashant B. ;
Deiters, Alexander ;
Chin, Jason W. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (25) :8720-+
[10]   A network of orthogonal ribosome•mRNA pairs [J].
Rackham, O ;
Chin, JW .
NATURE CHEMICAL BIOLOGY, 2005, 1 (03) :159-166