Cargando…
Ion-Induced Transient Potential Fluctuations Facilitate Pore Formation and Cation Transport through Lipid Membranes
[Image: see text] Unassisted ion transport through lipid membranes plays a crucial role in many cell functions without which life would not be possible, yet the precise mechanism behind the process remains unknown due to its molecular complexity. Here, we demonstrate a direct link between membrane p...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9801421/ https://www.ncbi.nlm.nih.gov/pubmed/36521841 http://dx.doi.org/10.1021/jacs.2c08543 |
_version_ | 1784861494018572288 |
---|---|
author | Roesel, David Eremchev, Maksim Poojari, Chetan S. Hub, Jochen S. Roke, Sylvie |
author_facet | Roesel, David Eremchev, Maksim Poojari, Chetan S. Hub, Jochen S. Roke, Sylvie |
author_sort | Roesel, David |
collection | PubMed |
description | [Image: see text] Unassisted ion transport through lipid membranes plays a crucial role in many cell functions without which life would not be possible, yet the precise mechanism behind the process remains unknown due to its molecular complexity. Here, we demonstrate a direct link between membrane potential fluctuations and divalent ion transport. High-throughput wide-field non-resonant second harmonic (SH) microscopy of membrane water shows that membrane potential fluctuations are universally found in lipid bilayer systems. Molecular dynamics simulations reveal that such variations in membrane potential reduce the free energy cost of transient pore formation and increase the ion flux across an open pore. These transient pores can act as conduits for ion transport, which we SH image for a series of divalent cations (Cu(2+), Ca(2+), Ba(2+), Mg(2+)) passing through giant unilamellar vesicle (GUV) membranes. Combining the experimental and computational results, we show that permeation through pores formed via an ion-induced electrostatic field is a viable mechanism for unassisted ion transport. |
format | Online Article Text |
id | pubmed-9801421 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-98014212022-12-31 Ion-Induced Transient Potential Fluctuations Facilitate Pore Formation and Cation Transport through Lipid Membranes Roesel, David Eremchev, Maksim Poojari, Chetan S. Hub, Jochen S. Roke, Sylvie J Am Chem Soc [Image: see text] Unassisted ion transport through lipid membranes plays a crucial role in many cell functions without which life would not be possible, yet the precise mechanism behind the process remains unknown due to its molecular complexity. Here, we demonstrate a direct link between membrane potential fluctuations and divalent ion transport. High-throughput wide-field non-resonant second harmonic (SH) microscopy of membrane water shows that membrane potential fluctuations are universally found in lipid bilayer systems. Molecular dynamics simulations reveal that such variations in membrane potential reduce the free energy cost of transient pore formation and increase the ion flux across an open pore. These transient pores can act as conduits for ion transport, which we SH image for a series of divalent cations (Cu(2+), Ca(2+), Ba(2+), Mg(2+)) passing through giant unilamellar vesicle (GUV) membranes. Combining the experimental and computational results, we show that permeation through pores formed via an ion-induced electrostatic field is a viable mechanism for unassisted ion transport. American Chemical Society 2022-12-15 2022-12-28 /pmc/articles/PMC9801421/ /pubmed/36521841 http://dx.doi.org/10.1021/jacs.2c08543 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Roesel, David Eremchev, Maksim Poojari, Chetan S. Hub, Jochen S. Roke, Sylvie Ion-Induced Transient Potential Fluctuations Facilitate Pore Formation and Cation Transport through Lipid Membranes |
title | Ion-Induced Transient
Potential Fluctuations Facilitate
Pore Formation and Cation Transport through Lipid Membranes |
title_full | Ion-Induced Transient
Potential Fluctuations Facilitate
Pore Formation and Cation Transport through Lipid Membranes |
title_fullStr | Ion-Induced Transient
Potential Fluctuations Facilitate
Pore Formation and Cation Transport through Lipid Membranes |
title_full_unstemmed | Ion-Induced Transient
Potential Fluctuations Facilitate
Pore Formation and Cation Transport through Lipid Membranes |
title_short | Ion-Induced Transient
Potential Fluctuations Facilitate
Pore Formation and Cation Transport through Lipid Membranes |
title_sort | ion-induced transient
potential fluctuations facilitate
pore formation and cation transport through lipid membranes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9801421/ https://www.ncbi.nlm.nih.gov/pubmed/36521841 http://dx.doi.org/10.1021/jacs.2c08543 |
work_keys_str_mv | AT roeseldavid ioninducedtransientpotentialfluctuationsfacilitateporeformationandcationtransportthroughlipidmembranes AT eremchevmaksim ioninducedtransientpotentialfluctuationsfacilitateporeformationandcationtransportthroughlipidmembranes AT poojarichetans ioninducedtransientpotentialfluctuationsfacilitateporeformationandcationtransportthroughlipidmembranes AT hubjochens ioninducedtransientpotentialfluctuationsfacilitateporeformationandcationtransportthroughlipidmembranes AT rokesylvie ioninducedtransientpotentialfluctuationsfacilitateporeformationandcationtransportthroughlipidmembranes |