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The Ionic Selectivity of Lysenin Channels in Open and Sub-Conducting States
The electrochemical gradients established across cell membranes are paramount for the execution of biological functions. Besides ion channels, other transporters, such as exogenous pore-forming toxins, may present ionic selectivity upon reconstitution in natural and artificial lipid membranes and co...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8622276/ https://www.ncbi.nlm.nih.gov/pubmed/34832126 http://dx.doi.org/10.3390/membranes11110897 |
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author | Bogard, Andrew Finn, Pangaea W. McKinney, Fulton Flacau, Ilinca M. Smith, Aviana R. Whiting, Rosey Fologea, Daniel |
author_facet | Bogard, Andrew Finn, Pangaea W. McKinney, Fulton Flacau, Ilinca M. Smith, Aviana R. Whiting, Rosey Fologea, Daniel |
author_sort | Bogard, Andrew |
collection | PubMed |
description | The electrochemical gradients established across cell membranes are paramount for the execution of biological functions. Besides ion channels, other transporters, such as exogenous pore-forming toxins, may present ionic selectivity upon reconstitution in natural and artificial lipid membranes and contribute to the electrochemical gradients. In this context, we utilized electrophysiology approaches to assess the ionic selectivity of the pore-forming toxin lysenin reconstituted in planar bilayer lipid membranes. The membrane voltages were determined from the reversal potentials recorded upon channel exposure to asymmetrical ionic conditions, and the permeability ratios were calculated from the fit with the Goldman–Hodgkin–Katz equation. Our work shows that lysenin channels are ion-selective and the determined permeability coefficients are cation and anion-species dependent. We also exploited the unique property of lysenin channels to transition to a stable sub-conducting state upon exposure to calcium ions and assessed their subsequent change in ionic selectivity. The observed loss of selectivity was implemented in an electrical model describing the dependency of reversal potentials on calcium concentration. In conclusion, our work demonstrates that this pore-forming toxin presents ionic selectivity but this is adjusted by the particular conduction state of the channels. |
format | Online Article Text |
id | pubmed-8622276 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-86222762021-11-27 The Ionic Selectivity of Lysenin Channels in Open and Sub-Conducting States Bogard, Andrew Finn, Pangaea W. McKinney, Fulton Flacau, Ilinca M. Smith, Aviana R. Whiting, Rosey Fologea, Daniel Membranes (Basel) Article The electrochemical gradients established across cell membranes are paramount for the execution of biological functions. Besides ion channels, other transporters, such as exogenous pore-forming toxins, may present ionic selectivity upon reconstitution in natural and artificial lipid membranes and contribute to the electrochemical gradients. In this context, we utilized electrophysiology approaches to assess the ionic selectivity of the pore-forming toxin lysenin reconstituted in planar bilayer lipid membranes. The membrane voltages were determined from the reversal potentials recorded upon channel exposure to asymmetrical ionic conditions, and the permeability ratios were calculated from the fit with the Goldman–Hodgkin–Katz equation. Our work shows that lysenin channels are ion-selective and the determined permeability coefficients are cation and anion-species dependent. We also exploited the unique property of lysenin channels to transition to a stable sub-conducting state upon exposure to calcium ions and assessed their subsequent change in ionic selectivity. The observed loss of selectivity was implemented in an electrical model describing the dependency of reversal potentials on calcium concentration. In conclusion, our work demonstrates that this pore-forming toxin presents ionic selectivity but this is adjusted by the particular conduction state of the channels. MDPI 2021-11-19 /pmc/articles/PMC8622276/ /pubmed/34832126 http://dx.doi.org/10.3390/membranes11110897 Text en © 2021 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 Bogard, Andrew Finn, Pangaea W. McKinney, Fulton Flacau, Ilinca M. Smith, Aviana R. Whiting, Rosey Fologea, Daniel The Ionic Selectivity of Lysenin Channels in Open and Sub-Conducting States |
title | The Ionic Selectivity of Lysenin Channels in Open and Sub-Conducting States |
title_full | The Ionic Selectivity of Lysenin Channels in Open and Sub-Conducting States |
title_fullStr | The Ionic Selectivity of Lysenin Channels in Open and Sub-Conducting States |
title_full_unstemmed | The Ionic Selectivity of Lysenin Channels in Open and Sub-Conducting States |
title_short | The Ionic Selectivity of Lysenin Channels in Open and Sub-Conducting States |
title_sort | ionic selectivity of lysenin channels in open and sub-conducting states |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8622276/ https://www.ncbi.nlm.nih.gov/pubmed/34832126 http://dx.doi.org/10.3390/membranes11110897 |
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