Cargando…

Real Space and Time Imaging of Collective Headgroup Dipole Motions in Zwitterionic Lipid Bilayers

Lipid bilayers are supramolecular structures responsible for a range of processes, such as transmembrane transport of ions and solutes, and sorting and replication of genetic materials, to name just a few. Some of these processes are transient and currently, cannot be visualized in real space and ti...

Descripción completa

Detalles Bibliográficos
Autores principales: Bolmatov, Dima, Collier, C. Patrick, Zav’yalov, Dmitry, Egami, Takeshi, Katsaras, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10142431/
https://www.ncbi.nlm.nih.gov/pubmed/37103869
http://dx.doi.org/10.3390/membranes13040442
_version_ 1785033612322668544
author Bolmatov, Dima
Collier, C. Patrick
Zav’yalov, Dmitry
Egami, Takeshi
Katsaras, John
author_facet Bolmatov, Dima
Collier, C. Patrick
Zav’yalov, Dmitry
Egami, Takeshi
Katsaras, John
author_sort Bolmatov, Dima
collection PubMed
description Lipid bilayers are supramolecular structures responsible for a range of processes, such as transmembrane transport of ions and solutes, and sorting and replication of genetic materials, to name just a few. Some of these processes are transient and currently, cannot be visualized in real space and time. Here, we developed an approach using 1D, 2D, and 3D Van Hove correlation functions to image collective headgroup dipole motions in zwitterionic phospholipid bilayers. We show that both 2D and 3D spatiotemporal images of headgroup dipoles are consistent with commonly understood dynamic features of fluids. However, analysis of the 1D Van Hove function reveals lateral transient and re-emergent collective dynamics of the headgroup dipoles—occurring at picosecond time scales—that transmit and dissipate heat at longer times, due to relaxation processes. At the same time, the headgroup dipoles also generate membrane surface undulations due a collective tilting of the headgroup dipoles. A continuous intensity band of headgroup dipole spatiotemporal correlations—at nanometer length and nanosecond time scales—indicates that dipoles undergo stretching and squeezing elastic deformations. Importantly, the above mentioned intrinsic headgroup dipole motions can be externally stimulated at GHz-frequency scale, enhancing their flexoelectric and piezoelectric capabilities (i.e., increased conversion efficiency of mechanical energy into electric energy). In conclusion, we discuss how lipid membranes can provide molecular-level insights about biological learning and memory, and as platforms for the development of the next generation of neuromorphic computers.
format Online
Article
Text
id pubmed-10142431
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-101424312023-04-29 Real Space and Time Imaging of Collective Headgroup Dipole Motions in Zwitterionic Lipid Bilayers Bolmatov, Dima Collier, C. Patrick Zav’yalov, Dmitry Egami, Takeshi Katsaras, John Membranes (Basel) Article Lipid bilayers are supramolecular structures responsible for a range of processes, such as transmembrane transport of ions and solutes, and sorting and replication of genetic materials, to name just a few. Some of these processes are transient and currently, cannot be visualized in real space and time. Here, we developed an approach using 1D, 2D, and 3D Van Hove correlation functions to image collective headgroup dipole motions in zwitterionic phospholipid bilayers. We show that both 2D and 3D spatiotemporal images of headgroup dipoles are consistent with commonly understood dynamic features of fluids. However, analysis of the 1D Van Hove function reveals lateral transient and re-emergent collective dynamics of the headgroup dipoles—occurring at picosecond time scales—that transmit and dissipate heat at longer times, due to relaxation processes. At the same time, the headgroup dipoles also generate membrane surface undulations due a collective tilting of the headgroup dipoles. A continuous intensity band of headgroup dipole spatiotemporal correlations—at nanometer length and nanosecond time scales—indicates that dipoles undergo stretching and squeezing elastic deformations. Importantly, the above mentioned intrinsic headgroup dipole motions can be externally stimulated at GHz-frequency scale, enhancing their flexoelectric and piezoelectric capabilities (i.e., increased conversion efficiency of mechanical energy into electric energy). In conclusion, we discuss how lipid membranes can provide molecular-level insights about biological learning and memory, and as platforms for the development of the next generation of neuromorphic computers. MDPI 2023-04-18 /pmc/articles/PMC10142431/ /pubmed/37103869 http://dx.doi.org/10.3390/membranes13040442 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Bolmatov, Dima
Collier, C. Patrick
Zav’yalov, Dmitry
Egami, Takeshi
Katsaras, John
Real Space and Time Imaging of Collective Headgroup Dipole Motions in Zwitterionic Lipid Bilayers
title Real Space and Time Imaging of Collective Headgroup Dipole Motions in Zwitterionic Lipid Bilayers
title_full Real Space and Time Imaging of Collective Headgroup Dipole Motions in Zwitterionic Lipid Bilayers
title_fullStr Real Space and Time Imaging of Collective Headgroup Dipole Motions in Zwitterionic Lipid Bilayers
title_full_unstemmed Real Space and Time Imaging of Collective Headgroup Dipole Motions in Zwitterionic Lipid Bilayers
title_short Real Space and Time Imaging of Collective Headgroup Dipole Motions in Zwitterionic Lipid Bilayers
title_sort real space and time imaging of collective headgroup dipole motions in zwitterionic lipid bilayers
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10142431/
https://www.ncbi.nlm.nih.gov/pubmed/37103869
http://dx.doi.org/10.3390/membranes13040442
work_keys_str_mv AT bolmatovdima realspaceandtimeimagingofcollectiveheadgroupdipolemotionsinzwitterioniclipidbilayers
AT colliercpatrick realspaceandtimeimagingofcollectiveheadgroupdipolemotionsinzwitterioniclipidbilayers
AT zavyalovdmitry realspaceandtimeimagingofcollectiveheadgroupdipolemotionsinzwitterioniclipidbilayers
AT egamitakeshi realspaceandtimeimagingofcollectiveheadgroupdipolemotionsinzwitterioniclipidbilayers
AT katsarasjohn realspaceandtimeimagingofcollectiveheadgroupdipolemotionsinzwitterioniclipidbilayers