Quintuply orthogonal pyrrolysyl-tRNA synthetase/tRNA pairs.

Nat Chem

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

Published: July 2023

AI Article Synopsis

  • Researchers have developed quintuply orthogonal pairs of pyrrolysyl-tRNA synthetase (PylRS) and pyrrolysyl-tRNA (tRNA), expanding the ability to incorporate non-canonical amino acids into proteins.
  • They established sequence identity thresholds for mutual orthogonality, leading to the identification of five classes of PylRS/tRNA pairs through clustering.
  • The study successfully created a vast number of orthogonal PylRS/tRNA combinations, paving the way for advancing encoded polymer synthesis and enhancing protein engineering.

Article Abstract

Mutually orthogonal aminoacyl transfer RNA synthetase/transfer RNA pairs provide a foundation for encoding non-canonical amino acids into proteins, and encoded non-canonical polymer and macrocycle synthesis. Here we discover quintuply orthogonal pyrrolysyl-tRNA synthetase (PylRS)/pyrrolysyl-tRNA (tRNA) pairs. We discover empirical sequence identity thresholds for mutual orthogonality and use these for agglomerative clustering of PylRS and tRNA sequences; this defines numerous sequence clusters, spanning five classes of PylRS/tRNA pairs (the existing classes +N, A and B, and newly defined classes C and S). Most of the PylRS clusters belong to classes that were unexplored for orthogonal pair generation. By testing pairs from distinct clusters and classes, and pyrrolysyl-tRNAs with unusual structures, we resolve 80% of the pairwise specificities required to make quintuply orthogonal PylRS/tRNA pairs; we control the remaining specificities by engineering and directed evolution. Overall, we create 924 mutually orthogonal PylRS/tRNA pairs, 1,324 triply orthogonal pairs, 128 quadruply orthogonal pairs and 8 quintuply orthogonal pairs. These advances may provide a key foundation for encoded polymer synthesis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7615293PMC
http://dx.doi.org/10.1038/s41557-023-01232-yDOI Listing

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