Sense codon reassignment enables viral resistance and encoded polymer synthesis

Author:

Robertson Wesley E.1ORCID,Funke Louise F. H.1ORCID,de la Torre Daniel1ORCID,Fredens Julius1ORCID,Elliott Thomas S.1,Spinck Martin1ORCID,Christova Yonka1ORCID,Cervettini Daniele1ORCID,Böge Franz L.1,Liu Kim C.1ORCID,Buse Salvador1ORCID,Maslen Sarah1ORCID,Salmond George P. C.2,Chin Jason W.1ORCID

Affiliation:

1. Medical Research Council Laboratory of Molecular Biology, Cambridge, UK.

2. Department of Biochemistry, University of Cambridge, Cambridge, UK.

Abstract

Designing bacterial superpowers Biological systems read all 64 triplet codons in DNA to encode the synthesis of proteins composed of 20 canonical amino acids. Robertson et al. created cells that do not read several codons and showed that this confers complete resistance to viruses, which normally rely on the host cell's ability to read all the codons in the viral genome to reproduce (see the Perspective by Jewel and Chatterjee). The authors reassigned each codon to several noncanonical amino acids (ncAAs). This advance enables the efficient synthesis of proteins containing three distinct ncAAs and the encoded synthesis of entirely noncanonical polymers and macrocycles. Science , abg3029, this issue p. 1057 ; see also abi9892, p. 1040

Funder

Medical Research Council

European Research Council

Development Gap Fund Award

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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