Incorporation of nonnatural amino acids into proteins

被引:199
作者
Hendrickson, TL
de Crécy-Lagard, V
Schimmel, P
机构
[1] Johns Hopkins Univ, Dept Chem, Baltimore, MD 21218 USA
[2] Scripps Res Inst, La Jolla, CA 92037 USA
关键词
aminoacyl-tRNA synthetase; suppression; orthogonal; protein biosynthesis;
D O I
10.1146/annurev.biochem.73.012803.092429
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The genetic code is established by the aminoacylation of transfer RNA, reactions in which each amino acid is linked to its cognate tRNA that, in turn, harbors the nucleotide triplet (anticodon) specific to the amino acid. The accuracy of aminoacylation is essential for building and maintaining the universal tree of life. The ability to manipulate and expand the code holds promise for the development of new methods to create novel proteins and to understand the origins of life. Recent efforts to manipulate the genetic code have fulfilled much of this potential. These efforts have led to incorporation of nonnatural amino acids into proteins for a variety of applications and have demonstrated the plausibility of specific proposals for early evolution of the code.
引用
收藏
页码:147 / 176
页数:30
相关论文
共 181 条
[1]   HIV protease inhibitors: Peptidomimetic drugs and future perspectives [J].
Abdel-Rahman, HM ;
Al-karamany, GS ;
El-Koussi, NA ;
Youssef, AF ;
Kiso, Y .
CURRENT MEDICINAL CHEMISTRY, 2002, 9 (21) :1905-1922
[2]   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
[3]   Exploring the limits of codon and anticodon size [J].
Anderson, JC ;
Magliery, TJ ;
Schultz, PG .
CHEMISTRY & BIOLOGY, 2002, 9 (02) :237-244
[4]   SUPPRESSOR GENE SU3+ OF E COLI A STRUCTURAL GENE FOR TYROSINE TRNA [J].
ANDOH, T ;
OZEKI, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1968, 59 (03) :792-&
[5]  
[Anonymous], FESTSCHRIFT A STOLL
[6]   SITE-SPECIFIC MUTAGENESIS WITH UNNATURAL AMINO-ACIDS [J].
ANTHONYCAHILL, SJ ;
GRIFFITH, MC ;
NOREN, CJ ;
SUICH, DJ ;
SCHULTZ, PG .
TRENDS IN BIOCHEMICAL SCIENCES, 1989, 14 (10) :400-403
[7]   Selection and characterization of Escherichia coli variants capable of growth on an otherwise toxic tryptophan analogue [J].
Bacher, JM ;
Ellington, AD .
JOURNAL OF BACTERIOLOGY, 2001, 183 (18) :5414-5425
[8]   Expansion of the genetic code enables design of a novel "gold'' class of green fluorescent proteins [J].
Bae, JH ;
Rubini, M ;
Jung, G ;
Wiegand, G ;
Seifert, MHJ ;
Azim, MK ;
Kim, JS ;
Zumbusch, A ;
Holak, TA ;
Moroder, L ;
Huber, R ;
Budisa, N .
JOURNAL OF MOLECULAR BIOLOGY, 2003, 328 (05) :1071-1081
[9]   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
[10]  
BALDWIN AN, 1966, J BIOL CHEM, V241, P839