Mazurkova N A, Kalashnikov V V, Mizenko G A, Samukov V V, Podcherniaeva R Ia
Vopr Virusol. 1990 Jul-Aug;35(4):283-6.
C-terminal peptide fragments of the heavy chain (HA1) of influenza virus, subtypes H1 and H3, hemagglutinins were synthesized. Rabbits and guinea pigs immunized with peptides H3 (314-328) and H1 (314-328) conjugates with BSA developed high immune response to conjugated peptides. Solid-phase RIA demonstrated interaction of antisera to peptide H3 (314-328) with A/Aichi/2/68 virus which was inhibited by peptides H3 (314-328) and H3 (317-328) but not by H3 (320-328), that is, antibodies interacted predominantly with amino acids 317-323 HA1. Anti-H3 (314-328)-BSA showed a marked activity in H1 and NT with a number of H3 subtype viruses. Antisera to peptide H1 (314-328) reacted with A/PR/8/34 virus insignificantly and were also inactive in H1 and NT with subtype H1 viruses.
合成了甲型流感病毒H1和H3亚型血凝素重链(HA1)的C末端肽片段。用肽H3(314 - 328)和H1(314 - 328)与牛血清白蛋白(BSA)的偶联物免疫的兔子和豚鼠对偶联肽产生了高免疫反应。固相放射免疫分析表明,抗肽H3(314 - 328)的抗血清与A/爱知/2/68病毒发生相互作用,这种相互作用被肽H3(314 - 328)和H3(317 - 328)抑制,但不被H3(320 - 328)抑制,也就是说,抗体主要与HA1的317 - 323位氨基酸相互作用。抗H3(314 - 328)-BSA在对多种H3亚型病毒的血凝抑制(HI)和神经氨酸酶抑制(NT)试验中表现出显著活性。抗肽H1(314 - 328)的抗血清与A/PR/8/34病毒反应不明显,并且在对H1亚型病毒的HI和NT试验中也无活性。