Lerner R A, Green N, Alexander H, Liu F T, Sutcliffe J G, Shinnick T M
Proc Natl Acad Sci U S A. 1981 Jun;78(6):3403-7. doi: 10.1073/pnas.78.6.3403.
Thirteen peptides corresponding to amino acid sequences predicted from the nucleotide sequence of the hepatitis B surface antigen were synthesized chemically. The free or carrier-linked synthetic peptides were injected into rabbits, and 7 of the 13 elicited an antipeptide response. Antisera against four of the six soluble peptides longer than 10 amino acids were reactive with native antigen and specifically precipitated the 23,000- and 28,000-dalton forms from Dane particles. As the hepatitis molecule had not been chosen for study because of any structural feature suggesting unique opportunities for success, these results suggest that the strategy is general and should work for any protein as long as enough domains are studied. Peptides such as these could prove to be ideal vaccines.
化学合成了13种与根据乙型肝炎表面抗原核苷酸序列预测的氨基酸序列相对应的肽。将游离的或与载体相连的合成肽注射到兔子体内,13种中有7种引发了抗肽反应。针对六种长度超过10个氨基酸的可溶性肽中的四种所产生的抗血清与天然抗原发生反应,并从丹氏颗粒中特异性沉淀出23000道尔顿和28000道尔顿的形式。由于选择研究的肝炎分子并非因其任何结构特征暗示有独特的成功机会,这些结果表明该策略具有普遍性,只要研究足够多的结构域,对任何蛋白质都应有效。像这样的肽可能被证明是理想的疫苗。