Literature DB >> 21738944

How many trimers? Modeling influenza virus fusion yields a minimum aggregate size of six trimers, three of which are fusogenic.

Maria Pamela Dobay1, Akos Dobay, Johnrob Bantang, Eduardo Mendoza.   

Abstract

Conflicting reports in leading journals have indicated the minimum number of influenza hemagglutinin (HA) trimers required for fusion to be between one and eight. Interestingly, the data in these reports are either almost identical, or can be transformed to be directly comparable. Different statistical or phenomenological models, however, were used to analyze these data, resulting in the varied interpretations. In an attempt to resolve this contradiction, we use PABM, a brane calculus we recently introduced, enabling an algorithmic systems biology approach that allows the problem to be modeled in a manner following a biological logic. Since a scalable PABM executor is still under development, we sufficiently simplified the fusion model and analyzed it using the model checker, PRISM. We validated the model against older HA-expressing cell-to-cell fusion data using the same parameters with the exception of three, namely HA and sialic acid (SA) surface densities and the aggregation rate, which were expected to be different as a result of the difference in the experimental setup. Results are consistent with the interpretation that a minimum aggregate size of six HA trimers, of which three undergo a conformational change to become fusogenic, is required for fusion. Of these three, two are free, while one is bound. Finally, we determined the effects of varying the SA surface density and showed that only a limited range of densities permit fusion. Our results demonstrate the potential of modeling in providing more precise interpretations of data.

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Year:  2011        PMID: 21738944     DOI: 10.1039/c1mb05060e

Source DB:  PubMed          Journal:  Mol Biosyst        ISSN: 1742-2051


  7 in total

1.  Stochastic fusion simulations and experiments suggest passive and active roles of hemagglutinin during membrane fusion.

Authors:  Donald W Lee; Vikram Thapar; Paulette Clancy; Susan Daniel
Journal:  Biophys J       Date:  2014-02-18       Impact factor: 4.033

2.  Influenza virus-membrane fusion triggered by proton uncaging for single particle studies of fusion kinetics.

Authors:  Deirdre A Costello; Donald W Lee; Jennifer Drewes; Kevin A Vasquez; Kassandra Kisler; Ulrich Wiesner; Lois Pollack; Gary R Whittaker; Susan Daniel
Journal:  Anal Chem       Date:  2012-10-01       Impact factor: 6.986

3.  Heterosubtypic antibodies to influenza A virus have limited activity against cell-bound virus but are not impaired by strain-specific serum antibodies.

Authors:  Arkadiusz Wyrzucki; Matteo Bianchi; Ines Kohler; Marco Steck; Lars Hangartner
Journal:  J Virol       Date:  2014-12-31       Impact factor: 5.103

Review 4.  Comparison of Cell Fusions Induced by Influenza Virus and SARS-CoV-2.

Authors:  Chuyuan Zhang; Xinjie Meng; Hanjun Zhao
Journal:  Int J Mol Sci       Date:  2022-07-01       Impact factor: 6.208

Review 5.  RNA structure interactions and ribonucleoprotein processes of the influenza A virus.

Authors:  Wayne K Dawson; Michal Lazniewski; Dariusz Plewczynski
Journal:  Brief Funct Genomics       Date:  2018-11-26       Impact factor: 4.241

Review 6.  Influenza virus-mediated membrane fusion: determinants of hemagglutinin fusogenic activity and experimental approaches for assessing virus fusion.

Authors:  Brian S Hamilton; Gary R Whittaker; Susan Daniel
Journal:  Viruses       Date:  2012-07-24       Impact factor: 5.048

7.  Computation of Hemagglutinin Free Energy Difference by the Confinement Method.

Authors:  Sander Boonstra; Patrick R Onck; Erik van der Giessen
Journal:  J Phys Chem B       Date:  2017-12-06       Impact factor: 2.991

  7 in total

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