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...

Descripción completa

Detalles Bibliográficos
Autores principales: Winkler, Pamina M., Campelo, Felix, Giannotti, Marina I., Garcia-Parajo, Maria F.
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