Chemical insights into flexizyme-mediated tRNA acylation

Cell Chem Biol. 2022 Jul 21;29(7):1071-1112. doi: 10.1016/j.chembiol.2022.03.012. Epub 2022 Apr 11.

Abstract

A critical step in repurposing the cellular translation machinery for the synthesis of polymeric products is the acylation of transfer RNA (tRNA) with unnatural monomers. Toward this goal, flexizymes, ribozymes capable of aminoacylation, have emerged as a uniquely adept tool for charging tRNA with ever increasingly diverse substrates. In this review, we present a library of monomer substrates that have been tested for tRNA acylation with the flexizyme system. From this mile-high view, we provide insights for understanding the chemical factors that influence flexizyme-mediated tRNA acylation. We conclude that flexizymes are primitive esterification catalysts that display a modest binding affinity to the monomer's aromatic recognition element. Together, these robust, yet flexible, flexizyme systems provide researchers with unprecedented access for preparing unnatural acyl-tRNA and the opportunity to repurpose the translation machinery for the synthesis of novel biologically derived structures beyond native proteins and peptides.

Keywords: aminoacylation; flexizyme; genetic code; ribozymes; tRNA; translation.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't
  • Research Support, N.I.H., Extramural

MeSH terms

  • Acylation
  • Catalysis
  • Peptides / metabolism
  • RNA, Catalytic* / chemistry
  • RNA, Transfer / metabolism
  • Transfer RNA Aminoacylation*

Substances

  • Peptides
  • RNA, Catalytic
  • RNA, Transfer