Recoded gene circuits for multiplexed genetic code expansion
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Publisher
Springer Science and Business Media LLC
Link
https://www.nature.com/articles/s41587-024-02387-w.pdf
Reference5 articles.
1. Noren, C. J., Anthony-Cahill, S. J., Griffith, M. C. & Schultz, P. G. A general method for site-specific incorporation of unnatural amino acids into proteins. Science 244, 182–188 (1989). This seminal paper from the Schultz Lab describes the first use of amber suppression to site-specifically incorporate a non-canonical amino acid.
2. Dunkelmann, D. L., Oehm, S. B., Beattie, A. T. & Chin, J. W. A 68-codon genetic code to incorporate four distinct non-canonical amino acids enabled by automated orthogonal mRNA design. Nat. Chem. 13, 1110–1117 (2021). This paper describes quadruplet decoding with orthogonal ribosomes.
3. DeBenedictis, E. A., Carver, G. D., Chung, C. Z., Soll, D. & Badran, A. H. Multiplex suppression of four quadruplet codons via tRNA directed evolution. Nat. Commun. 12, 5706 (2021). This paper describes our previous efforts to decode quadruplet codons with E. coli tRNAs.
4. Costello, A. & Badran, A. H. Synthetic biological circuits within an orthogonal central dogma. Trends Biotechnol. 39, 59–71 (2021). This perspective article highlights the importance of orthogonality in genetic circuits aiming to expand the central dogma.
5. Townend, J. E. & Tavassoli, A. Traceless production of cyclic peptide libraries in E. coli. ACS Chem. Biol. 11, 1624–1630 (2016). This paper developed the split-intein system for circular ligation of peptides and proteins we adapted for peptide macrocyclization.
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