Efficient Synthesis of Protein Mimics by Sequential Native Chemical Ligation

被引:8
|
作者
van de Langemheen, Helmus [1 ]
van Ufford, H. C. Quarles [1 ]
Kruijtzer, John A. W. [1 ]
Liskamp, Rob M. J. [1 ,2 ]
机构
[1] Univ Utrecht, Fac Sci, Utrecht Inst Pharmaceut Sci, Dept Pharmaceut Sci, NL-3508 TB Utrecht, Netherlands
[2] Univ Glasgow, Sch Chem, Glasgow G12 8QQ, Lanark, Scotland
关键词
ARTIFICIAL RECEPTORS; SOLID-PHASE; SCAFFOLD; GP120; RECOMBINANT; PEPTIDES; EPITOPES; STRATEGY; DESIGN; LOOPS;
D O I
10.1021/ol500604h
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
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.
引用
收藏
页码:2138 / 2141
页数:4
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