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Estimating the Stoichiometry of HIV Neutralization

HIV-1 virions infect target cells by first establishing contact between envelope glycoprotein trimers on the virion's surface and CD4 receptors on a target cell, recruiting co-receptors, fusing with the cell membrane and finally releasing the genetic material into the target cell. Specific expe...

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Detalles Bibliográficos
Autores principales: Magnus, Carsten, Regoes, Roland R.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2841622/
https://www.ncbi.nlm.nih.gov/pubmed/20333245
http://dx.doi.org/10.1371/journal.pcbi.1000713
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author Magnus, Carsten
Regoes, Roland R.
author_facet Magnus, Carsten
Regoes, Roland R.
author_sort Magnus, Carsten
collection PubMed
description HIV-1 virions infect target cells by first establishing contact between envelope glycoprotein trimers on the virion's surface and CD4 receptors on a target cell, recruiting co-receptors, fusing with the cell membrane and finally releasing the genetic material into the target cell. Specific experimental setups allow the study of the number of trimer-receptor-interactions needed for infection, i.e., the stoichiometry of entry and also the number of antibodies needed to prevent one trimer from engaging successfully in the entry process, i.e., the stoichiometry of (trimer) neutralization. Mathematical models are required to infer the stoichiometric parameters from these experimental data. Recently, we developed mathematical models for the estimations of the stoichiometry of entry [1]. In this article, we show how our models can be extended to investigate the stoichiometry of trimer neutralization. We study how various biological parameters affect the estimate of the stoichiometry of neutralization. We find that the distribution of trimer numbers—which is also an important determinant of the stoichiometry of entry—influences the estimated value of the stoichiometry of neutralization. In contrast, other parameters, which characterize the experimental system, diminish the information we can extract from the data about the stoichiometry of neutralization, and thus reduce our confidence in the estimate. We illustrate the use of our models by re-analyzing previously published data on the neutralization sensitivity [2], which contains measurements of neutralization sensitivity of viruses with different envelope proteins to antibodies with various specificities. Our mathematical framework represents the formal basis for the estimation of the stoichiometry of neutralization. Together with the stoichiometry of entry, the stoichiometry of trimer neutralization will allow one to calculate how many antibodies are required to neutralize a virion or even an entire population of virions.
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spelling pubmed-28416222010-03-24 Estimating the Stoichiometry of HIV Neutralization Magnus, Carsten Regoes, Roland R. PLoS Comput Biol Research Article HIV-1 virions infect target cells by first establishing contact between envelope glycoprotein trimers on the virion's surface and CD4 receptors on a target cell, recruiting co-receptors, fusing with the cell membrane and finally releasing the genetic material into the target cell. Specific experimental setups allow the study of the number of trimer-receptor-interactions needed for infection, i.e., the stoichiometry of entry and also the number of antibodies needed to prevent one trimer from engaging successfully in the entry process, i.e., the stoichiometry of (trimer) neutralization. Mathematical models are required to infer the stoichiometric parameters from these experimental data. Recently, we developed mathematical models for the estimations of the stoichiometry of entry [1]. In this article, we show how our models can be extended to investigate the stoichiometry of trimer neutralization. We study how various biological parameters affect the estimate of the stoichiometry of neutralization. We find that the distribution of trimer numbers—which is also an important determinant of the stoichiometry of entry—influences the estimated value of the stoichiometry of neutralization. In contrast, other parameters, which characterize the experimental system, diminish the information we can extract from the data about the stoichiometry of neutralization, and thus reduce our confidence in the estimate. We illustrate the use of our models by re-analyzing previously published data on the neutralization sensitivity [2], which contains measurements of neutralization sensitivity of viruses with different envelope proteins to antibodies with various specificities. Our mathematical framework represents the formal basis for the estimation of the stoichiometry of neutralization. Together with the stoichiometry of entry, the stoichiometry of trimer neutralization will allow one to calculate how many antibodies are required to neutralize a virion or even an entire population of virions. Public Library of Science 2010-03-19 /pmc/articles/PMC2841622/ /pubmed/20333245 http://dx.doi.org/10.1371/journal.pcbi.1000713 Text en Magnus, Regoes. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Magnus, Carsten
Regoes, Roland R.
Estimating the Stoichiometry of HIV Neutralization
title Estimating the Stoichiometry of HIV Neutralization
title_full Estimating the Stoichiometry of HIV Neutralization
title_fullStr Estimating the Stoichiometry of HIV Neutralization
title_full_unstemmed Estimating the Stoichiometry of HIV Neutralization
title_short Estimating the Stoichiometry of HIV Neutralization
title_sort estimating the stoichiometry of hiv neutralization
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2841622/
https://www.ncbi.nlm.nih.gov/pubmed/20333245
http://dx.doi.org/10.1371/journal.pcbi.1000713
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