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模拟每个病毒体中有多少包膜糖蛋白三聚体参与人类免疫缺陷病毒的感染性及其抗体中和作用。

Modeling how many envelope glycoprotein trimers per virion participate in human immunodeficiency virus infectivity and its neutralization by antibody.

作者信息

Klasse Per Johan

机构信息

Department of Microbiology and Immunology, Cornell University, Weill Medical College, 1300 York Avenue, Box 62, New York, NY 10021, USA.

出版信息

Virology. 2007 Dec 20;369(2):245-62. doi: 10.1016/j.virol.2007.06.044. Epub 2007 Sep 7.

Abstract

Trimers of the HIV-1 envelope glycoprotein (Env) effectuate viral entry into susceptible cells. Therefore Env trimers are the targets for neutralizing antibodies. This study models the number of trimers required for virion infectivity. It also delineates the minimum number of antibody molecules that would neutralize a virion. First, Env function was assumed to be incremental (all envelope glycoprotein units contribute equally) or liminal (characterized by thresholds). Then, such models were combined and shown to fit published data on phenotypically mixed pseudotype viruses. Virions with 9 trimers would require around a median of 5 of them for strong infectivity; the proportion varies among strains and mutants. In addition, the models account for both liminal and incremental protomeric effects at the trimer level: different inert Env mutants may affect trimer function in different degrees. Because of compensatory effects at the virion and trimer levels, however, current data cannot differentiate between all plausible models. But the biophysically and mathematically rationalized blurring of thresholds yields candidate models that fit different data excellently.

摘要

HIV-1包膜糖蛋白(Env)三聚体介导病毒进入易感细胞。因此,Env三聚体是中和抗体的作用靶点。本研究对病毒体感染性所需的三聚体数量进行了建模。它还描述了中和一个病毒体所需的抗体分子的最小数量。首先,假设Env功能是递增的(所有包膜糖蛋白单位贡献相同)或阈限性的(以阈值为特征)。然后,将这些模型结合起来,结果表明它们与已发表的关于表型混合假型病毒的数据相符。具有9个三聚体的病毒体若要具有较强的感染性,大约需要其中位数5个三聚体;不同毒株和突变体的比例有所不同。此外,这些模型考虑了三聚体水平上的阈限性和递增性原聚体效应:不同的无活性Env突变体可能对三聚体功能有不同程度的影响。然而,由于病毒体和三聚体水平上的补偿效应,目前的数据无法区分所有合理的模型。但是,从生物物理学和数学角度进行合理阐释的阈值模糊产生了能够很好拟合不同数据的候选模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9856/2317823/675b2f7d6bef/nihms35048f1a.jpg

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