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Vesicular stomatitis virus G protein transmembrane region is crucial for the hemi-fusion to full fusion transition
Viral fusion proteins are essential for enveloped virus infection. These proteins mediate fusion between the virus envelope and host cellular membrane to release the viral genome into cells. Vesicular stomatitis virus G (VSV G) protein is a typical type III viral fusion protein. To study the mechani...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6045571/ https://www.ncbi.nlm.nih.gov/pubmed/30006542 http://dx.doi.org/10.1038/s41598-018-28868-y |
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author | Ci, Yali Yang, Yang Xu, Caimin Shi, Lei |
author_facet | Ci, Yali Yang, Yang Xu, Caimin Shi, Lei |
author_sort | Ci, Yali |
collection | PubMed |
description | Viral fusion proteins are essential for enveloped virus infection. These proteins mediate fusion between the virus envelope and host cellular membrane to release the viral genome into cells. Vesicular stomatitis virus G (VSV G) protein is a typical type III viral fusion protein. To study the mechanism of VSV G protein mediated membrane fusion, we set up a cell-cell fusion system in which cells are marked by different fluorescent proteins. Taking advantage of this system, we performed real-time recording and quantitative analysis of the cell fusion mediated by VSV G. We found that the time scale required for VSV G mediated cell-cell fusion was approximately 1–2 minutes. Next, we specifically examined the function of the transmembrane (TM) region of VSV G protein in membrane fusion by replacing the TM region with those of other fusion proteins. The TM region replacements dramatically impaired VSV G protein function in the cell-cell fusion assay and diminished VSV G mediated lentivirus and recombinant VSV infection efficiency. Further experiments implied that the TM region played a role in the transition from hemi-fusion to full fusion. Several residues within the TM region were identified as important for membrane fusion. Overall, our findings unraveled the important function of the TM region in VSV G mediated viral fusion. |
format | Online Article Text |
id | pubmed-6045571 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60455712018-07-15 Vesicular stomatitis virus G protein transmembrane region is crucial for the hemi-fusion to full fusion transition Ci, Yali Yang, Yang Xu, Caimin Shi, Lei Sci Rep Article Viral fusion proteins are essential for enveloped virus infection. These proteins mediate fusion between the virus envelope and host cellular membrane to release the viral genome into cells. Vesicular stomatitis virus G (VSV G) protein is a typical type III viral fusion protein. To study the mechanism of VSV G protein mediated membrane fusion, we set up a cell-cell fusion system in which cells are marked by different fluorescent proteins. Taking advantage of this system, we performed real-time recording and quantitative analysis of the cell fusion mediated by VSV G. We found that the time scale required for VSV G mediated cell-cell fusion was approximately 1–2 minutes. Next, we specifically examined the function of the transmembrane (TM) region of VSV G protein in membrane fusion by replacing the TM region with those of other fusion proteins. The TM region replacements dramatically impaired VSV G protein function in the cell-cell fusion assay and diminished VSV G mediated lentivirus and recombinant VSV infection efficiency. Further experiments implied that the TM region played a role in the transition from hemi-fusion to full fusion. Several residues within the TM region were identified as important for membrane fusion. Overall, our findings unraveled the important function of the TM region in VSV G mediated viral fusion. Nature Publishing Group UK 2018-07-13 /pmc/articles/PMC6045571/ /pubmed/30006542 http://dx.doi.org/10.1038/s41598-018-28868-y Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Ci, Yali Yang, Yang Xu, Caimin Shi, Lei Vesicular stomatitis virus G protein transmembrane region is crucial for the hemi-fusion to full fusion transition |
title | Vesicular stomatitis virus G protein transmembrane region is crucial for the hemi-fusion to full fusion transition |
title_full | Vesicular stomatitis virus G protein transmembrane region is crucial for the hemi-fusion to full fusion transition |
title_fullStr | Vesicular stomatitis virus G protein transmembrane region is crucial for the hemi-fusion to full fusion transition |
title_full_unstemmed | Vesicular stomatitis virus G protein transmembrane region is crucial for the hemi-fusion to full fusion transition |
title_short | Vesicular stomatitis virus G protein transmembrane region is crucial for the hemi-fusion to full fusion transition |
title_sort | vesicular stomatitis virus g protein transmembrane region is crucial for the hemi-fusion to full fusion transition |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6045571/ https://www.ncbi.nlm.nih.gov/pubmed/30006542 http://dx.doi.org/10.1038/s41598-018-28868-y |
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