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Membrane lysis during biological membrane fusion: collateral damage by misregulated fusion machines
In the canonical model of membrane fusion, the integrity of the fusing membranes is never compromised, preserving the identity of fusing compartments. However, recent molecular simulations provided evidence for a pathway to fusion in which holes in the membrane evolve into a fusion pore. Additionall...
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2568015/ https://www.ncbi.nlm.nih.gov/pubmed/18852300 http://dx.doi.org/10.1083/jcb.200805182 |
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author | Engel, Alex Walter, Peter |
author_facet | Engel, Alex Walter, Peter |
author_sort | Engel, Alex |
collection | PubMed |
description | In the canonical model of membrane fusion, the integrity of the fusing membranes is never compromised, preserving the identity of fusing compartments. However, recent molecular simulations provided evidence for a pathway to fusion in which holes in the membrane evolve into a fusion pore. Additionally, two biological membrane fusion models—yeast cell mating and in vitro vacuole fusion—have shown that modifying the composition or altering the relative expression levels of membrane fusion complexes can result in membrane lysis. The convergence of these findings showing membrane integrity loss during biological membrane fusion suggests new mechanistic models for membrane fusion and the role of membrane fusion complexes. |
format | Text |
id | pubmed-2568015 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-25680152009-04-20 Membrane lysis during biological membrane fusion: collateral damage by misregulated fusion machines Engel, Alex Walter, Peter J Cell Biol Reviews In the canonical model of membrane fusion, the integrity of the fusing membranes is never compromised, preserving the identity of fusing compartments. However, recent molecular simulations provided evidence for a pathway to fusion in which holes in the membrane evolve into a fusion pore. Additionally, two biological membrane fusion models—yeast cell mating and in vitro vacuole fusion—have shown that modifying the composition or altering the relative expression levels of membrane fusion complexes can result in membrane lysis. The convergence of these findings showing membrane integrity loss during biological membrane fusion suggests new mechanistic models for membrane fusion and the role of membrane fusion complexes. The Rockefeller University Press 2008-10-20 /pmc/articles/PMC2568015/ /pubmed/18852300 http://dx.doi.org/10.1083/jcb.200805182 Text en © 2008 Engel and Walter This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.jcb.org/misc/terms.shtml). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Reviews Engel, Alex Walter, Peter Membrane lysis during biological membrane fusion: collateral damage by misregulated fusion machines |
title | Membrane lysis during biological membrane fusion: collateral damage by misregulated fusion machines |
title_full | Membrane lysis during biological membrane fusion: collateral damage by misregulated fusion machines |
title_fullStr | Membrane lysis during biological membrane fusion: collateral damage by misregulated fusion machines |
title_full_unstemmed | Membrane lysis during biological membrane fusion: collateral damage by misregulated fusion machines |
title_short | Membrane lysis during biological membrane fusion: collateral damage by misregulated fusion machines |
title_sort | membrane lysis during biological membrane fusion: collateral damage by misregulated fusion machines |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2568015/ https://www.ncbi.nlm.nih.gov/pubmed/18852300 http://dx.doi.org/10.1083/jcb.200805182 |
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