Cargando…

AFM nanoindentation reveals decrease of elastic modulus of lipid bilayers near freezing point of water

Cell lipid membranes are the primary site of irreversible injury during freezing/thawing and cryopreservation of cells, but the underlying causes remain unknown. Here, we probe the effect of cooling from 20 °C to 0 °C on the structure and mechanical properties of 1,2-dipalmitoyl-sn-glycero-3-phospho...

Descripción completa

Detalles Bibliográficos
Autores principales: Gabbutt, Calum, Shen, Wuyi, Seifert, Jacob, Contera, Sonia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6923397/
https://www.ncbi.nlm.nih.gov/pubmed/31857622
http://dx.doi.org/10.1038/s41598-019-55519-7
_version_ 1783481523807191040
author Gabbutt, Calum
Shen, Wuyi
Seifert, Jacob
Contera, Sonia
author_facet Gabbutt, Calum
Shen, Wuyi
Seifert, Jacob
Contera, Sonia
author_sort Gabbutt, Calum
collection PubMed
description Cell lipid membranes are the primary site of irreversible injury during freezing/thawing and cryopreservation of cells, but the underlying causes remain unknown. Here, we probe the effect of cooling from 20 °C to 0 °C on the structure and mechanical properties of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) bilayers using atomic force microscopy (AFM) imaging and AFM-based nanoindentation in a liquid environment. The Young’s modulus of elasticity (E) at each temperature for DPPC was obtained at different ionic strengths. Both at 20 mM and 150 mM NaCl, E of DPPC bilayers increases exponentially –as expected–as the temperature is lowered between 20 °C and 5 °C, but at 0 °C E drops from the values measured at 5 °C. Our results support the hypothesis that mechanical weakening of the bilayer at 0 °C  is produced by  structural changes at the lipid-fluid interface.
format Online
Article
Text
id pubmed-6923397
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-69233972019-12-20 AFM nanoindentation reveals decrease of elastic modulus of lipid bilayers near freezing point of water Gabbutt, Calum Shen, Wuyi Seifert, Jacob Contera, Sonia Sci Rep Article Cell lipid membranes are the primary site of irreversible injury during freezing/thawing and cryopreservation of cells, but the underlying causes remain unknown. Here, we probe the effect of cooling from 20 °C to 0 °C on the structure and mechanical properties of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) bilayers using atomic force microscopy (AFM) imaging and AFM-based nanoindentation in a liquid environment. The Young’s modulus of elasticity (E) at each temperature for DPPC was obtained at different ionic strengths. Both at 20 mM and 150 mM NaCl, E of DPPC bilayers increases exponentially –as expected–as the temperature is lowered between 20 °C and 5 °C, but at 0 °C E drops from the values measured at 5 °C. Our results support the hypothesis that mechanical weakening of the bilayer at 0 °C  is produced by  structural changes at the lipid-fluid interface. Nature Publishing Group UK 2019-12-19 /pmc/articles/PMC6923397/ /pubmed/31857622 http://dx.doi.org/10.1038/s41598-019-55519-7 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Gabbutt, Calum
Shen, Wuyi
Seifert, Jacob
Contera, Sonia
AFM nanoindentation reveals decrease of elastic modulus of lipid bilayers near freezing point of water
title AFM nanoindentation reveals decrease of elastic modulus of lipid bilayers near freezing point of water
title_full AFM nanoindentation reveals decrease of elastic modulus of lipid bilayers near freezing point of water
title_fullStr AFM nanoindentation reveals decrease of elastic modulus of lipid bilayers near freezing point of water
title_full_unstemmed AFM nanoindentation reveals decrease of elastic modulus of lipid bilayers near freezing point of water
title_short AFM nanoindentation reveals decrease of elastic modulus of lipid bilayers near freezing point of water
title_sort afm nanoindentation reveals decrease of elastic modulus of lipid bilayers near freezing point of water
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6923397/
https://www.ncbi.nlm.nih.gov/pubmed/31857622
http://dx.doi.org/10.1038/s41598-019-55519-7
work_keys_str_mv AT gabbuttcalum afmnanoindentationrevealsdecreaseofelasticmodulusoflipidbilayersnearfreezingpointofwater
AT shenwuyi afmnanoindentationrevealsdecreaseofelasticmodulusoflipidbilayersnearfreezingpointofwater
AT seifertjacob afmnanoindentationrevealsdecreaseofelasticmodulusoflipidbilayersnearfreezingpointofwater
AT conterasonia afmnanoindentationrevealsdecreaseofelasticmodulusoflipidbilayersnearfreezingpointofwater