甲型流感病毒非结构蛋白1家族进化过程的建模

Shaomin Yan, Guang Wu
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引用次数: 1

摘要

进化过程是一个指标如何随时间变化的数学过程,比如大脑重量随时间变化。因此,这可以在x-y坐标中表示,我们可以使用数学和统计方法来建立与时间相关的关系。在数学方法中,质量平衡式的微分方程是最有用的,因为我们可以用它来预测未来的进化指标。我们对A型流感病毒蛋白质的进化特别感兴趣,不仅因为A型流感病毒在人类和动物中引起流感,而且A型流感病毒的蛋白质在病毒中有最长的记录。在甲型流感病毒的10种蛋白质中,非结构蛋白1 (NS1)受到的关注比其他蛋白质少得多。然而,这种无知并不能降低其重要性,因为在NS1中发现了越来越多的功能。这需要将蛋白质转换为数字刻度,因为y轴更适合设置定量刻度,而不是定性刻度。在540多种将氨基酸转换为数字的方法中,我们开发了氨基酸对可预测性来完成这项工作。本文从7826个甲型流感病毒全长NS1蛋白中筛选出2729个甲型流感病毒NS1蛋白,以消除相同的序列。(1)利用氨基酸对可预测性将其转换为数字格式。(2)根据在x轴上的采样时间,我们在y轴上展示了这些蛋白质。(3)我们确定了向上和向下的半衰期作为质量平衡型微分方程解析解的初始估计。(4)利用分析溶液拟合NS1蛋白家族的进化进程。我们测试了配合度,以验证配件的正确性。这一结果证明了此类研究的积极可能性,并为未来模拟和预测蛋白质的进化过程铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Modeling of Evolutionary Progress of Nonstructure Protein 1 Family from Influenza A Virus
The evolutionary progress is mathematically how an indicator changes over time such as the brain weight changes over time. Thus, this can present in x-y coordinates, on where we can use mathematical and statistical methods to build the time-dependent relationships. Of mathematical methods, the mass-balance styled differential equation is most useful because we can use it to predict an evolutionary indicator in the future. We are particularly interested in the evolution of proteins from influenza A virus not only because influenza A virus causes influenza in humans and animals but also the proteins from influenza A virus have the longest records among viruses. Of 10 proteins from influenza A virus, the nonstructural protein 1 (NS1) gets much less attention than others. However, this ignorance does not minimize its importance because more and more functions have been found in NS1.This requires converting a protein into a numeric scale because the y-axis is better to set in a quantitative scale rather than a qualitative scale. Of 540-plus methods to convert amino acids into digital numbers, we developed the amino-acid pair predictability to do the job. In this communication, 2729 NS1 proteins of influenza A viruses filtered from 7826 full-length NS1 proteins of influenza A virus to eliminate identical sequences were employed. (1) We converted them into numeric format using the amino-acid pair predictability. (2) We presented these proteins in the y-axis according to their sampling time over the x-axis. (3) We determined upward and downward half-life as initial estimates for the analytical solution of mass-balance styled differential equations. (4) We used the analytical solution to fit the evolutionary progress of NS1 protein family. (5) We tested the goodness-of-fit to verify the fittings. The results demonstrated the positive possibility of such studies, and paved the pathway to simulate and predict the evolutionary progress of proteins in the future.
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