Genetic Encoding of Cyanopyridylalanine for In-Cell Protein Macrocyclization by the Nitrile-Aminothiol Click Reaction
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Authors
Abdelkader, Elwy
Qianzhu, Haocheng
George, Josemon
Frkic, Rebecca
Jackson, Colin
Nitsche, Christoph
Otting, Gottfried
Huber, Thomas
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Wiley
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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Angewandte Chemie
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Open Access
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Creative Commons Attribution Non-Commercial NoDerivs License