Lenstra J A, Erkens J H, Langeveld J G, Posthumus W P, Meloen R H, Gebauer F, Correa I, Enjuanes L, Stanley K K
Institute of Infectious Diseases and Immunology, Faculty of Veterinary Medicine, Utrecht, Netherlands.
J Immunol Methods. 1992 Aug 10;152(2):149-57. doi: 10.1016/0022-1759(92)90136-h.
We describe the use of random peptide sequences for the mapping of antigenic determinants. An oligonucleotide with a completely degenerate sequence of 17 or 23 nucleotides was inserted into a bacterial expression vector. This resulted in an expression library producing random hexa- or octapeptides attached to a beta-galactosidase hybrid protein. Mimotopes, or antigenic sequences that mimic an epitope, were selected by immunoscreening of colonies with monoclonal antibodies, which were specific for antigenic sites on the spike protein of the coronavirus transmissible gastroenteritis virus. We report one mimotope for antigenic site II, eight for site III and one for site IV. The site III and site IV mimotopes were closely similar to the corresponding linear epitopes, localized previously in the amino acid sequence of the S protein. An alignment of the site II mimotope and the sequence of the S protein around Trp97, which is substituted in escape mutants, suggests that this mimotope mimics a conformational epitope located around residues 97-103. Applications of mimotopes to epitope mapping, serodiagnosis and vaccine development are discussed.
我们描述了使用随机肽序列绘制抗原决定簇的方法。将一个具有17或23个核苷酸完全简并序列的寡核苷酸插入细菌表达载体中。这产生了一个表达文库,该文库产生与β-半乳糖苷酶杂合蛋白相连的随机六肽或八肽。通过用针对传染性胃肠炎冠状病毒刺突蛋白抗原位点的单克隆抗体对菌落进行免疫筛选,选择模拟表位或模拟抗原表位的抗原序列。我们报告了一个针对抗原位点II的模拟表位、八个针对位点III的模拟表位和一个针对位点IV的模拟表位。位点III和位点IV的模拟表位与先前定位在S蛋白氨基酸序列中的相应线性表位非常相似。位点II模拟表位与S蛋白在Trp97周围的序列比对(Trp97在逃逸突变体中被取代)表明,该模拟表位模拟了位于97-103位残基周围的构象表位。文中讨论了模拟表位在表位定位、血清学诊断和疫苗开发中的应用。