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Dual stop codon suppression in mammalian cells with genomically integrated genetic code expansion machinery.


ABSTRACT: Stop codon suppression using dedicated tRNA/aminoacyl-tRNA synthetase (aaRS) pairs allows for genetically encoded, site-specific incorporation of non-canonical amino acids (ncAAs) as chemical handles for protein labeling and modification. Here, we demonstrate that piggyBac-mediated genomic integration of archaeal pyrrolysine tRNA (tRNAPyl)/pyrrolysyl-tRNA synthetase (PylRS) or bacterial tRNA/aaRS pairs, using a modular plasmid design with multi-copy tRNA arrays, allows for homogeneous and efficient genetically encoded ncAA incorporation in diverse mammalian cell lines. We assess opportunities and limitations of using ncAAs for fluorescent labeling applications in stable cell lines. We explore suppression of ochre and opal stop codons and finally incorporate two distinct ncAAs with mutually orthogonal click chemistries for site-specific, dual-fluorophore labeling of a cell surface receptor on live mammalian cells.

SUBMITTER: Meineke B 

PROVIDER: S-EPMC10694491 | biostudies-literature | 2023 Nov

REPOSITORIES: biostudies-literature

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Dual stop codon suppression in mammalian cells with genomically integrated genetic code expansion machinery.

Meineke Birthe B   Heimgärtner Johannes J   Caridha Rozina R   Block Matthias F MF   Kimler Kyle J KJ   Pires Maria F MF   Landreh Michael M   Elsässer Simon J SJ  

Cell reports methods 20231106 11


Stop codon suppression using dedicated tRNA/aminoacyl-tRNA synthetase (aaRS) pairs allows for genetically encoded, site-specific incorporation of non-canonical amino acids (ncAAs) as chemical handles for protein labeling and modification. Here, we demonstrate that piggyBac-mediated genomic integration of archaeal pyrrolysine tRNA (tRNA<sup>Pyl</sup>)/pyrrolysyl-tRNA synthetase (PylRS) or bacterial tRNA/aaRS pairs, using a modular plasmid design with multi-copy tRNA arrays, allows for homogeneous  ...[more]

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