Kinetics of Proton Transport into Influenza Virions by the Viral M2 Channel

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Kinetics of Proton Transport into Influenza Virions by the Viral M2 Channel

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Title: Kinetics of Proton Transport into Influenza Virions by the Viral M2 Channel
Author: Rozendaal, Rutger; Popovic, Milos; van Oijen, Antoine M.; Ivanovic, Tijana; Floyd, Daniel Lee; Harrison, Stephen C.

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Citation: Ivanovic, Tijana, Rutger Rozendaal, Daniel L. Floyd, Milos Popovic, Antoine M. van Oijen, and Stephen C. Harrison. 2012. Kinetics of proton transport into influenza virions by the viral m2 channel. PLoS ONE 7(3): e31566.
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Abstract: M2 protein of influenza A viruses is a tetrameric transmembrane proton channel, which has essential functions both early and late in the virus infectious cycle. Previous studies of proton transport by M2 have been limited to measurements outside the context of the virus particle. We have developed an in vitro fluorescence-based assay to monitor internal acidification of individual virions triggered to undergo membrane fusion. We show that rimantadine, an inhibitor of M2 proton conductance, blocks the acidification-dependent dissipation of fluorescence from a pH-sensitive virus-content probe. Fusion-pore formation usually follows internal acidification but does not require it. The rate of internal virion acidification increases with external proton concentration and saturates with a \(pK_m\) of ~4.7. The rate of proton transport through a single, fully protonated M2 channel is approximately 100 to 400 protons per second. The saturating proton-concentration dependence and the low rate of internal virion acidification derived from authentic virions support a transporter model for the mechanism of proton transfer.
Published Version: doi:10.1371/journal.pone.0031566
Other Sources: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3295812/pdf/
Terms of Use: This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#LAA
Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:8796676

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