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pubmed-article:17150804pubmed:abstractTextHere we describe a de novo tRNA acylation system consisting of artificial ribozymes. This system, the flexizyme (Fx) system, allows for the preparation of acyl-tRNAs with almost no limitation on the use of a variety of amino/hydroxy acids and tRNAs. To demonstrate its utility, we have carried out protein synthesis involving site-specific incorporation of nonnatural amino and hydroxy acids via amber or programmed frame-shift suppressions. We have also demonstrated peptide synthesis involving multiple nonnatural amino acids via sense codon suppression. The combination of the Fx system and appropriate cell-free translation is a powerful and flexible tool for mRNA-encoded synthesis of nonnatural polypeptides.lld:pubmed
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pubmed-article:17150804pubmed:authorpubmed-author:MurakamiHiros...lld:pubmed
pubmed-article:17150804pubmed:authorpubmed-author:SugaHiroakiHlld:pubmed
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pubmed-article:17150804pubmed:authorpubmed-author:SakoYusukeYlld:pubmed
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pubmed-article:17150804pubmed:pagination35-6lld:pubmed
pubmed-article:17150804pubmed:dateRevised2007-9-19lld:pubmed
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pubmed-article:17150804pubmed:year2006lld:pubmed
pubmed-article:17150804pubmed:articleTitleFlexizyme as a versatile tRNA acylation catalyst and the application for translation.lld:pubmed
pubmed-article:17150804pubmed:affiliationResearch Center for Advanced Science and Technology, The University of Tokyo, 4-6-1 Komaba, Meguro-ku, Tokyo 153-8904, Japan.lld:pubmed
pubmed-article:17150804pubmed:publicationTypeJournal Articlelld:pubmed