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Membrane Potential Depolarization as a Triggering Mechanism for Vpu-Mediated HIV-1 Release

Vpu, a component unique to HIV-1, greatly enhances the efficiency of viral particle release by unclear mechanisms. This Vpu function is intrinsically linked to its channel-like structure, which enables it to interfere with homologous transmembrane structures in infected cells. Because Vpu interacts...

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Detalles Bibliográficos
Autores principales: Hsu, Kate, Han, Jin, Shinlapawittayatorn, Krekwit, Deschenes, Isabelle, Marbán, Eduardo
Formato: Texto
Lenguaje:English
Publicado: The Biophysical Society 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2941015/
https://www.ncbi.nlm.nih.gov/pubmed/20858415
http://dx.doi.org/10.1016/j.bpj.2010.07.027
Descripción
Sumario:Vpu, a component unique to HIV-1, greatly enhances the efficiency of viral particle release by unclear mechanisms. This Vpu function is intrinsically linked to its channel-like structure, which enables it to interfere with homologous transmembrane structures in infected cells. Because Vpu interacts destructively with host background K(+) channels that set the cell resting potential, we hypothesized that Vpu might trigger viral release by destabilizing the electric field across a budding membrane. Here, we found that the efficiency of Vpu-mediated viral release is inversely correlated with membrane potential polarization. By inhibiting the background K(+) currents, Vpu dissipates the voltage constraint on viral particle discharge. As a proof of concept, we show that HIV-1 release can be accelerated by externally imposed depolarization alone. Our findings identify the trigger of Vpu-mediated release as a manifestation of the general principle of depolarization-stimulated exocytosis.