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Real-time intermembrane force measurements and imaging of lipid domain morphology during hemifusion
Membrane fusion is the core process in membrane trafficking and is essential for cellular transport of proteins and other biomacromolecules. During protein-mediated membrane fusion, membrane proteins are often excluded from the membrane–membrane contact, indicating that local structural transformati...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4455132/ https://www.ncbi.nlm.nih.gov/pubmed/26006266 http://dx.doi.org/10.1038/ncomms8238 |
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author | Lee, Dong Woog Kristiansen, Kai Donaldson, Jr., Stephen H. Cadirov, Nicholas Banquy, Xavier Israelachvili, Jacob N. |
author_facet | Lee, Dong Woog Kristiansen, Kai Donaldson, Jr., Stephen H. Cadirov, Nicholas Banquy, Xavier Israelachvili, Jacob N. |
author_sort | Lee, Dong Woog |
collection | PubMed |
description | Membrane fusion is the core process in membrane trafficking and is essential for cellular transport of proteins and other biomacromolecules. During protein-mediated membrane fusion, membrane proteins are often excluded from the membrane–membrane contact, indicating that local structural transformations in lipid domains play a major role. However, the rearrangements of lipid domains during fusion have not been thoroughly examined. Here using a newly developed Fluorescence Surface Forces Apparatus (FL-SFA), migration of liquid-disordered clusters and depletion of liquid-ordered domains at the membrane–membrane contact are imaged in real time during hemifusion of model lipid membranes, together with simultaneous force–distance and lipid membrane thickness measurements. The load and contact time-dependent hemifusion results show that the domain rearrangements decrease the energy barrier to fusion, illustrating the significance of dynamic domain transformations in membrane fusion processes. Importantly, the FL-SFA can unambiguously correlate interaction forces and in situ imaging in many dynamic interfacial systems. |
format | Online Article Text |
id | pubmed-4455132 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-44551322015-06-18 Real-time intermembrane force measurements and imaging of lipid domain morphology during hemifusion Lee, Dong Woog Kristiansen, Kai Donaldson, Jr., Stephen H. Cadirov, Nicholas Banquy, Xavier Israelachvili, Jacob N. Nat Commun Article Membrane fusion is the core process in membrane trafficking and is essential for cellular transport of proteins and other biomacromolecules. During protein-mediated membrane fusion, membrane proteins are often excluded from the membrane–membrane contact, indicating that local structural transformations in lipid domains play a major role. However, the rearrangements of lipid domains during fusion have not been thoroughly examined. Here using a newly developed Fluorescence Surface Forces Apparatus (FL-SFA), migration of liquid-disordered clusters and depletion of liquid-ordered domains at the membrane–membrane contact are imaged in real time during hemifusion of model lipid membranes, together with simultaneous force–distance and lipid membrane thickness measurements. The load and contact time-dependent hemifusion results show that the domain rearrangements decrease the energy barrier to fusion, illustrating the significance of dynamic domain transformations in membrane fusion processes. Importantly, the FL-SFA can unambiguously correlate interaction forces and in situ imaging in many dynamic interfacial systems. Nature Pub. Group 2015-05-26 /pmc/articles/PMC4455132/ /pubmed/26006266 http://dx.doi.org/10.1038/ncomms8238 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Lee, Dong Woog Kristiansen, Kai Donaldson, Jr., Stephen H. Cadirov, Nicholas Banquy, Xavier Israelachvili, Jacob N. Real-time intermembrane force measurements and imaging of lipid domain morphology during hemifusion |
title | Real-time intermembrane force measurements and imaging of lipid domain morphology during hemifusion |
title_full | Real-time intermembrane force measurements and imaging of lipid domain morphology during hemifusion |
title_fullStr | Real-time intermembrane force measurements and imaging of lipid domain morphology during hemifusion |
title_full_unstemmed | Real-time intermembrane force measurements and imaging of lipid domain morphology during hemifusion |
title_short | Real-time intermembrane force measurements and imaging of lipid domain morphology during hemifusion |
title_sort | real-time intermembrane force measurements and imaging of lipid domain morphology during hemifusion |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4455132/ https://www.ncbi.nlm.nih.gov/pubmed/26006266 http://dx.doi.org/10.1038/ncomms8238 |
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