A strategy for rapidly making a vaccine and treatment for the disease caused by the Wuhan-Corona Virus 2019 (COVID19)-Part two

G. Pieczenik
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引用次数: 1

Abstract

Presently, a majority of bioinformaticians analyze sequences by homology between the amino acid sequences of proteins. The assumption in this type of analysis is that if an identical nucleotide sequence codes for an identical peptide sequence in two different proteins in two different viruses; then, this is evidence of “descent from a common ancestor”. This is the Darwinian assumption and is the most common method of analysis. Just recently, for example, the following sequence VLLFLAFVV was identified as a common epitope in the Envelope protein (E) of both SARS and COVID19 [3] and they suggest this as the epitope for the basis of a vaccine. Their work is quite pretty. However, we feel that this may not be the best epitope on which to base a vaccine. We have two reasons. Firstly, this sequence is completely hydrophobic and that is rare in antibody-epitope interactions.
2019年武汉冠状病毒(covid - 19)引起的疾病的快速疫苗和治疗战略-第二部分
目前,大多数生物信息学家通过蛋白质氨基酸序列之间的同源性来分析序列。这种分析的假设是,如果相同的核苷酸序列在两种不同病毒的两种不同蛋白质中编码相同的肽序列;那么,这就是“共同祖先的后裔”的证据。这是达尔文的假设,也是最常用的分析方法。例如,就在最近,以下序列VLLFLAFVV被鉴定为SARS和covid - 19[3]的包膜蛋白(E)中的共同表位,他们建议将其作为疫苗基础的表位。他们的工作相当漂亮。然而,我们认为这可能不是建立疫苗基础的最佳表位。我们有两个理由。首先,这个序列是完全疏水的,这在抗体-表位相互作用中是罕见的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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