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基于流形边界的离子通道模型约简。

Ion channel model reduction using manifold boundaries.

机构信息

Centre for Mathematical Medicine and Biology, School of Mathematical Sciences, University of Nottingham, Nottingham, UK.

Department of Biomedical Physiology and Kinesiology, Simon Fraser University, Burnaby, Canada.

出版信息

J R Soc Interface. 2022 Aug;19(193):20220193. doi: 10.1098/rsif.2022.0193. Epub 2022 Aug 10.

Abstract

Mathematical models of voltage-gated ion channels are used in basic research, industrial and clinical settings. These models range in complexity, but typically contain numerous variables representing the proportion of channels in a given state, and parameters describing the voltage-dependent rates of transition between states. An open problem is selecting the appropriate degree of complexity and structure for an ion channel model given data availability. Here, we simplify a model of the cardiac human Ether-à-go-go related gene (hERG) potassium ion channel, which carries cardiac , using the manifold boundary approximation method (MBAM). The MBAM approximates high-dimensional model-output manifolds by reduced models describing their boundaries, resulting in models with fewer parameters (and often variables). We produced a series of models of reducing complexity starting from an established five-state hERG model with 15 parameters. Models with up to three fewer states and eight fewer parameters were shown to retain much of the predictive capability of the full model and were validated using experimental hERG1a data collected in HEK293 cells at 37°C. The method provides a way to simplify complex models of ion channels that improves parameter identifiability and will aid in future model development.

摘要

电压门控离子通道的数学模型被用于基础研究、工业和临床环境。这些模型的复杂程度不一,但通常包含许多变量,代表给定状态下的通道比例,以及描述状态之间电压依赖性转换速率的参数。一个悬而未决的问题是,给定可用数据,如何为离子通道模型选择适当的复杂度和结构。在这里,我们使用流形边界逼近方法(MBAM)简化了一种心脏人类 Ether-à-go-go 相关基因(hERG)钾离子通道模型,该模型携带心脏。MBAM 通过描述其边界的简化模型来逼近高维模型输出流形,从而得到具有较少参数(通常变量也较少)的模型。我们从一个具有 15 个参数的既定五态 hERG 模型开始,生成了一系列简化复杂度的模型。结果表明,具有三个或更少状态和八个或更少参数的模型保留了全模型的大部分预测能力,并使用在 37°C 的 HEK293 细胞中收集的实验 hERG1a 数据进行了验证。该方法提供了一种简化离子通道复杂模型的方法,可提高参数可识别性,并有助于未来的模型开发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24d2/9363999/be79964d3741/rsif20220193f01.jpg

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