Wang Kaihang, Neumann Heinz, Peak-Chew Sew Y, Chin Jason W
Medical Research Council Laboratory of Molecular Biology, Hills Road, Cambridge CB2 2QH, England, UK.
Nat Biotechnol. 2007 Jul;25(7):770-7. doi: 10.1038/nbt1314. Epub 2007 Jun 24.
In vivo incorporation of unnatural amino acids by amber codon suppression is limited by release factor-1-mediated peptide chain termination. Orthogonal ribosome-mRNA pairs function in parallel with, but independent of, natural ribosomes and mRNAs. Here we show that an evolved orthogonal ribosome (ribo-X) improves tRNA(CUA)-dependent decoding of amber codons placed in orthogonal mRNA. By combining ribo-X, orthogonal mRNAs and orthogonal aminoacyl-tRNA synthetase/tRNA pairs in Escherichia coli, we increase the efficiency of site-specific unnatural amino acid incorporation from approximately 20% to >60% on a single amber codon and from <1% to >20% on two amber codons. We hypothesize that these increases result from a decreased functional interaction of the orthogonal ribosome with release factor-1. This technology should minimize the functional and phenotypic effects of truncated proteins in experiments that use unnatural amino acid incorporation to probe protein function in vivo.
通过琥珀密码子抑制实现的非天然氨基酸的体内掺入受到释放因子-1介导的肽链终止的限制。正交核糖体-mRNA对与天然核糖体和mRNA并行发挥作用,但相互独立。在此,我们表明,一种经过进化的正交核糖体(核糖体-X)提高了位于正交mRNA中的琥珀密码子的tRNA(CUA)依赖性解码效率。通过在大肠杆菌中组合核糖体-X、正交mRNA和正交氨酰-tRNA合成酶/tRNA对,我们将单个琥珀密码子位点特异性非天然氨基酸掺入的效率从约20%提高到>60%,将两个琥珀密码子的掺入效率从<1%提高到>20%。我们推测,这些提高是由于正交核糖体与释放因子-1之间功能相互作用的降低。在利用非天然氨基酸掺入来体内探测蛋白质功能的实验中,这项技术应能将截短蛋白的功能和表型效应降至最低。