In Situ Deprotection and Incorporation of Unnatural Amino Acids during Cell‐Free Protein Synthesis |
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Authors: | Dr Isaac N Arthur Dr James E Hennessy Dr Dharshana Padmakshan Dr Dannon J Stigers Stéphanie Lesturgez Samuel A Fraser Mantas Liutkus Prof Gottfried Otting Dr John G Oakeshott Prof Christopher J Easton |
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Institution: | 1. Research School of Chemistry, Australian National University, Canberra, ACT 0200 (Australia), Fax: (+61)?2‐6125‐8114;2. ARC Centre of Excellence for Free Radical Chemistry and Biotechnology, Australian National University, Canberra, ACT 0200 (Australia);3. CSIRO Ecosystem Sciences, Canberra, ACT 2601 (Australia) |
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Abstract: | The S30 extract from E. coli BL21 Star (DE3) used for cell‐free protein synthesis removes a wide range of α‐amino acid protecting groups by cleaving α‐carboxyl hydrazides; methyl, benzyl, tert‐butyl, and adamantyl esters; tert‐butyl and adamantyl carboxamides; α‐amino form‐, acet‐, trifluoroacet‐, and benzamides; and side‐chain hydrazides and esters. The free amino acids are produced and incorporated into a protein under standard conditions. This approach allows the deprotection of amino acids to be carried out in situ to avoid separate processing steps. The advantages of this approach are demonstrated by the efficient incorporation of the chemically intractable (S)‐4‐fluoroleucine, (S)‐4,5‐dehydroleucine, and (2S,3R)‐4‐chlorovaline into a protein through the direct use of their respective precursors, namely, (S)‐4‐fluoroleucine hydrazide, (S)‐4,5‐dehydroleucine hydrazide, and (2S,3R)‐4‐chlorovaline methyl ester. These results also show that the fluoro‐ and dehydroleucine and the chlorovaline are incorporated into a protein by the normal biosynthetic machinery as substitutes for leucine and isoleucine, respectively. |
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Keywords: | amino acids cell‐free synthesis enzyme catalysis protecting groups protein expression |
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