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In this study, we reassigned the initiator fMet to ClAc L Y ( N -chloroacetyl-L-Tyr) or ClAc D Y ( N -chloroacetyl-D-Tyr) in the FIT system and used an mRNA library with a complexity of 10 14 that was designed to have random sequences designated by (NNK) n , ( n =415) flanked by the initiator AUG (ClAc L/D Y) and UGC (Cys) codons, followed by a short linker peptide

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[DOI] [PubMed] [Google Scholar] 3.Siekmann JH, Allen LH, Bwibo NO, Demment MW, Murphy SP, Neumann CG