Signalling Research Centres BIOSS and CIBSS, University of Freiburg, Schänzlestr. 18, 79104, Freiburg, Germany.
Institute of Biology II, Faculty of Biology, University of Freiburg, Schänzlestr. 1, 79104, Freiburg, Germany.
Nucleic Acids Res. 2024 Jan 5;52(D1):D476-D482. doi: 10.1093/nar/gkad1090.
The incorporation of non-canonical amino acids (ncAAs) into proteins is a powerful technique used in various research fields. Genetic code expansion (GCE) is the most common way to achieve this: a specific codon is selected to be decoded by a dedicated tRNA orthogonal to the endogenous ones. In the past 30 years, great progress has been made to obtain novel tRNA synthetases (aaRSs) accepting a variety of ncAAs with distinct physicochemical properties, to develop robust in vitro assays or approaches for codon reassignment. This sparked the use of the technique, leading to the accumulation of publications, from which gathering all relevant information can appear daunting. Here we present iNClusive (https://non-canonical-aas.biologie.uni-freiburg.de/), a manually curated, extensive repository using standardized nomenclature that provides organized information on ncAAs successfully incorporated into target proteins as verified by mass spectrometry. Since we focused on tRNA synthetase-based tRNA loading, we provide the sequence of the tRNA and aaRS used for the incorporation. Derived from more than 687 peer-reviewed publications, it currently contains 2432 entries about 466 ncAAs, 569 protein targets, 500 aaRSs and 144 tRNAs. We foresee iNClusive will encourage more researchers to experiment with ncAA incorporation thus contributing to the further development of this exciting technique.
非天然氨基酸(ncAAs)的掺入是一种广泛应用于各个研究领域的强大技术。遗传密码扩展(GCE)是实现这一目标的最常见方法:选择一个特定的密码子,由与内源性 tRNA 正交的专用 tRNA 进行解码。在过去的 30 年中,人们在获得能够接受各种具有独特物理化学性质的 ncAAs 的新型 tRNA 合成酶(aaRS)方面取得了巨大进展,开发了用于密码子重新分配的稳健的体外测定或方法。这激发了该技术的应用,导致相关出版物的积累,从中收集所有相关信息可能会令人望而却步。在这里,我们介绍了 iNClusive(https://non-canonical-aas.biologie.uni-freiburg.de/),这是一个手动整理的、广泛的存储库,使用标准化命名法提供了成功掺入目标蛋白中的 ncAAs 的组织信息,这些信息已通过质谱验证。由于我们专注于基于 tRNA 合成酶的 tRNA 加载,因此我们提供了用于掺入的 tRNA 和 aaRS 的序列。它源自 687 多篇同行评议的出版物,目前包含 2432 条关于 466 种 ncAAs、569 种蛋白质靶标、500 种 aaRS 和 144 种 tRNA 的信息。我们预计,iNClusive 将鼓励更多的研究人员尝试 ncAA 掺入,从而为这一令人兴奋的技术的进一步发展做出贡献。