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Synthetic peptide vaccine design: synthesis and properties of a high-density multiple antigenic peptide system.

机译:合成肽疫苗设计:高密度多抗原肽系统的合成和特性。

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摘要

A convenient and versatile approach to the direct synthesis of a peptide-antigen matrix by the solid-phase method is described. The approach is called the multiple antigen peptide system (MAP) and it utilizes a simple scaffolding of a low number of sequential levels (n) of a trifunctional amino acid as the core matrix and 2n peptide antigens to form a macromolecule with a high density of peptide antigens of final Mr 10,000. The MAP model chosen for study was an octa-branching MAP consisting of a core matrix made up of three levels of lysine and eight amino terminals for anchoring peptide antigens. The MAP, containing both the core matrix and peptides of 9-16 amino acids, was prepared in a single synthesis by the solid-phase method. Six different MAPs elicited specific antibodies in rabbits and mice, of which five produced antibodies that reacted with their corresponding native proteins. In rabbits, the sera had a considerably higher titer of antibodies than sera prepared from the same peptides anchored covalently to keyhole limpet hemocyanin as carrier. Thus, the MAP provided a general, but chemically unambiguous, approach for the preparation of carrier-bound antigens of predetermined and reproducible structure and might be suitable for generating vaccines.
机译:描述了通过固相方法直接合成肽-抗原基质的方便且通用的方法。该方法称为多抗原肽系统(MAP),它利用少量的三序氨基酸连续序列(n)作为核心基质和2n肽抗原的简单支架,形成高密度的大分子。最终Mr 10,000的肽抗原。选择用于研究的MAP模型是八分支MAP,其由核心基质组成,该核心基质由三个水平的赖氨酸和八个用于固定肽抗原的氨基末端组成。通过固相法在一次合成中制备了同时包含核心基质和9-16个氨基酸的肽的MAP。六种不同的MAP在兔和小鼠中引发了特异性抗体,其中五种产生了与相应的天然蛋白反应的抗体。在兔中,该血清具有比由共价锚定在匙孔血蓝蛋白作为载体的相同肽制备的血清更高的抗体效价。因此,MAP为制备具有预定和可再现结构的载体结合的抗原提供了通用但化学上明确的方法,并且可能适合于产生疫苗。

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