Exploring the Limits of Codon and Anticodon Size
Overview
Biology
Chemistry
Affiliations
We previously employed a combinatorial approach to identify the most efficient suppressors of four-base codons in E. coli. We have now examined the suppression of two-, three-, four-, five-, and six-base codons with tRNAs containing 6-10 nt in their anticodon loops. We found that the E. coli translational machinery tolerates codons of 3-5 bases and that tRNAs with 6-10 nt anticodon loops can suppress these codons. However, N-length codons were found to prefer N + 4-length anticodon loops. Additionally, sequence preferences, including the requirement of Watson-Crick complementarity to the codon, were evident in the loops. These selections have yielded efficient suppressors of four-base and five-base codons for our ongoing efforts to expand the genetic code. They also highlight some of the parameters that underlie the fidelity of frame maintenance.
Toward a Quadruplet Codon Mitochondrial Genetic Code.
Pigula M, Ban Y, Schultz P ACS Synth Biol. 2024; 13(12):4175-4179.
PMID: 39631441 PMC: 11792677. DOI: 10.1021/acssynbio.4c00630.
Cellular Site-Specific Incorporation of Noncanonical Amino Acids in Synthetic Biology.
Niu W, Guo J Chem Rev. 2024; 124(18):10577-10617.
PMID: 39207844 PMC: 11470805. DOI: 10.1021/acs.chemrev.3c00938.
Evolution of Pyrrolysyl-tRNA Synthetase: From Methanogenesis to Genetic Code Expansion.
Koch N, Budisa N Chem Rev. 2024; 124(16):9580-9608.
PMID: 38953775 PMC: 11363022. DOI: 10.1021/acs.chemrev.4c00031.
Engineering tRNAs for the Ribosomal Translation of Non-proteinogenic Monomers.
Sigal M, Matsumoto S, Beattie A, Katoh T, Suga H Chem Rev. 2024; 124(10):6444-6500.
PMID: 38688034 PMC: 11122139. DOI: 10.1021/acs.chemrev.3c00894.
Non-Canonical Amino Acids in Analyses of Protease Structure and Function.
Goettig P, Koch N, Budisa N Int J Mol Sci. 2023; 24(18).
PMID: 37762340 PMC: 10531186. DOI: 10.3390/ijms241814035.