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用于皮下免疫的环状肽缀合物疫苗和物理混合环状肽疫苗。

Cyclic Peptide Conjugate Vaccines and Physically Mixed Cyclic Peptide Vaccines for Subcutaneous Immunization.

机构信息

School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, QLD, Australia.

Institute for Molecular Bioscience, The University of Queensland, Brisbane, QLD, Australia.

出版信息

Methods Mol Biol. 2024;2821:111-127. doi: 10.1007/978-1-0716-3914-6_9.

Abstract

Immune stimulants (adjuvants) enhance immune system recognition to provide an effective and individualized immune response when delivered with an antigen. Synthetic cyclic deca-peptides, co-administered with a toll-like receptor targeting lipopeptide, have shown self-adjuvant properties, dramatically boosting the immune response in a murine model as a subunit peptide-based vaccine containing group A Streptococcus peptide antigens.Here, we designed a novel peptide and lipid adjuvant system for the delivery of group A Streptococcus peptide antigen and a T helper peptide epitope. Following linear peptide synthesis on 2-chlorotrityl chloride resin, the linear peptide was cleaved and head-to-tail cyclized in solution. The selective arrangement of amino acids in the deca-peptide allowed for selective conjugation of lipids and/or peptide antigens following cyclisation. Using both solution-phase peptide chemistry and copper-catalyzed azide-alkyne cycloaddition reaction were covalently (and selectively) ligated lipid and/or peptide antigens onto the cyclic deca-peptide core. Subcutaneous administration of the vaccine design to mice resulted in the generation of a large number of serum immunoglobulin (Ig) G antibodies.

摘要

免疫刺激剂(佐剂)可增强免疫系统的识别能力,在与抗原一起使用时提供有效且个体化的免疫反应。与靶向 toll 样受体的脂肽联合使用的合成环状 deca-肽具有自身佐剂特性,可在小鼠模型中显著增强免疫反应,作为包含 A 组链球菌肽抗原的亚单位肽疫苗。在这里,我们设计了一种新型肽和脂质佐剂系统,用于递送 A 组链球菌肽抗原和 T 辅助肽表位。在 2-氯三苯甲基氯树脂上进行线性肽合成后,在线粒体中裂解并头尾环化。十肽中氨基酸的选择性排列允许在环化后选择性地将脂质和/或肽抗原连接到环十肽核心上。使用溶液相肽化学和铜催化的叠氮-炔环加成反应,将脂质和/或肽抗原共价(和选择性)连接到环状 deca-肽核心上。将疫苗设计皮下给药给小鼠,导致产生大量血清免疫球蛋白(IgG)抗体。

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