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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.
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页码:1626 / 1634
页数:9
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