Synthetic mimics of protein surfaces have the potential to become inhibitors of protein protein interactions or. even synthetic vaccines. However, the synthesis of these complicated molecular constructs is still difficult. Here we describe an. efficient and versatile synthesis of protein mimics containing up to three different cyclic peptides. Using a sequential native chemical ligation strategy, peptide loops containing a thioester handle were introduced onto a triazacyclophane scaffold bearing orthogonal protected cysteine residues.
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Univ Manchester, Sch Chem, Manchester M17DN, Lancs, England
Univ Manchester, Manchester Interdisciplinary Bioctr, Manchester M17DN, Lancs, EnglandUniv Kiel, Otto Diels Inst Organ Chem, D-24098 Kiel, Germany
Weissenborn, Martin J.
Castangia, Roberto
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Univ Manchester, Sch Chem, Manchester M17DN, Lancs, England
Univ Manchester, Manchester Interdisciplinary Bioctr, Manchester M17DN, Lancs, EnglandUniv Kiel, Otto Diels Inst Organ Chem, D-24098 Kiel, Germany
Castangia, Roberto
Wehner, Johannes W.
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Univ Kiel, Otto Diels Inst Organ Chem, D-24098 Kiel, GermanyUniv Kiel, Otto Diels Inst Organ Chem, D-24098 Kiel, Germany
Wehner, Johannes W.
Sardzik, Robert
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Univ Manchester, Sch Chem, Manchester M17DN, Lancs, England
Univ Manchester, Manchester Interdisciplinary Bioctr, Manchester M17DN, Lancs, EnglandUniv Kiel, Otto Diels Inst Organ Chem, D-24098 Kiel, Germany
Sardzik, Robert
Lindhorst, Thisbe K.
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Univ Kiel, Otto Diels Inst Organ Chem, D-24098 Kiel, GermanyUniv Kiel, Otto Diels Inst Organ Chem, D-24098 Kiel, Germany
Lindhorst, Thisbe K.
Flitsch, Sabine L.
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Univ Manchester, Sch Chem, Manchester M17DN, Lancs, England
Univ Manchester, Manchester Interdisciplinary Bioctr, Manchester M17DN, Lancs, EnglandUniv Kiel, Otto Diels Inst Organ Chem, D-24098 Kiel, Germany