Medical Research Council Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge CB2 0QH, England, United Kingdom.
Max Planck Institute of Molecular Plant Physiology, Am Mühlenberg 1, 14476 Potsdam-Golm, Germany.
Chem Rev. 2024 Oct 9;124(19):11008-11062. doi: 10.1021/acs.chemrev.4c00243. Epub 2024 Sep 5.
Over the past 16 years, genetic code expansion and reprogramming in living organisms has been transformed by advances that leverage the unique properties of pyrrolysyl-tRNA synthetase (PylRS)/tRNA pairs. Here we summarize the discovery of the pyrrolysine system and describe the unique properties of PylRS/tRNA pairs that provide a foundation for their transformational role in genetic code expansion and reprogramming. We describe the development of genetic code expansion, from to all domains of life, using PylRS/tRNA pairs, and the development of systems that biosynthesize and incorporate ncAAs using pyl systems. We review applications that have been uniquely enabled by the development of PylRS/tRNA pairs for incorporating new noncanonical amino acids (ncAAs), and strategies for engineering PylRS/tRNA pairs to add noncanonical monomers, beyond α--amino acids, to the genetic code of living organisms. We review rapid progress in the discovery and scalable generation of mutually orthogonal PylRS/tRNA pairs that can be directed to incorporate diverse ncAAs in response to diverse codons, and we review strategies for incorporating multiple distinct ncAAs into proteins using mutually orthogonal PylRS/tRNA pairs. Finally, we review recent advances in the encoded cellular synthesis of noncanonical polymers and macrocycles and discuss future developments for PylRS/tRNA pairs.
在过去的 16 年中,通过利用吡咯赖氨酰-tRNA 合成酶(PylRS)/tRNA 对的独特性质的进展,活生物体中的遗传密码扩展和重编程发生了转变。在这里,我们总结了吡咯赖氨酸系统的发现,并描述了 PylRS/tRNA 对的独特性质,这些性质为它们在遗传密码扩展和重编程中的变革作用提供了基础。我们描述了遗传密码扩展的发展,从到所有生命领域,使用 PylRS/tRNA 对,以及使用 pyl 系统生物合成和掺入 ncAA 的系统的发展。我们回顾了由于 PylRS/tRNA 对用于掺入新的非典型氨基酸(ncAA)的开发而得以独特实现的应用,并回顾了用于工程化 PylRS/tRNA 对的策略,以将非典型单体(超出 α--氨基酸)添加到活生物体的遗传密码中。我们回顾了在发现和可扩展生成互斥的 PylRS/tRNA 对方面的快速进展,这些对可以响应不同的密码子来指导掺入不同的 ncAA,我们还回顾了使用互斥的 PylRS/tRNA 对将多个不同的 ncAA 掺入蛋白质中的策略。最后,我们回顾了最近在非典型聚合物和大环的细胞内合成方面的进展,并讨论了 PylRS/tRNA 对的未来发展。