Broekhuijsen M P, Blom T, van Rijn J, Pouwels P H, Klasen E A, Fasbender M J, Enger-Valk B E
Gene. 1986;49(2):189-97. doi: 10.1016/0378-1119(86)90279-9.
A series of four expression plasmids coding for fusion proteins containing foot-and-mouth disease virus (FMDV) sequences was constructed. The fusion proteins contain a large part of beta-galactosidase from Escherichia coli preceded (N-terminal) by 1, 2, 4 or 8 repeats of the antigenic determinant of FMDV consisting of amino acids 137-162 of the capsid polypeptide VP1. All four fusion proteins were efficiently produced in E. coli host bacteria. Immunization of rabbits resulted in FMDV-specific, neutralizing antibodies, the response being dependent on the number of repeats. With enzyme-linked immunosorbent-assay techniques it was shown that the FMDV antigenic determinants are exposed on the surface of the fusion proteins under non-denaturing conditions.
构建了一系列四个表达质粒,其编码含有口蹄疫病毒(FMDV)序列的融合蛋白。这些融合蛋白包含来自大肠杆菌的大部分β-半乳糖苷酶,在其之前(N端)有FMDV抗原决定簇的1、2、4或8个重复序列,该抗原决定簇由衣壳多肽VP1的氨基酸137 - 162组成。所有四种融合蛋白都在大肠杆菌宿主细菌中高效产生。用这些融合蛋白免疫兔子可产生FMDV特异性中和抗体,抗体反应取决于重复序列的数量。采用酶联免疫吸附测定技术表明,在非变性条件下,FMDV抗原决定簇暴露在融合蛋白的表面。