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对15种腺病毒六邻体蛋白的分析揭示了七个含有血清型特异性残基的高变区的位置和结构。

Analysis of 15 adenovirus hexon proteins reveals the location and structure of seven hypervariable regions containing serotype-specific residues.

作者信息

Crawford-Miksza L, Schnurr D P

机构信息

Viral and Rickettsial Disease Laboratory, California Department of Health Services Berkeley 94704, USA.

出版信息

J Virol. 1996 Mar;70(3):1836-44. doi: 10.1128/JVI.70.3.1836-1844.1996.

Abstract

The first full-length hexon protein DNA and deduced amino acid sequences of a subgenus D adenovirus (AV) were determined from candidate AV48 (85-0844). Comprehensive comparison of this sequence with hexon protein sequences from human subgenera A, B, C, D, F, bovine AV3, and mouse AV1 revealed seven discrete hypervariable regions (HVRs) among the 250 variable residues in loops 1 and 2. These regions differed in length between serotypes, from 2 to 38 residues, and contained > 00% of hexon serotype-specific residues among human serotypes. Alignment with the published crystal structure of AV2 established the location and structure of the type-specific regions. Five HVRs were shown to be part of linear loops on the exposed surfaces of the protein, analogous to the serotype-specific loops or "puffs" in picornavirus capsid proteins. The HVRs were supported by a common framework of conserved residues, of which 68 to 75% were hydrophobic. Unique sequences were limited to the seven HVRs, so that one or more of these regions contain the type-specific neutralization epitopes. A neutralizing AV48 hexon-specific antiserum recognized linear peptides that corresponded to six HVRs by enzyme immunoassay. Affinity-purification removal of all peptide-reactive antibodies did not significantly decrease the neutralization titer. Eluted peptide-reactive antibodies did not neutralize. Human antisera that neutralized AV48 did not recognize linear peptides. Purified trimeric native hexon inhibited neutralization, but monomeric heat-denatured hexon did not. We conclude that the AV48 neutralization epitope(s) is complex and conformational.

摘要

从候选腺病毒48型(85 - 0844)中确定了D亚属腺病毒(AV)的首个全长六邻体蛋白DNA及推导的氨基酸序列。将该序列与人类A、B、C、D、F亚属、牛腺病毒3型和小鼠腺病毒1型的六邻体蛋白序列进行全面比较,发现在环1和环2的250个可变残基中有7个离散的高变区(HVRs)。这些区域在不同血清型之间长度不同,从2到38个残基不等,并且在人类血清型中包含> 00%的六邻体血清型特异性残基。与已发表的腺病毒2型晶体结构比对确定了型特异性区域的位置和结构。5个HVRs被证明是该蛋白暴露表面线性环的一部分,类似于微小核糖核酸病毒衣壳蛋白中的血清型特异性环或“隆起”。HVRs由保守残基组成的共同框架支撑,其中68%至75%是疏水的。独特序列仅限于这7个HVRs,因此这些区域中的一个或多个包含型特异性中和表位。一种中和腺病毒48型六邻体特异性抗血清通过酶免疫测定识别与6个HVRs对应的线性肽。亲和纯化去除所有肽反应性抗体并未显著降低中和效价。洗脱的肽反应性抗体没有中和作用。中和腺病毒48型的人抗血清不识别线性肽。纯化的三聚体天然六邻体抑制中和作用,但单体热变性六邻体则不然。我们得出结论,腺病毒48型中和表位是复杂的且为构象性的。

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