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C型和N型失活异源电压门控钾通道的数学模型。

Mathematical models of C-type and N-type inactivating heteromeric voltage gated potassium channels.

作者信息

McGahan Kees, Keener James

机构信息

Math Department, University of Utah, Salt Lake City, UT, United States.

出版信息

Front Cell Neurosci. 2024 Oct 8;18:1418125. doi: 10.3389/fncel.2024.1418125. eCollection 2024.

DOI:10.3389/fncel.2024.1418125
PMID:39440001
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11493646/
Abstract

Voltage gated potassium channels can be composed of either four identical, or different, pore-forming protein subunits. While the voltage gated channels with identical subunits have been extensively studied both physiologically and mathematically, those with multiple subunit types, termed heteromeric channels, have not been. Here we construct, and explore the predictive outputs of, mechanistic models for heteromeric voltage gated potassium channels that possess either N-type or C-type inactivation kinetics. For both types of inactivation, we first build Markov models of four identical pore-forming inactivating subunits. Combining this with previous results regarding non-inactivating heteromeric channels, we are able to define models for heteromeric channels containing both non-inactivating and inactivating subunits of any ratio. We simulate each model through three unique voltage clamp protocols to identify steady state properties. In doing so, we generate predictions about the impact of adding additional inactivating subunits on a total channel's kinetics. We show that while N-type inactivating subunits appear to have a non-linear impact on the level of inactivation the channel experiences, the effect of C-type inactivating subunits is almost linear. Finally, to combat the computational issues of working with a large number of state variables we define model reductions for both types of heteromeric channels. For the N-type heteromers we derive a quasi-steady-state approximation and indicate where the approximation is appropriate. With the C-type heteromers we are able to write an explicit model reduction bringing models of greater than 10 dimensions down to 2.

摘要

电压门控钾通道可由四个相同或不同的成孔蛋白亚基组成。虽然具有相同亚基的电压门控通道在生理学和数学方面都得到了广泛研究,但具有多种亚基类型的通道(称为异源通道)却未被如此研究。在此,我们构建并探索了具有N型或C型失活动力学的异源电压门控钾通道的机制模型的预测输出。对于这两种失活类型,我们首先构建了四个相同的成孔失活亚基的马尔可夫模型。将此与先前关于非失活异源通道的结果相结合,我们能够定义包含任何比例的非失活和失活亚基的异源通道模型。我们通过三种独特的电压钳制方案对每个模型进行模拟,以确定稳态特性。在此过程中,我们生成了关于添加额外失活亚基对总通道动力学影响的预测。我们表明,虽然N型失活亚基似乎对通道经历的失活水平有非线性影响,但C型失活亚基的影响几乎是线性的。最后,为了解决处理大量状态变量时的计算问题,我们为两种类型的异源通道定义了模型简化方法。对于N型异源体,我们推导了一个准稳态近似,并指出该近似适用的情况。对于C型异源体,我们能够写出一个显式的模型简化方法,将大于10维的模型降至2维。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bc4/11493646/6f6536690759/fncel-18-1418125-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bc4/11493646/608387190716/fncel-18-1418125-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bc4/11493646/da8b30c4ce71/fncel-18-1418125-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bc4/11493646/e89fb6045810/fncel-18-1418125-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bc4/11493646/637346159fcc/fncel-18-1418125-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bc4/11493646/321e8611ff0d/fncel-18-1418125-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bc4/11493646/6f6536690759/fncel-18-1418125-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bc4/11493646/608387190716/fncel-18-1418125-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bc4/11493646/da8b30c4ce71/fncel-18-1418125-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bc4/11493646/e89fb6045810/fncel-18-1418125-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bc4/11493646/637346159fcc/fncel-18-1418125-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bc4/11493646/321e8611ff0d/fncel-18-1418125-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bc4/11493646/6f6536690759/fncel-18-1418125-g0007.jpg

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2
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Front Cell Neurosci. 2022 Nov 10;16:1036813. doi: 10.3389/fncel.2022.1036813. eCollection 2022.
3
Structure of the Shaker Kv channel and mechanism of slow C-type inactivation.摇椅式钾离子通道的结构与慢速C型失活机制
Sci Adv. 2022 Mar 18;8(11):eabm7814. doi: 10.1126/sciadv.abm7814.
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