分析人或伊蚊寨卡病毒E蛋白的计算机辅助疫苗设计

J. Weltman
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引用次数: 8

摘要

测定了从受感染者和伊蚊中分离的寨卡病毒(Zika)包膜E蛋白的信息熵(H)和预测B细胞表位评分(Bepipred),目的是确定可能作为抗寨卡病毒疫苗免疫靶点的E蛋白区域。蚊源E蛋白的总H值比人源E蛋白的总H值高4.2380,提示人类宿主对寨卡病毒突变有一定的限制。鉴定出长度大于等于10个氨基酸的7个不变肽(H=0.0)。筛选H=0.0的肽序列预测表位。7个不变肽由93个氨基酸残基组成,其中31个具有预测b细胞表位活性。预测的表位残基主要分布在7个不变肽中的5个上。我们提出,人类和伊蚊寨卡病毒E蛋白中的这5个不变(H=0)肽代表了具有受限突变/进化潜力的结构域,并且预测这些不变结构域中的表位可能是开发抗寨卡病毒疫苗的稳定免疫靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Computer-Assisted Vaccine Design by Analysis of Zika Virus E ProteinsObtained either from Humans or from Aedes Mosquitos
Information entropy (H) and predicted B cell epitope score (Bepipred) were determined for the envelope E protein of Zika viruses (ZIKV) isolated from infected humans and Aedes mosquitos with the aim of identifying E protein regions that may be useful as immunological targets of anti-ZIKV vaccines. Total H of mosquito origin E proteins was 4.2380 greater than that of E proteins of human origin, suggestive of constraints on ZIKV mutation in the human host. Seven invariant peptides (H=0.0) of length 10 amino acids, or greater, were identified. These peptide sequences where H=0.0 were screened for predicted epitopes. The seven invariant peptides were comprised of 93 amino acid residues, 31 of which demonstrated predicted B-cell epitopic activity. The predicted epitopic residues were distributed predominantly to 5 of the 7 invariant peptides. It is proposed that these 5 invariant (H=0) peptides in the E proteins of both human and Aedes mosquito ZIKV represent domains with constrained mutational/evolutionary potential and that epitopes predicted to reside in such invariant domains thus may be stable immunological targets for development of an anti-ZIKV vaccine.
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