Abstract
Cyanopyridylalanines are non-canonical amino acids that react with aminothiol compounds under physiological conditions in a biocompatible manner without requiring added catalyst. Here we present newly developed aminoacyl-tRNA synthetases for genetic encoding of meta- and para-cyanopyridylalanine to enable the site-specific attachment of a wide range of different functionalities. The outstanding utility of the cyanopyridine moiety is demonstrated by examples of i) post-translational functionalization of proteins, ii) in-cell macrocyclization of peptides and proteins, and iii) protein stapling. The biocompatible nature of the protein ligation chemistry enabled by the cyanopyridylalanine amino acid opens a new path to specific in vivo protein modifications in complex biological environments.
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Abdelkader, E. H., Qianzhu, H., George, J., Frkic, R. L., Jackson, C. J., Nitsche, C., … Huber, T. (2022). Genetic Encoding of Cyanopyridylalanine for In-Cell Protein Macrocyclization by the Nitrile–Aminothiol Click Reaction. Angewandte Chemie - International Edition, 61(13). https://doi.org/10.1002/anie.202114154
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