IDEAS home Printed from https://ideas.repec.org/a/plo/pcbi00/1013078.html

One model to rule them all: Unification of voltage-gated potassium channel models via deep non-linear mixed effects modelling

Author

Listed:
  • Domas Linkevicius
  • Angus Chadwick
  • Melanie I Stefan
  • David C Sterratt

Abstract

Ion channels are essential for signal processing and propagation in neural cells. Voltage-gated ion channels permeable to potassium (Kv) form one of the most prominent channel families. Techniques used to model the voltage-dependent gating of Kv channels date back to Hodgkin and Huxley (1952). Different Kv types can display radically different kinetic properties, requiring different mathematical models. However, the construction of Hodgkin-Huxley-like (HH-like) models is generally complex and time consuming due to the number of parameters, their tuning and having to choose functional forms to model gating. In addition to the between-Kv type heterogeneity, there can be significant within-Kv type kinetic heterogeneity between different cells with genetically identical channels. Since HH-like models do not account for such variability, extensions to it are necessary. We use scientific machine learning (SciML), the integration of machine learning methodologies with existing scientific models, and non-linear mixed effects (NLME) modelling to bypass the limitations of HH-like modelling. NLME is a modelling methodology that takes into account both within- and between-subject variability. These tools allowed us to complement the HH-like modelling and construct a unified SciML HH-like model that fits the recordings from 20 different Kv types. The unified SciML HH-like model produced closer fits to the data compared to a set of seven previous HH-like models and was able to represent the highly heterogeneous data from different cells. Our model may be the first step in producing a SciML foundation model for ion channels that would be capable of modelling the gating kinetics of any ion channel type.Author summary: Ion channels are complex molecules embedded in the membranes of neurons – the cells responsible for signal propagation and processing in the brain. Ion channels can open and close in response to various types of stimuli, in particular the voltage difference across the cell membrane. Computational modelling, usage of mathematical techniques to represent a system and algorithmically solve for its dynamics, has been previously used to understand the dynamics of voltage-gated ion channels. However, computational modelling of voltage-gated ion channels requires costly and complex optimization routines to fit their structure and parameters. We utilize two tools new to the modelling of voltage-gated ion channels – scientific machine learning and non-linear mixed effects modelling – to bypass some limitations associated with the existing methods.

Suggested Citation

  • Domas Linkevicius & Angus Chadwick & Melanie I Stefan & David C Sterratt, 2026. "One model to rule them all: Unification of voltage-gated potassium channel models via deep non-linear mixed effects modelling," PLOS Computational Biology, Public Library of Science, vol. 22(4), pages 1-33, April.
  • Handle: RePEc:plo:pcbi00:1013078
    DOI: 10.1371/journal.pcbi.1013078
    as

    Download full text from publisher

    File URL: https://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1013078
    Download Restriction: no

    File URL: https://journals.plos.org/ploscompbiol/article/file?id=10.1371/journal.pcbi.1013078&type=printable
    Download Restriction: no

    File URL: https://libkey.io/10.1371/journal.pcbi.1013078?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:plo:pcbi00:1013078. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: ploscompbiol (email available below). General contact details of provider: https://journals.plos.org/ploscompbiol/ .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.