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Enzymes with noncanonical amino acids.
Zhao, Jingming; Burke, Ashleigh J; Green, Anthony P.
Affiliation
  • Zhao J; Manchester Institute of Biotechnology, School of Chemistry, University of Manchester, 131 Princess Street, Manchester M1 7DN, UK.
  • Burke AJ; Manchester Institute of Biotechnology, School of Chemistry, University of Manchester, 131 Princess Street, Manchester M1 7DN, UK.
  • Green AP; Manchester Institute of Biotechnology, School of Chemistry, University of Manchester, 131 Princess Street, Manchester M1 7DN, UK. Electronic address: anthony.green@manchester.ac.uk.
Curr Opin Chem Biol ; 55: 136-144, 2020 04.
Article in En | MEDLINE | ID: mdl-32163871
ABSTRACT
Enzyme design and engineering strategies rely almost exclusively on nature's alphabet of twenty canonical amino acids. Recent years have seen the emergence of powerful genetic code expansion methods that allow hundreds of structurally diverse amino acids to be installed into proteins in a site-selective manner. Here, we will highlight how the availability of an expanded alphabet of amino acids has opened new avenues in enzyme engineering research. Genetically encoded noncanonical amino acids have provided new tools to probe complex enzyme mechanisms, improve biocatalyst activity and stability, and most ambitiously to design enzymes with new catalytic mechanisms that would be difficult to access within the constraints of the genetic code. We anticipate that the studies highlighted in this article, coupled with the continuing advancements in genetic code expansion technology, will promote the widespread use of noncanonical amino acids in biocatalysis research in the coming years.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Enzymes / Amino Acids Language: En Journal: Curr Opin Chem Biol Journal subject: BIOQUIMICA Year: 2020 Document type: Article Affiliation country: Reino Unido

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Enzymes / Amino Acids Language: En Journal: Curr Opin Chem Biol Journal subject: BIOQUIMICA Year: 2020 Document type: Article Affiliation country: Reino Unido