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Nanoscopic substructures of raft-mimetic liquid-ordered membrane domains revealed by high-speed single-particle tracking
Lipid rafts are membrane nanodomains that facilitate important cell functions. Despite recent advances in identifying the biological significance of rafts, nature and regulation mechanism of rafts are largely unknown due to the difficulty of resolving dynamic molecular interaction of rafts at the na...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4997016/ https://www.ncbi.nlm.nih.gov/pubmed/26861908 http://dx.doi.org/10.1038/srep20542 |
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author | Wu, Hsiao-Mei Lin, Ying-Hsiu Yen, Tzu-Chi Hsieh, Chia-Lung |
author_facet | Wu, Hsiao-Mei Lin, Ying-Hsiu Yen, Tzu-Chi Hsieh, Chia-Lung |
author_sort | Wu, Hsiao-Mei |
collection | PubMed |
description | Lipid rafts are membrane nanodomains that facilitate important cell functions. Despite recent advances in identifying the biological significance of rafts, nature and regulation mechanism of rafts are largely unknown due to the difficulty of resolving dynamic molecular interaction of rafts at the nanoscale. Here, we investigate organization and single-molecule dynamics of rafts by monitoring lateral diffusion of single molecules in raft-containing reconstituted membranes supported on mica substrates. Using high-speed interferometric scattering (iSCAT) optical microscopy and small gold nanoparticles as labels, motion of single lipids is recorded via single-particle tracking (SPT) with nanometer spatial precision and microsecond temporal resolution. Processes of single molecules partitioning into and escaping from the raft-mimetic liquid-ordered (L(o)) domains are directly visualized in a continuous manner with unprecedented clarity. Importantly, we observe subdiffusion of saturated lipids in the L(o) domain in microsecond timescale, indicating the nanoscopic heterogeneous molecular arrangement of the L(o) domain. Further analysis of the diffusion trajectory shows the presence of nano-subdomains of the L(o) phase, as small as 10 nm, which transiently trap the lipids. Our results provide the first experimental evidence of non-uniform molecular organization of the L(o) phase, giving a new view of how rafts recruit and confine molecules in cell membranes. |
format | Online Article Text |
id | pubmed-4997016 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49970162016-08-30 Nanoscopic substructures of raft-mimetic liquid-ordered membrane domains revealed by high-speed single-particle tracking Wu, Hsiao-Mei Lin, Ying-Hsiu Yen, Tzu-Chi Hsieh, Chia-Lung Sci Rep Article Lipid rafts are membrane nanodomains that facilitate important cell functions. Despite recent advances in identifying the biological significance of rafts, nature and regulation mechanism of rafts are largely unknown due to the difficulty of resolving dynamic molecular interaction of rafts at the nanoscale. Here, we investigate organization and single-molecule dynamics of rafts by monitoring lateral diffusion of single molecules in raft-containing reconstituted membranes supported on mica substrates. Using high-speed interferometric scattering (iSCAT) optical microscopy and small gold nanoparticles as labels, motion of single lipids is recorded via single-particle tracking (SPT) with nanometer spatial precision and microsecond temporal resolution. Processes of single molecules partitioning into and escaping from the raft-mimetic liquid-ordered (L(o)) domains are directly visualized in a continuous manner with unprecedented clarity. Importantly, we observe subdiffusion of saturated lipids in the L(o) domain in microsecond timescale, indicating the nanoscopic heterogeneous molecular arrangement of the L(o) domain. Further analysis of the diffusion trajectory shows the presence of nano-subdomains of the L(o) phase, as small as 10 nm, which transiently trap the lipids. Our results provide the first experimental evidence of non-uniform molecular organization of the L(o) phase, giving a new view of how rafts recruit and confine molecules in cell membranes. Nature Publishing Group 2016-02-10 /pmc/articles/PMC4997016/ /pubmed/26861908 http://dx.doi.org/10.1038/srep20542 Text en Copyright © 2016, Macmillan Publishers Limited 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 Wu, Hsiao-Mei Lin, Ying-Hsiu Yen, Tzu-Chi Hsieh, Chia-Lung Nanoscopic substructures of raft-mimetic liquid-ordered membrane domains revealed by high-speed single-particle tracking |
title | Nanoscopic substructures of raft-mimetic liquid-ordered membrane domains revealed by high-speed single-particle tracking |
title_full | Nanoscopic substructures of raft-mimetic liquid-ordered membrane domains revealed by high-speed single-particle tracking |
title_fullStr | Nanoscopic substructures of raft-mimetic liquid-ordered membrane domains revealed by high-speed single-particle tracking |
title_full_unstemmed | Nanoscopic substructures of raft-mimetic liquid-ordered membrane domains revealed by high-speed single-particle tracking |
title_short | Nanoscopic substructures of raft-mimetic liquid-ordered membrane domains revealed by high-speed single-particle tracking |
title_sort | nanoscopic substructures of raft-mimetic liquid-ordered membrane domains revealed by high-speed single-particle tracking |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4997016/ https://www.ncbi.nlm.nih.gov/pubmed/26861908 http://dx.doi.org/10.1038/srep20542 |
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