Shapira M, Jibson M, Muller G, Arnon R
Proc Natl Acad Sci U S A. 1984 Apr;81(8):2461-5. doi: 10.1073/pnas.81.8.2461.
Four peptides have been synthesized, corresponding to different regions of the H3 influenza hemagglutinin, that are related to antigenic sites "A" and "B" of the molecule. The peptides consisted of the following sequences: 139-146, which forms the "loop" in the native hemagglutinin molecule, with either glycine or aspartic acid at position 144; 147-164, which contains part of antigenic determinant "B"; and 138-164, which comprises both the loop and the area 147-164. The peptides were conjugated to tetanus toxoid and used for immunization of rabbits and mice. All four conjugates elicited an immune response against the homologous peptides, but only the peptides 138-164 and 147-164 gave rise to antibodies that recognized and bound to the intact virus. Protection of mice against challenge infection with A/Eng/42/72 virus was achieved only by immunization with the conjugate (138-164)-TT, which led to partial protective effect. These data emphasize the role of molecular structure in determining the antigenic properties of synthetic peptides and indicate that the length of the peptide could be crucial for enforcing the right folding required to mimic the native structure.
已合成了四种肽,它们对应于H3流感血凝素的不同区域,与该分子的抗原位点“A”和“B”相关。这些肽由以下序列组成:139 - 146,它在天然血凝素分子中形成“环”,在第144位为甘氨酸或天冬氨酸;147 - 164,它包含抗原决定簇“B”的一部分;以及138 - 164,它既包含环又包含147 - 164区域。将这些肽与破伤风类毒素偶联,并用于免疫兔子和小鼠。所有四种偶联物都引发了针对同源肽的免疫反应,但只有肽138 - 164和147 - 164产生了能识别并结合完整病毒的抗体。仅通过用偶联物(138 - 164)-TT免疫才能使小鼠抵御A/Eng/42/72病毒的攻击感染,这产生了部分保护作用。这些数据强调了分子结构在决定合成肽抗原特性中的作用,并表明肽的长度对于强制形成模仿天然结构所需的正确折叠可能至关重要。