Wang Qian, Parrish Angela R, Wang Lei
The Jack H. Skirball Center for Chemical Biology and Proteomics, The Salk Institute for Biological Studies, 10010 North Torrey Pines Road, La Jolla, CA 92037, USA.
Chem Biol. 2009 Mar 27;16(3):323-36. doi: 10.1016/j.chembiol.2009.03.001.
Using an orthogonal tRNA-synthetase pair, unnatural amino acids can be genetically encoded with high efficiency and fidelity, and over 40 unnatural amino acids have been site-specifically incorporated into proteins in Escherichia coli, yeast, or mammalian cells. Novel chemical or physical properties embodied in these amino acids enable new means for tailored manipulation of proteins. This review summarizes the methodology and recent progress in expanding this technology to eukaryotic cells. Applications of genetically encoded unnatural amino acids are highlighted with reports on labeling and modifying proteins, probing protein structure and function, identifying and regulating protein activity, and generating proteins with new properties. Genetic incorporation of unnatural amino acids provides a powerful method for investigating a wide variety of biological processes both in vitro and in vivo.
利用一对正交的tRNA-合成酶,可以高效且保真地对非天然氨基酸进行遗传编码,并且已有40多种非天然氨基酸被位点特异性地掺入大肠杆菌、酵母或哺乳动物细胞的蛋白质中。这些氨基酸所具有的新型化学或物理特性为蛋白质的定制操作提供了新方法。本综述总结了将该技术扩展到真核细胞的方法及最新进展。通过对蛋白质进行标记和修饰、探究蛋白质结构与功能、鉴定和调节蛋白质活性以及生成具有新特性的蛋白质的相关报道,突出了遗传编码非天然氨基酸的应用。非天然氨基酸的遗传掺入为在体外和体内研究多种生物学过程提供了一种强大的方法。