Enhancing Protein Stability with Genetically Encoded Noncanonical Amino Acids

Jack C. Li, Tao Liu, Yan Wang, Angad P. Mehta, Peter G. Schultz

Research output: Contribution to journalArticlepeer-review

Abstract

The ability to add noncanonical amino acids to the genetic code may allow one to evolve proteins with new or enhanced properties using a larger set of building blocks. To this end, we have been able to select mutant proteins with enhanced thermal properties from a library of E. coli homoserine O-succinyltransferase (metA) mutants containing randomly incorporated noncanonical amino acids. Here, we show that substitution of Phe 21 with (p-benzoylphenyl)alanine (pBzF), increases the melting temperature of E. coli metA by 21 °C. This dramatic increase in thermal stability, arising from a single mutation, likely results from a covalent adduct between Cys 90 and the keto group of pBzF that stabilizes the dimeric form of the enzyme. These experiments show that an expanded genetic code can provide unique solutions to the evolution of proteins with enhanced properties.

Original languageEnglish (US)
Pages (from-to)15997-16000
Number of pages4
JournalJournal of the American Chemical Society
Volume140
Issue number47
DOIs
StatePublished - Nov 28 2018
Externally publishedYes

ASJC Scopus subject areas

  • Catalysis
  • Chemistry(all)
  • Biochemistry
  • Colloid and Surface Chemistry

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