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Modeling the kinetics of heteromeric potassium channels
Mechanistic mathematical modeling has long been used as a tool for answering questions in cellular physiology. To mathematically describe cellular processes such as cell excitability, volume regulation, neurotransmitter release, and hormone secretion requires accurate descriptions of ion channel kin...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9686856/ https://www.ncbi.nlm.nih.gov/pubmed/36439203 http://dx.doi.org/10.3389/fncel.2022.1036813 |
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author | McGahan, Kees Keener, James |
author_facet | McGahan, Kees Keener, James |
author_sort | McGahan, Kees |
collection | PubMed |
description | Mechanistic mathematical modeling has long been used as a tool for answering questions in cellular physiology. To mathematically describe cellular processes such as cell excitability, volume regulation, neurotransmitter release, and hormone secretion requires accurate descriptions of ion channel kinetics. One class of ion channels currently lacking a physiological model framework is the class of channels built with multiple different potassium protein subunits called heteromeric voltage gated potassium channels. Here we present a novel mathematical model for heteromeric potassium channels that captures both the number and type of protein subunits present in each channel. Key model assumptions are validated by showing our model is the reduction of a Markov model and through observations about voltage clamp data. We then show our model's success in replicating kinetic properties of concatemeric channels with different numbers of K(v)1.1 and K(v)1.2 subunits. Finally, through comparisons with multiple expression experiments across multiple voltage gated potassium families, we use the model to make predictions about the importance and effect of genetic mutations in heteromeric channel formation. |
format | Online Article Text |
id | pubmed-9686856 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96868562022-11-25 Modeling the kinetics of heteromeric potassium channels McGahan, Kees Keener, James Front Cell Neurosci Cellular Neuroscience Mechanistic mathematical modeling has long been used as a tool for answering questions in cellular physiology. To mathematically describe cellular processes such as cell excitability, volume regulation, neurotransmitter release, and hormone secretion requires accurate descriptions of ion channel kinetics. One class of ion channels currently lacking a physiological model framework is the class of channels built with multiple different potassium protein subunits called heteromeric voltage gated potassium channels. Here we present a novel mathematical model for heteromeric potassium channels that captures both the number and type of protein subunits present in each channel. Key model assumptions are validated by showing our model is the reduction of a Markov model and through observations about voltage clamp data. We then show our model's success in replicating kinetic properties of concatemeric channels with different numbers of K(v)1.1 and K(v)1.2 subunits. Finally, through comparisons with multiple expression experiments across multiple voltage gated potassium families, we use the model to make predictions about the importance and effect of genetic mutations in heteromeric channel formation. Frontiers Media S.A. 2022-11-10 /pmc/articles/PMC9686856/ /pubmed/36439203 http://dx.doi.org/10.3389/fncel.2022.1036813 Text en Copyright © 2022 McGahan and Keener. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cellular Neuroscience McGahan, Kees Keener, James Modeling the kinetics of heteromeric potassium channels |
title | Modeling the kinetics of heteromeric potassium channels |
title_full | Modeling the kinetics of heteromeric potassium channels |
title_fullStr | Modeling the kinetics of heteromeric potassium channels |
title_full_unstemmed | Modeling the kinetics of heteromeric potassium channels |
title_short | Modeling the kinetics of heteromeric potassium channels |
title_sort | modeling the kinetics of heteromeric potassium channels |
topic | Cellular Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9686856/ https://www.ncbi.nlm.nih.gov/pubmed/36439203 http://dx.doi.org/10.3389/fncel.2022.1036813 |
work_keys_str_mv | AT mcgahankees modelingthekineticsofheteromericpotassiumchannels AT keenerjames modelingthekineticsofheteromericpotassiumchannels |