Xue Hong, Wong J Tze-Fei
Division of Life Science and Applied Genomics Center, Hong Kong University of Science & Technology, Clear Water Bay, Hong Kong, China.
Life (Basel). 2017 Feb 28;7(1):10. doi: 10.3390/life7010010.
The methods for establishing synthetic lifeforms with rewritten genetic codes comprising non-canonical amino acids (NCAA) in addition to canonical amino acids (CAA) include proteome-wide replacement of CAA, insertion through suppression of nonsense codon, and insertion via the pyrrolysine and selenocysteine pathways. Proteome-wide reassignments of nonsense codons and sense codons are also under development. These methods enable the application of NCAAs to enrich both fundamental and applied aspects of protein chemistry and biology. Sense codon reassignment to NCAA could incur problems arising from the usage of anticodons as identity elements on tRNA, and possible misreading of NNY codons by UNN anticodons. Evidence suggests that the problem of anticodons as identity elements can be diminished or resolved through removal from the tRNA of all identity elements besides the anticodon, and the problem of misreading of NNY codons by UNN anticodon can be resolved by the retirement of both the UNN anticodon and its complementary NNA codon from the proteome in the event that a restrictive post-transcriptional modification of the UNN anticodon by host enzymes to prevent the misreading cannot be obtained.
建立除了标准氨基酸(CAA)之外还包含非标准氨基酸(NCAA)的重写遗传密码的合成生命形式的方法包括在整个蛋白质组范围内替换CAA、通过抑制无义密码子进行插入以及通过吡咯赖氨酸和硒代半胱氨酸途径进行插入。无义密码子和有义密码子在整个蛋白质组范围内的重新分配也在开发中。这些方法能够应用NCAA来丰富蛋白质化学和生物学的基础及应用方面。将有义密码子重新分配给NCAA可能会引发因将反密码子用作tRNA上的识别元件而产生的问题,以及UNN反密码子可能误读NNY密码子的问题。有证据表明,通过从tRNA中去除除反密码子之外的所有识别元件,可以减少或解决将反密码子用作识别元件的问题;如果无法通过宿主酶对UNN反密码子进行限制性转录后修饰来防止误读,那么在蛋白质组中同时去除UNN反密码子及其互补的NNA密码子,就可以解决UNN反密码子误读NNY密码子的问题。