Non-standard amino acid incorporation into proteins using Escherichia coli cell-free protein synthesis

被引:86
作者
Hong, Seok Hoon [1 ,2 ]
Kwon, Yong-Chan [1 ,2 ]
Jewett, Michael C. [1 ,2 ,3 ,4 ]
机构
[1] Northwestern Univ, Chem & Biol Engn, 2145 Sheridan Rd,Tech E-136, Evanston, IL 60208 USA
[2] Northwestern Univ, Chem Life Proc Inst, Evanston, IL USA
[3] Northwestern Univ, Robert H Lurie Comprehens Canc Ctr, Chicago, IL 60611 USA
[4] Northwestern Univ, Inst Bionanotechnol Med, Chicago, IL 60611 USA
基金
美国国家科学基金会;
关键词
non-standard amino acids; cell-free protein synthesis; synthetic biology; sequence-defined polymers; genome engineering; TRANSFER-RNA SYNTHETASE; SITE-SPECIFIC INCORPORATION; ORTHOGONAL TRANSFER-RNA; EXPANDED GENETIC-CODE; IN-VITRO; UNNATURAL PEPTIDES; FREE TRANSLATION; DE-NOVO; SYSTEM; MULTIPLE;
D O I
10.3389/fchem.2014.00034
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Incorporating non-standard amino acids (NSAAs) into proteins enables new chemical properties, new structures, and new functions. In recent years, improvements in cell -free protein synthesis (CFPS) systems have opened the way to accurate and efficient incorporation of NSAAs into proteins. The driving force behind this development has been three -fold. First, a technical renaissance has enabled high -yielding (>1 g/L) and long-lasting (>10 h in batch operation) CFPS in systems derived from Escherichia colt Second, the efficiency of orthogonal translation systems (OTSs) has improved. Third, the open nature of the CFPS platform has brought about an unprecedented level of control and freedom of design. Here, we review recent developments in CFPS platforms designed to precisely incorporate NSAAs. In the coming years, we anticipate that CFPS systems will impact efforts to elucidate structure/function relationships of proteins and to make biomaterials and sequence -defined biopolymers for medical and industrial applications.
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页数:7
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