Cargando…
Impact of Glycans on Lipid Membrane Dynamics at the Nanoscale Unveiled by Planar Plasmonic Nanogap Antennas and Atomic Force Spectroscopy
[Image: see text] Lateral compartmentalization of the plasma membrane is a prominent feature present at multiple spatiotemporal scales that regulates key cellular functions. The extracellular glycocalyx matrix has recently emerged as an important player that modulates the organization of specific re...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7869103/ https://www.ncbi.nlm.nih.gov/pubmed/33480693 http://dx.doi.org/10.1021/acs.jpclett.0c03439 |
_version_ | 1783648564275052544 |
---|---|
author | Winkler, Pamina M. Campelo, Felix Giannotti, Marina I. Garcia-Parajo, Maria F. |
author_facet | Winkler, Pamina M. Campelo, Felix Giannotti, Marina I. Garcia-Parajo, Maria F. |
author_sort | Winkler, Pamina M. |
collection | PubMed |
description | [Image: see text] Lateral compartmentalization of the plasma membrane is a prominent feature present at multiple spatiotemporal scales that regulates key cellular functions. The extracellular glycocalyx matrix has recently emerged as an important player that modulates the organization of specific receptors and patterns the lipid bilayer itself. However, experimental limitations in investigating its impact on the membrane nanoscale dynamics have hampered detailed studies. Here, we used photonic nanoantenna arrays combined with fluorescence correlation spectroscopy to investigate the influence of hyaluronic acid (HA), a prominent glycosaminoglycan, on the nanoscale organization of mimetic lipid bilayers. Using atomic force microscopy and force spectroscopy, we further correlated our dynamic measurements with the morphology and mechanical properties of bilayers at the nanoscale. Overall, we find that HA has a profound effect on the dynamics, nanoscale organization, and mechanical properties of lipid bilayers that are enriched in sphingolipids and/or cholesterol, such as those present in living cells. |
format | Online Article Text |
id | pubmed-7869103 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-78691032021-02-09 Impact of Glycans on Lipid Membrane Dynamics at the Nanoscale Unveiled by Planar Plasmonic Nanogap Antennas and Atomic Force Spectroscopy Winkler, Pamina M. Campelo, Felix Giannotti, Marina I. Garcia-Parajo, Maria F. J Phys Chem Lett [Image: see text] Lateral compartmentalization of the plasma membrane is a prominent feature present at multiple spatiotemporal scales that regulates key cellular functions. The extracellular glycocalyx matrix has recently emerged as an important player that modulates the organization of specific receptors and patterns the lipid bilayer itself. However, experimental limitations in investigating its impact on the membrane nanoscale dynamics have hampered detailed studies. Here, we used photonic nanoantenna arrays combined with fluorescence correlation spectroscopy to investigate the influence of hyaluronic acid (HA), a prominent glycosaminoglycan, on the nanoscale organization of mimetic lipid bilayers. Using atomic force microscopy and force spectroscopy, we further correlated our dynamic measurements with the morphology and mechanical properties of bilayers at the nanoscale. Overall, we find that HA has a profound effect on the dynamics, nanoscale organization, and mechanical properties of lipid bilayers that are enriched in sphingolipids and/or cholesterol, such as those present in living cells. American Chemical Society 2021-01-22 2021-02-04 /pmc/articles/PMC7869103/ /pubmed/33480693 http://dx.doi.org/10.1021/acs.jpclett.0c03439 Text en © 2021 The Authors. Published by American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes. |
spellingShingle | Winkler, Pamina M. Campelo, Felix Giannotti, Marina I. Garcia-Parajo, Maria F. Impact of Glycans on Lipid Membrane Dynamics at the Nanoscale Unveiled by Planar Plasmonic Nanogap Antennas and Atomic Force Spectroscopy |
title | Impact of Glycans on Lipid Membrane Dynamics at the
Nanoscale Unveiled by Planar Plasmonic Nanogap Antennas and Atomic
Force Spectroscopy |
title_full | Impact of Glycans on Lipid Membrane Dynamics at the
Nanoscale Unveiled by Planar Plasmonic Nanogap Antennas and Atomic
Force Spectroscopy |
title_fullStr | Impact of Glycans on Lipid Membrane Dynamics at the
Nanoscale Unveiled by Planar Plasmonic Nanogap Antennas and Atomic
Force Spectroscopy |
title_full_unstemmed | Impact of Glycans on Lipid Membrane Dynamics at the
Nanoscale Unveiled by Planar Plasmonic Nanogap Antennas and Atomic
Force Spectroscopy |
title_short | Impact of Glycans on Lipid Membrane Dynamics at the
Nanoscale Unveiled by Planar Plasmonic Nanogap Antennas and Atomic
Force Spectroscopy |
title_sort | impact of glycans on lipid membrane dynamics at the
nanoscale unveiled by planar plasmonic nanogap antennas and atomic
force spectroscopy |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7869103/ https://www.ncbi.nlm.nih.gov/pubmed/33480693 http://dx.doi.org/10.1021/acs.jpclett.0c03439 |
work_keys_str_mv | AT winklerpaminam impactofglycansonlipidmembranedynamicsatthenanoscaleunveiledbyplanarplasmonicnanogapantennasandatomicforcespectroscopy AT campelofelix impactofglycansonlipidmembranedynamicsatthenanoscaleunveiledbyplanarplasmonicnanogapantennasandatomicforcespectroscopy AT giannottimarinai impactofglycansonlipidmembranedynamicsatthenanoscaleunveiledbyplanarplasmonicnanogapantennasandatomicforcespectroscopy AT garciaparajomariaf impactofglycansonlipidmembranedynamicsatthenanoscaleunveiledbyplanarplasmonicnanogapantennasandatomicforcespectroscopy |