One-pot chemical synthesis of small ubiquitin-like modifier protein-peptide conjugates using bis(2-sulfanylethyl) amido peptide latent thioester surrogates

被引:51
作者
Boll, Emmanuelle [1 ]
Drobecq, Herve [1 ]
Ollivier, Nathalie [1 ]
Blanpain, Annick [1 ]
Raibaut, Laurent [1 ]
Desmet, Remi [1 ]
Vicogne, Jerome [1 ]
Melnyk, Oleg [1 ]
机构
[1] Univ Lille, CNRS, Inst Pasteur Lille, Lille Inst Biol, Lille, France
关键词
SOLID-PHASE SYNTHESIS; KINETICALLY CONTROLLED LIGATION; PSEUDO-PROLINES; DIFFICULT; OXAZOLIDINES; INSIGHTS; SUPPORT; SERINE; BOND;
D O I
10.1038/nprot.2015.013
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Small ubiquitin-like modifier (SUMO) post-translational modification (PTM) of proteins has a crucial role in the regulation of important cellular processes. This protocol describes the chemical synthesis of functional SUMO-peptide conjugates. The two crucial stages of this protocol are the solid-phase synthesis of peptide segments derivatized by thioester or bis(2-sulfanylethyl) amido (SEA) latent thioester functionalities and the one-pot assembly of the SUMO-peptide conjugate by a sequential native chemical ligation (NCL)/SEA native peptide ligation reaction sequence. This protocol also enables the isolation of a SUMO SEA latent thioester, which can be attached to a target peptide or protein in a subsequent step. It is compatible with 9-fluorenylmethoxycarbonyl (Fmoc) chemistry, and it gives access to homogeneous, reversible and functional SUMO conjugates that are not easily produced using living systems. The synthesis of SUMO-peptide conjugates on a milligram scale takes 20 working days.
引用
收藏
页码:269 / 292
页数:24
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