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使用SSSCPreds预测具有氨基酸突变的H5N1甲型禽流感病毒血凝素的构象变异性

Conformational Variability Prediction of H5N1 Avian Influenza A Virus Hemagglutinins with Amino Acid Mutations Using SSSCPreds.

作者信息

Izumi Hiroshi, Nafie Laurence A, Dukor Rina K

机构信息

National Institute of Advanced Industrial Science and Technology (AIST), AIST Tsukuba West Tsukuba, Ibaraki 305-8569, Japan.

Department of Chemistry, Syracuse University, Syracuse, New York 13244-4100, United States.

出版信息

ACS Omega. 2025 Aug 25;10(35):40416-40421. doi: 10.1021/acsomega.5c05850. eCollection 2025 Sep 9.

DOI:10.1021/acsomega.5c05850
PMID:40949225
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12423806/
Abstract

The worldwide outbreak of the highly pathogenic avian influenza (HPAI) H5N1 virus has sent egg prices soaring. Concomitantly, bovine and human infections of H5N1 viruses have also been observed, but there is no known person-to-person spread. The shape of the motifs is important for receptor recognition of viruses and is contradictorily deformed with amino acid mutations to avoid immunity. The deep neural network-based conformational variability prediction system of protein structures (SSSCPreds) suggests that the outbreak of HPAI is occurring in the avian world, just as the outbreak of SARS-CoV-2 was seen in the human world. The predicted flexible motif with the mutations N236K/Q238L of the B3.13 virus rationally explained the difference of specificity switching by the mutations between B3.13 and wild-type viruses, and the B-factor values were consistent with the prediction by SSSCPreds. Although the difference of only three common amino acid mutations T211I, V226A, and R341K near the sialic acid-dependent pathway and the furin cleavage sites exists between B3.13 and D1.1 viruses, the mutations of Q338L/R341K, which show the predicted rigid map pattern of the C-terminus, are one of the remarkable factors for the large difference of the case numbers for the bovine and human infections between B3.13 and D1.1 viruses.

摘要

高致病性禽流感(HPAI)H5N1病毒在全球范围内的爆发导致鸡蛋价格飙升。与此同时,也观察到了H5N1病毒感染牛和人的情况,但尚无已知的人际传播。基序的形状对于病毒的受体识别很重要,并且会因氨基酸突变而发生矛盾的变形以逃避免疫。基于深度神经网络的蛋白质结构构象变异性预测系统(SSSCPreds)表明,HPAI的爆发正在禽类世界中发生,就像SARS-CoV-2的爆发在人类世界中出现一样。B3.13病毒具有N236K/Q238L突变的预测柔性基序合理地解释了B3.13病毒与野生型病毒之间突变导致的特异性转换差异,并且B因子值与SSSCPreds的预测一致。尽管B3.13病毒和D1.1病毒在唾液酸依赖性途径和弗林蛋白酶切割位点附近仅存在三个常见氨基酸突变T211I、V226A和R341K的差异,但显示出C末端预测刚性图谱模式的Q338L/R341K突变是B3.13病毒和D1.1病毒在牛和人感染病例数上存在巨大差异的显著因素之一。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c7e2/12423806/f94c0b362378/ao5c05850_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c7e2/12423806/08374f420b89/ao5c05850_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c7e2/12423806/f6619512e520/ao5c05850_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c7e2/12423806/f94c0b362378/ao5c05850_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c7e2/12423806/08374f420b89/ao5c05850_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c7e2/12423806/f6619512e520/ao5c05850_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c7e2/12423806/f94c0b362378/ao5c05850_0003.jpg

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