4.6 Review

Versatility of Synthetic tRNAs in Genetic Code Expansion

Journal

GENES
Volume 9, Issue 11, Pages -

Publisher

MDPI
DOI: 10.3390/genes9110537

Keywords

genetic code expansion; transfer RNA; synthetic biology; non-canonical amino acids; selenocysteine

Funding

  1. US National Institutes of Health (NIH) [R35GM122560]
  2. US National Science Foundation [CHE-1740549]
  3. Division of Chemical Sciences, Geosciences, and Biosciences, Office of Basic Energy Sciences of the Department of Energy [DE-FG02-98ER20311]
  4. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R35GM122560] Funding Source: NIH RePORTER

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Transfer RNA (tRNA) is a dynamic molecule used by all forms of life as a key component of the translation apparatus. Each tRNA is highly processed, structured, and modified, to accurately deliver amino acids to the ribosome for protein synthesis. The tRNA molecule is a critical component in synthetic biology methods for the synthesis of proteins designed to contain non-canonical amino acids (ncAAs). The multiple interactions and maturation requirements of a tRNA pose engineering challenges, but also offer tunable features. Major advances in the field of genetic code expansion have repeatedly demonstrated the central importance of suppressor tRNAs for efficient incorporation of ncAAs. Here we review the current status of two fundamentally different translation systems (TSs), selenocysteine (Sec)- and pyrrolysine (Pyl)-TSs. Idiosyncratic requirements of each of these TSs mandate how their tRNAs are adapted and dictate the techniques used to select or identify the best synthetic variants.

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