Peptide-Based Multiepitopic Vaccine Platforms via Click Reactions

被引:13
|
作者
Forner, Mar [1 ]
Defaus, Sira [1 ]
Andreu, David [1 ]
机构
[1] Pompeu Fabra Univ, Dept Expt & Hlth Sci, Barcelona Biomed Res Pk, Barcelona 08003, Spain
来源
JOURNAL OF ORGANIC CHEMISTRY | 2020年 / 85卷 / 03期
关键词
CATALYZED ALKYNE-AZIDE; CHEMICAL-SYNTHESIS; MOUTH-DISEASE; PROTECTION; LIGATION; CYCLOADDITION; CONJUGATION; CHALLENGES; FUTURE;
D O I
10.1021/acs.joc.9b02798
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Multimeric antigen display and high overall valency are increasingly regarded as strategic goals for potent and broadly efficacious synthetic vaccines with potential market prospects. Herein, a modular and versatile approach to multifunctional peptide-based vaccine platforms at multimilligram scale in reasonable yields is reported. Preparation of chemoselectively modified peptide building blocks of medium-to-large size, conjugation of these subunits, and final assembly were achieved by a combination of Michael type thiol-ene addition and copper(I)-mediated alkyne-azide cycloaddition. The size and structural complexity of the building blocks required exploration of a further level of orthogonality, namely furan/maleimide Diels-Alder chemistry. After process optimization, a finely tuned, stepwise click approach has emerged as a workable, on-demand strategy to create macromolecular therapeutic vaccine assemblies.
引用
收藏
页码:1626 / 1634
页数:9
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