Genetic Encoding of Cyanopyridylalanine for In-Cell Protein Macrocyclization by the Nitrile-Aminothiol Click Reaction

Angew Chem Int Ed Engl. 2022 Mar 21;61(13):e202114154. doi: 10.1002/anie.202114154. Epub 2022 Feb 11.

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.

Keywords: Bioorthogonal Reaction; Cyanopyridylalanine; Genetic Encoding; Noncanonical Amino Acids; Protein Conjugation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amines
  • Amino Acids / chemistry
  • Amino Acyl-tRNA Synthetases* / genetics
  • Amino Acyl-tRNA Synthetases* / metabolism
  • Nitriles*
  • Proteins / chemistry
  • Sulfhydryl Compounds

Substances

  • Amines
  • Amino Acids
  • Nitriles
  • Proteins
  • Sulfhydryl Compounds
  • Amino Acyl-tRNA Synthetases