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Maintaining sidedness and fluidity in cell membrane coatings supported on nano-particulate and planar surfaces
Supported cell membrane coatings meet many requirements set to bioactive nanocarriers and materials, provided sidedness and fluidity of the natural membrane are maintained upon coating. However, the properties of a support-surface responsible for maintaining correct sidedness and fluidity are unknow...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
KeAi Publishing
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10622627/ https://www.ncbi.nlm.nih.gov/pubmed/37927898 http://dx.doi.org/10.1016/j.bioactmat.2023.10.010 |
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author | Liu, Sidi Li, Yuanfeng Shi, Linqi Liu, Jian Ren, Yijin Laman, Jon D. van der Mei, Henny C. Busscher, Henk J. |
author_facet | Liu, Sidi Li, Yuanfeng Shi, Linqi Liu, Jian Ren, Yijin Laman, Jon D. van der Mei, Henny C. Busscher, Henk J. |
author_sort | Liu, Sidi |
collection | PubMed |
description | Supported cell membrane coatings meet many requirements set to bioactive nanocarriers and materials, provided sidedness and fluidity of the natural membrane are maintained upon coating. However, the properties of a support-surface responsible for maintaining correct sidedness and fluidity are unknown. Here, we briefly review the properties of natural membranes and membrane-isolation methods, with focus on the asymmetric distribution of functional groups in natural membranes (sidedness) and the ability of molecules to float across a membrane to form functional domains (fluidity). This review concludes that hydrophilic sugar-residues of glycoproteins in the outer-leaflet of cell membranes direct the more hydrophobic inner-leaflet towards a support-surface to create a correctly-sided membrane coating, regardless of electrostatic double-layer interactions. On positively-charged support-surfaces however, strong, electrostatic double-layer attraction of negatively-charged membranes can impede homogeneous coating. In correctly-sided membrane coatings, fluidity is maintained regardless of whether the surface carries a positive or negative charge. However, membranes are frozen on positively-charged, highly-curved, small nanoparticles and localized nanoscopic structures on a support-surface. This leaves an unsupported membrane coating in between nanostructures on planar support-surfaces that is in dual-sided contact with its aqueous environment, yielding enhanced fluidity in membrane coatings on nanostructured, planar support-surfaces as compared with smooth ones. |
format | Online Article Text |
id | pubmed-10622627 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | KeAi Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-106226272023-11-04 Maintaining sidedness and fluidity in cell membrane coatings supported on nano-particulate and planar surfaces Liu, Sidi Li, Yuanfeng Shi, Linqi Liu, Jian Ren, Yijin Laman, Jon D. van der Mei, Henny C. Busscher, Henk J. Bioact Mater Review Article Supported cell membrane coatings meet many requirements set to bioactive nanocarriers and materials, provided sidedness and fluidity of the natural membrane are maintained upon coating. However, the properties of a support-surface responsible for maintaining correct sidedness and fluidity are unknown. Here, we briefly review the properties of natural membranes and membrane-isolation methods, with focus on the asymmetric distribution of functional groups in natural membranes (sidedness) and the ability of molecules to float across a membrane to form functional domains (fluidity). This review concludes that hydrophilic sugar-residues of glycoproteins in the outer-leaflet of cell membranes direct the more hydrophobic inner-leaflet towards a support-surface to create a correctly-sided membrane coating, regardless of electrostatic double-layer interactions. On positively-charged support-surfaces however, strong, electrostatic double-layer attraction of negatively-charged membranes can impede homogeneous coating. In correctly-sided membrane coatings, fluidity is maintained regardless of whether the surface carries a positive or negative charge. However, membranes are frozen on positively-charged, highly-curved, small nanoparticles and localized nanoscopic structures on a support-surface. This leaves an unsupported membrane coating in between nanostructures on planar support-surfaces that is in dual-sided contact with its aqueous environment, yielding enhanced fluidity in membrane coatings on nanostructured, planar support-surfaces as compared with smooth ones. KeAi Publishing 2023-10-21 /pmc/articles/PMC10622627/ /pubmed/37927898 http://dx.doi.org/10.1016/j.bioactmat.2023.10.010 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Review Article Liu, Sidi Li, Yuanfeng Shi, Linqi Liu, Jian Ren, Yijin Laman, Jon D. van der Mei, Henny C. Busscher, Henk J. Maintaining sidedness and fluidity in cell membrane coatings supported on nano-particulate and planar surfaces |
title | Maintaining sidedness and fluidity in cell membrane coatings supported on nano-particulate and planar surfaces |
title_full | Maintaining sidedness and fluidity in cell membrane coatings supported on nano-particulate and planar surfaces |
title_fullStr | Maintaining sidedness and fluidity in cell membrane coatings supported on nano-particulate and planar surfaces |
title_full_unstemmed | Maintaining sidedness and fluidity in cell membrane coatings supported on nano-particulate and planar surfaces |
title_short | Maintaining sidedness and fluidity in cell membrane coatings supported on nano-particulate and planar surfaces |
title_sort | maintaining sidedness and fluidity in cell membrane coatings supported on nano-particulate and planar surfaces |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10622627/ https://www.ncbi.nlm.nih.gov/pubmed/37927898 http://dx.doi.org/10.1016/j.bioactmat.2023.10.010 |
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