School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, QLD, Australia.
Institute for Molecular Bioscience, The University of Queensland, Brisbane, QLD, Australia.
Methods Mol Biol. 2024;2821:111-127. doi: 10.1007/978-1-0716-3914-6_9.
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.
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。