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A synthetic tRNA for EF-Tu mediated selenocysteine incorporation in vivo and in vitro.


ABSTRACT: Incorporation of selenocysteine (Sec) in bacteria requires a UGA codon that is reassigned to Sec by the Sec-specific elongation factor SelB and a conserved mRNA motif (SECIS element). These requirements severely restrict the engineering of selenoproteins. Earlier, a synthetic tRNASec was reported that allowed canonical Sec incorporation by EF-Tu; however, serine misincorporation limited its scope. We report a superior tRNASec variant (tRNAUTuX) that facilitates EF-Tu dependent stoichiometric Sec insertion in response to UAG both in vivo in Escherichia coli and in vitro in a cellfree protein synthesis system. We also demonstrate recoding of several sense codons in a SelB supplemented cell-free system. These advances in Sec incorporation will aid rational design and directed evolution of selenoproteins.

SUBMITTER: Miller C 

PROVIDER: S-EPMC4782793 | biostudies-literature | 2015 Aug

REPOSITORIES: biostudies-literature

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A synthetic tRNA for EF-Tu mediated selenocysteine incorporation in vivo and in vitro.

Miller Corwin C   Bröcker Markus J MJ   Prat Laure L   Ip Kevan K   Chirathivat Napon N   Feiock Alexander A   Veszprémi Miklós M   Söll Dieter D  

FEBS letters 20150706 17


Incorporation of selenocysteine (Sec) in bacteria requires a UGA codon that is reassigned to Sec by the Sec-specific elongation factor SelB and a conserved mRNA motif (SECIS element). These requirements severely restrict the engineering of selenoproteins. Earlier, a synthetic tRNASec was reported that allowed canonical Sec incorporation by EF-Tu; however, serine misincorporation limited its scope. We report a superior tRNASec variant (tRNAUTuX) that facilitates EF-Tu dependent stoichiometric Sec  ...[more]

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