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快速评估流感病毒血凝素与人及禽类受体的结合活性。

Rapid estimation of binding activity of influenza virus hemagglutinin to human and avian receptors.

机构信息

National Laboratory of Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing, China.

出版信息

PLoS One. 2011 Apr 13;6(4):e18664. doi: 10.1371/journal.pone.0018664.

Abstract

A critical step for avian influenza viruses to infect human hosts and cause epidemics or pandemics is acquisition of the ability of the viral hemagglutinin (HA) to bind to human receptors. However, current global influenza surveillance does not monitor HA binding specificity due to a lack of rapid and reliable assays. Here we report a computational method that uses an effective scoring function to quantify HA-receptor binding activities with high accuracy and speed. Application of this method reveals receptor specificity changes and its temporal relationship with antigenicity changes during the evolution of human H3N2 viruses. The method predicts that two amino acid differences at 222 and 225 between HAs of A/Fujian/411/02 and A/Panama/2007/99 viruses account for their differences in binding to both avian and human receptors; this prediction was verified experimentally. The new computational method could provide an urgently needed tool for rapid and large-scale analysis of HA receptor specificities for global influenza surveillance.

摘要

禽流感病毒感染人类宿主并引发疫情或大流行的关键步骤是获得病毒血凝素(HA)结合人类受体的能力。然而,由于缺乏快速可靠的检测方法,目前的全球流感监测并未监测 HA 结合特异性。在这里,我们报告了一种计算方法,该方法使用有效的评分函数来准确快速地量化 HA-受体结合活性。该方法的应用揭示了人类 H3N2 病毒进化过程中受体特异性变化及其与抗原性变化的时间关系。该方法预测,A/Fujian/411/02 和 A/Panama/2007/99 病毒 HA 之间的 222 和 225 位的两个氨基酸差异导致了它们在结合禽源和人类受体方面的差异;该预测得到了实验验证。新的计算方法可以为快速大规模分析全球流感监测中的 HA 受体特异性提供急需的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d5/3076431/db5e70958fcd/pone.0018664.g001.jpg

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