Next-generation genetic code expansion

被引:52
|
作者
Arranz-Gibertt, Pol [1 ,2 ]
Vanderschurent, Koen [1 ,2 ]
Isaacs, Farren J. [1 ,2 ]
机构
[1] Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06520 USA
[2] Yale Univ, Syst Biol Inst, West Haven, CT 06516 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
TRANSFER-RNA SYNTHETASES; ELONGATION-FACTOR TU; SITE-SPECIFIC INCORPORATION; FREE PROTEIN-SYNTHESIS; UNNATURAL BASE-PAIR; D-AMINO ACIDS; IN-VIVO; ESCHERICHIA-COLI; SEMISYNTHETIC ORGANISM; RIBOSOMAL SYNTHESIS;
D O I
10.1016/j.cbpa.2018.07.020
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
Engineering of the translation apparatus has permitted the site specific incorporation of nonstandard amino acids (nsAAs) into proteins, thereby expanding the genetic code of organisms. Conventional approaches have focused on porting tRNAs and aminoacyl-tRNA synthetases (aaRS) from archaea into bacterial and eukaryotic systems where they have been engineered to site-specifically encode nsAAs. More recent work in genome engineering has opened up the possibilities of whole genome recoding, in which organisms with alternative genetic codes have been constructed whereby codons removed from the genetic code can be repurposed as new sense codons dedicated for incorporation of nsAAs. These advances, together with the advent of engineered ribosomes and new molecular evolution methods, enable multisite incorporation of nsAAs and nonstandard monomers (nsM) paving the way for the template-directed production of functionalized proteins, new classes of polymers, and genetically encoded materials.
引用
收藏
页码:203 / 211
页数:9
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