Petrov V N, Rybakov S S, Petrova O N, Chepurkin A V, Gulenkin V M
National Research Institute for Animal Health, Ministry of Agriculture and Food, Russian Federation, Vladimir, Russia.
Bioorg Khim. 1998 Dec;24(12):899-905.
Potential immunodominant epitopes were predicted on the basis of a theoretical analysis of the antigenic structure of the VP1 protein of the type Asia-1 foot-and-mouth disease virus. Peptides corresponding to the 140-153, 136-153, 132-153, 143-157, 137-157, and 193-208 fragments of the VP1 protein sequence were synthesized by the solid phase method, and the immunogenic properties of the peptides were studied on guinea pigs. The shortest peptide exhibiting the protective effect was found to correspond to the, 140-153 fragment of the VP1 sequence. The Plm-(Gly)3-(140-153)-(Gly)2-Lys(Plm)-Leu and [Ac-(140-153)-(Gly)3]8-(Lys)7-Gly synthetic constructions in combination with adjuvants provided up to 80% protection of immunized animals against infection with the foot-and-mouth disease virus.
基于对亚洲1型口蹄疫病毒VP1蛋白抗原结构的理论分析,预测了潜在的免疫显性表位。通过固相法合成了与VP1蛋白序列的140 - 153、136 - 153、132 - 153、143 - 157、137 - 157和193 - 208片段相对应的肽,并在豚鼠身上研究了这些肽的免疫原性。发现表现出保护作用的最短肽对应于VP1序列的140 - 153片段。Plm-(Gly)3-(140 - 153)-(Gly)2-Lys(Plm)-Leu和[Ac-(140 - 153)-(Gly)3]8-(Lys)7-Gly合成构建体与佐剂联合使用,可为免疫动物提供高达80%的保护,使其免受口蹄疫病毒感染。