Department of Chemistry, Graduate School of Science, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.
Int J Mol Sci. 2019 Jan 26;20(3):522. doi: 10.3390/ijms20030522.
Methods of genetic code manipulation, such as nonsense codon suppression and genetic code reprogramming, have enabled the incorporation of various nonproteinogenic amino acids into the peptide nascent chain. However, the incorporation efficiency of such amino acids largely varies depending on their structural characteristics. For instance, l-α-amino acids with artificial, bulky side chains are poorer substrates for ribosomal incorporation into the nascent peptide chain, mainly owing to the lower affinity of their aminoacyl-tRNA toward elongation factor-thermo unstable (EF-Tu). Phosphorylated Ser and Tyr are also poorer substrates for the same reason; engineering EF-Tu has turned out to be effective in improving their incorporation efficiencies. On the other hand, exotic amino acids such as d-amino acids and β-amino acids are even poorer substrates owing to their low affinity to EF-Tu and poor compatibility to the ribosome active site. Moreover, their consecutive incorporation is extremely difficult. To solve these problems, the engineering of ribosomes and tRNAs has been executed, leading to successful but limited improvement of their incorporation efficiency. In this review, we comprehensively summarize recent attempts to engineer the translation systems, resulting in a significant improvement of the incorporation of exotic amino acids.
遗传密码操纵方法,如无义密码子抑制和遗传密码重编程,已经能够将各种非天然氨基酸掺入肽新生链中。然而,这些氨基酸的掺入效率在很大程度上取决于它们的结构特征。例如,具有人工、庞大侧链的 l-α-氨基酸作为核糖体掺入新生肽链的底物较差,主要是由于它们的氨酰-tRNA 对伸长因子-热不稳定(EF-Tu)的亲和力较低。磷酸化的 Ser 和 Tyr 也由于同样的原因成为较差的底物;工程化 EF-Tu 已被证明在提高它们的掺入效率方面是有效的。另一方面,由于与 EF-Tu 的亲和力低以及与核糖体活性位点的兼容性差,外来氨基酸,如 d-氨基酸和β-氨基酸,甚至是较差的底物。此外,它们的连续掺入极其困难。为了解决这些问题,已经对核糖体和 tRNA 进行了工程改造,导致它们的掺入效率得到了成功但有限的提高。在这篇综述中,我们全面总结了最近在改造翻译系统方面的尝试,这些尝试显著提高了外来氨基酸的掺入效率。