Elsässer Simon J
Science for Life Laboratory, Division of Translational Medicine and Chemical Biology, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.
Methods Mol Biol. 2018;1728:237-245. doi: 10.1007/978-1-4939-7574-7_15.
Noncanonical amino acid mutagenesis via amber suppression provides the means to tailor proteins inside living cells. A wide range of noncanonical amino acids have been incorporated using the Methanococcus pyrrolysyl-tRNA synthetase/tRNACUA (PylRS/PylT) in mammalian cell systems in proof of principle experiments, for (1) minimal genetically encoded fluorescence or affinity tagging, (2) photo-control of enzymes, (3) genetically encoded posttranslational protein modifications. We have developed a general and efficient method to genomically integrate the PylRS/PylT amber suppression machinery using PiggyBac-mediated transposition. A general protocol for the generation of stable amber suppression cell lines is described here. Using the modular plasmid system, homogenous and highly efficient amber suppression in a wide range of cell lines can be achieved.
通过琥珀抑制进行的非标准氨基酸诱变提供了在活细胞内定制蛋白质的方法。在原理验证实验中,已使用甲烷球菌吡咯赖氨酸 - tRNA合成酶/tRNACUA(PylRS/PylT)在哺乳动物细胞系统中掺入了多种非标准氨基酸,用于(1)最小化遗传编码的荧光或亲和标记,(2)酶的光控,(3)遗传编码的翻译后蛋白质修饰。我们开发了一种通用且高效的方法,利用PiggyBac介导的转座将PylRS/PylT琥珀抑制机制基因组整合。本文描述了生成稳定琥珀抑制细胞系的通用方案。使用模块化质粒系统,可以在广泛的细胞系中实现均匀且高效的琥珀抑制。