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来自AVPpred数据库的抗病毒肽的极性分布图。

Polar profile of antiviral peptides from AVPpred Database.

作者信息

Polanco Carlos, Samaniego José Lino, Castañón-González Jorge Alberto, Buhse Thomas

机构信息

Facultad de Ciencias de la Salud, Universidad Anáhuac, Av. Universidad Anáhuac No. 46, Col. Lomas Anáhuac, 52786, Huixquilucan, Estado de México, Mexico,

出版信息

Cell Biochem Biophys. 2014 Nov;70(2):1469-77. doi: 10.1007/s12013-014-0084-4.

Abstract

Diseases of viral origin in humans are among the most serious threats to health and the global economy. As recent history has shown the virus has a high pandemic potential, among other reasons, due to its ability to spread by air, hence the identification, investigation, containment, and treatment of viral diseases should be considered of paramount importance. In this sense, the bioinformatics research has focused on finding fast and efficient algorithms that can identify highly toxic antiviral peptides and to serve as a first filter, so that trials in the laboratory are substantially reduced. The work presented here contributes to this effort through the use of an algorithm already published by this team, called polarity index method, which identifies with high efficiency antiviral peptides from the exhaustive analysis of the polar profile, using the linear sequence of the peptide. The test carried out included all peptides in APD2 Database and 60 antiviral peptides identified by Kumar and co-workers (Nucleic Acids Res 40:W199-204, 2012), to build its AVPpred algorithm. The validity of the method was focused on its discriminating capacity so we included the 15 sub-classifications of both Databases.

摘要

人类的病毒性疾病是对健康和全球经济最严重的威胁之一。正如近期历史所显示的,病毒具有很高的大流行潜力,其中一个原因是它能够通过空气传播,因此,病毒性疾病的识别、调查、控制和治疗应被视为至关重要。从这个意义上说,生物信息学研究集中在寻找快速有效的算法,这些算法能够识别高毒性的抗病毒肽,并作为第一道筛选工具,从而大幅减少实验室试验。本文介绍的工作通过使用该团队已经发表的一种算法(称为极性指数法)为这一努力做出了贡献,该算法通过对肽的线性序列进行极性分布的详尽分析,高效识别抗病毒肽。所进行的测试包括APD2数据库中的所有肽以及Kumar及其同事(《核酸研究》40:W199 - 204, 2012)鉴定的60种抗病毒肽,以构建其AVPpred算法。该方法的有效性集中在其区分能力上,因此我们纳入了两个数据库的15个亚分类。

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