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Inhibition of cell adhesion to the virus by synthetic peptides of fiber knob of human adenovirus serotypes 2 and 3 and virus neutralisation by anti-peptide antibodies

机译:人腺病毒血清型2和3的纤维结合成肽抑制细胞对病毒的粘附以及抗肽抗体中和病毒

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摘要

The fiber knob of adenovirus (Ad) causes the first step in the interaction of adenovirus with cell membrane receptors. To obtain information on the receptor binding site(s) several synthetic peptides derived from Ad2 and Ad3 fiber head sequences and their antisera were tested for interference with virus attachment to HeLa and FL cells and cell adhesion to viruses. The anti-peptide sera were also evaluated in ELISA and virus neutralisation test. Ad2 (of subgroup C) and Ad3 (of subgroup B) attachment was not significantly inhibited by peptides corresponding to the amino acid residues 535–554, 555–573, 562–582 of Ad2 fiber or 210–225, 267–283, 291–306 and 300–319 of Ad3 fiber. However, microplate pre-adsorbed Ad3 fiber residues 210–225 and 267–283 could bind FL and HeLa cells, and 1 mg/ml of Ad3 fiber residues 267–283 inhibited the cell adhesion to Ad3 virus to approximately 90%. This peptide may participate in the receptor binding site of Ad3 fiber. ELISA reactive anti-peptide antibodies against the homologous peptide and virus did not significantly reduce the cell adhesion to the immobilised virus or the virus attachment to cells, but in the neutralisation assay antibodies raised to Ad2 fiber residues 555–573 and 562–582 and Ad3 fiber residues 210–225 caused neutralisation of the homologous virus at serum dilutions of 1:500 and 1:32, respectively. The corresponding peptides and one further peptide of Ad2 fiber and two of Ad3 fiber seem to contain neutralisation epitopes.
机译:腺病毒(Ad)的纤维结导致腺病毒与细胞膜受体相互作用的第一步。为了获得有关受体结合位点的信息,测试了几种源自Ad2和Ad3纤维头部序列的合成肽及其抗血清对病毒与HeLa和FL细胞的附着以及细胞对病毒的粘附的干扰。还通过ELISA和病毒中和试验评估了抗肽血清。与Ad2纤维的氨基酸残基535-554、555-573、562-582或210-225、267-283、291相对应的肽段并未显着抑制Ad2(C组)和Ad3(B组)的附着Ad3光纤–306和300–319。但是,微孔板预吸附的Ad3纤维残基210-225和267-283可以结合FL和HeLa细胞,并且1 mg / ml的Ad3纤维残基267-283将细胞对Ad3病毒的粘附抑制到大约90%。该肽可以参与Ad3纤维的受体结合位点。针对同源肽和病毒的ELISA反应性抗肽抗体并未显着降低细胞对固定化病毒的粘附或病毒对细胞的附着,但在中和测定中,针对Ad2纤维残基555-573和562-582和Ad3的抗体纤维残留物210–225分别在1:500和1:32的血清稀释度下导致同源病毒的中和。 Ad2纤维的相应肽和另一种肽以及Ad3纤维的两种肽似乎含有中和表位。

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