Chemical Conjugation to Less Targeted Proteinogenic Amino Acids

Chembiochem. 2022 Oct 6;23(19):e202200245. doi: 10.1002/cbic.202200245. Epub 2022 Jul 20.

Abstract

Protein bioconjugates are in high demand for applications in biomedicine, diagnostics, chemical biology and bionanotechnology. Proteins are large and sensitive molecules containing multiple different functional groups and in particular nucleophilic groups. In bioconjugation reactions it can therefore be challenging to obtain a homogeneous product in high yield. Numerous strategies for protein conjugation have been developed, of which a vast majority target lysine, cysteine and to a lesser extend tyrosine. Likewise, several methods that involve recombinantly engineered protein tags have been reported. In recent years a number of methods have emerged for chemical bioconjugation to other amino acids and in this review, we present the progress in this area.

Keywords: bioconjugation; chemical protein labeling; protein conjugation; protein modifications; site-specific conjugation.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amines
  • Amino Acids* / chemistry
  • Cysteine*
  • Lysine
  • Proteins / chemistry
  • Tyrosine

Substances

  • Amines
  • Amino Acids
  • Proteins
  • Tyrosine
  • Lysine
  • Cysteine