tetano
Editor, Senior Moderator
Biophys J. 2015 Nov 3;109(9):1917-24. doi: 10.1016/j.bpj.2015.09.014.
[h=1]Hemagglutinin Spatial Distribution Shifts in Response to Cholesterol in the Influenza Viral Envelope.[/h] Domanska MK[SUP]1[/SUP], Dunning RA[SUP]1[/SUP], Dryden KA[SUP]1[/SUP], Zawada KE[SUP]1[/SUP], Yeager M[SUP]1[/SUP], Kasson PM[SUP]2[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] Influenza virus delivers its genome to the host cytoplasm via a process of membrane fusion mediated by the viral hemagglutinin protein. Optimal fusion likely requires multiple hemagglutinin trimers, so the spatial distribution of hemagglutinin on the viral envelope may influence fusion mechanism. We have previously shown that moderate depletion of cholesterol from the influenza viral envelope accelerates fusion kinetics even though it decreases fusion efficiency, both in a reversible manner. Here, we use electron cryo-microscopy to measure how the hemagglutinin lateral density in the viral envelope changes with cholesterol extraction. We extract this information by measuring the radial distribution function of electron density in >4000 viral images per sample, assigning hemagglutinin density by comparing images with and without anti-HA Fab bound. On average, hemagglutinin trimers move closer together: we estimate that the typical trimer-trimer spacing reduces from 94 to 84 ? when ∼90% of cholesterol is removed from the viral membrane. Upon restoration of viral envelope cholesterol, this spacing once again expands. This finding can qualitatively explain the observed changes to fusion kinetics: contemporary models from single-virus microscopy are that fusion requires the engagement of several hemagglutinin trimers in close proximity. If removing cholesterol increases the lateral density of hemagglutinin, this should result in an increase in the rate of fusion.
Copyright ? 2015 Biophysical Society. Published by Elsevier Inc. All rights reserved.
PMID: 26536268 [PubMed - in process]
[h=1]Hemagglutinin Spatial Distribution Shifts in Response to Cholesterol in the Influenza Viral Envelope.[/h] Domanska MK[SUP]1[/SUP], Dunning RA[SUP]1[/SUP], Dryden KA[SUP]1[/SUP], Zawada KE[SUP]1[/SUP], Yeager M[SUP]1[/SUP], Kasson PM[SUP]2[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] Influenza virus delivers its genome to the host cytoplasm via a process of membrane fusion mediated by the viral hemagglutinin protein. Optimal fusion likely requires multiple hemagglutinin trimers, so the spatial distribution of hemagglutinin on the viral envelope may influence fusion mechanism. We have previously shown that moderate depletion of cholesterol from the influenza viral envelope accelerates fusion kinetics even though it decreases fusion efficiency, both in a reversible manner. Here, we use electron cryo-microscopy to measure how the hemagglutinin lateral density in the viral envelope changes with cholesterol extraction. We extract this information by measuring the radial distribution function of electron density in >4000 viral images per sample, assigning hemagglutinin density by comparing images with and without anti-HA Fab bound. On average, hemagglutinin trimers move closer together: we estimate that the typical trimer-trimer spacing reduces from 94 to 84 ? when ∼90% of cholesterol is removed from the viral membrane. Upon restoration of viral envelope cholesterol, this spacing once again expands. This finding can qualitatively explain the observed changes to fusion kinetics: contemporary models from single-virus microscopy are that fusion requires the engagement of several hemagglutinin trimers in close proximity. If removing cholesterol increases the lateral density of hemagglutinin, this should result in an increase in the rate of fusion.
Copyright ? 2015 Biophysical Society. Published by Elsevier Inc. All rights reserved.
PMID: 26536268 [PubMed - in process]