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Hepatitis C Virus p7 Induces Membrane Permeabilization by Interacting with Phosphatidylserine

Hepatitis C virus (HCV) p7 is known to be a nonselective cation channel for HCV maturation. Because the interaction of HCV proteins with host lipids in the endoplasmic reticulum membrane is crucial for the budding process, the identification of p7–lipid interactions could be important for understand...

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Autores principales: Lee, Hye-Ra, Lee, Gi Young, You, Deok-Gyun, Kim, Hong Kyu, Yoo, Young Do
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7037181/
https://www.ncbi.nlm.nih.gov/pubmed/32019133
http://dx.doi.org/10.3390/ijms21030897
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author Lee, Hye-Ra
Lee, Gi Young
You, Deok-Gyun
Kim, Hong Kyu
Yoo, Young Do
author_facet Lee, Hye-Ra
Lee, Gi Young
You, Deok-Gyun
Kim, Hong Kyu
Yoo, Young Do
author_sort Lee, Hye-Ra
collection PubMed
description Hepatitis C virus (HCV) p7 is known to be a nonselective cation channel for HCV maturation. Because the interaction of HCV proteins with host lipids in the endoplasmic reticulum membrane is crucial for the budding process, the identification of p7–lipid interactions could be important for understanding the HCV life cycle. Here, we report that p7 interacts with phosphatidylserine (PS) to induce membrane permeabilization. The interaction of p7 with PS was not inhibited by Gd(3+) ions, which have been known to interact with negatively charged lipids, but channel activity and p7-induced mitochondrial depolarization were inhibited by Gd(3+) ions. From the present results, we suggest that the p7–PS interaction plays an essential role in regulating its ion channel function and could be a potential molecular target for anti-HCV therapy.
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spelling pubmed-70371812020-03-11 Hepatitis C Virus p7 Induces Membrane Permeabilization by Interacting with Phosphatidylserine Lee, Hye-Ra Lee, Gi Young You, Deok-Gyun Kim, Hong Kyu Yoo, Young Do Int J Mol Sci Article Hepatitis C virus (HCV) p7 is known to be a nonselective cation channel for HCV maturation. Because the interaction of HCV proteins with host lipids in the endoplasmic reticulum membrane is crucial for the budding process, the identification of p7–lipid interactions could be important for understanding the HCV life cycle. Here, we report that p7 interacts with phosphatidylserine (PS) to induce membrane permeabilization. The interaction of p7 with PS was not inhibited by Gd(3+) ions, which have been known to interact with negatively charged lipids, but channel activity and p7-induced mitochondrial depolarization were inhibited by Gd(3+) ions. From the present results, we suggest that the p7–PS interaction plays an essential role in regulating its ion channel function and could be a potential molecular target for anti-HCV therapy. MDPI 2020-01-30 /pmc/articles/PMC7037181/ /pubmed/32019133 http://dx.doi.org/10.3390/ijms21030897 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lee, Hye-Ra
Lee, Gi Young
You, Deok-Gyun
Kim, Hong Kyu
Yoo, Young Do
Hepatitis C Virus p7 Induces Membrane Permeabilization by Interacting with Phosphatidylserine
title Hepatitis C Virus p7 Induces Membrane Permeabilization by Interacting with Phosphatidylserine
title_full Hepatitis C Virus p7 Induces Membrane Permeabilization by Interacting with Phosphatidylserine
title_fullStr Hepatitis C Virus p7 Induces Membrane Permeabilization by Interacting with Phosphatidylserine
title_full_unstemmed Hepatitis C Virus p7 Induces Membrane Permeabilization by Interacting with Phosphatidylserine
title_short Hepatitis C Virus p7 Induces Membrane Permeabilization by Interacting with Phosphatidylserine
title_sort hepatitis c virus p7 induces membrane permeabilization by interacting with phosphatidylserine
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7037181/
https://www.ncbi.nlm.nih.gov/pubmed/32019133
http://dx.doi.org/10.3390/ijms21030897
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