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是时候引入熵时钟了:随机链蛋白序列在决定动作电位特性的离子通道过程计时中的作用。

It's Time for Entropic Clocks: The Roles of Random Chain Protein Sequences in Timing Ion Channel Processes Underlying Action Potential Properties.

作者信息

Nsasra Esraa, Dahan Irit, Eichler Jerry, Yifrach Ofer

机构信息

Department of Life Sciences, School of Brain Sciences and Cognition, Ben-Gurion University of the Negev, P.O. Box 653, Beer Sheva 84105, Israel.

出版信息

Entropy (Basel). 2023 Sep 17;25(9):1351. doi: 10.3390/e25091351.

DOI:10.3390/e25091351
PMID:37761650
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10527868/
Abstract

In recent years, it has become clear that intrinsically disordered protein segments play diverse functional roles in many cellular processes, thus leading to a reassessment of the classical structure-function paradigm. One class of intrinsically disordered protein segments is entropic clocks, corresponding to unstructured random protein chains involved in timing cellular processes. Such clocks were shown to modulate ion channel processes underlying action potential generation, propagation, and transmission. In this review, we survey the role of entropic clocks in timing intra- and inter-molecular binding events of voltage-activated potassium channels involved in gating and clustering processes, respectively, and where both are known to occur according to a similar 'ball and chain' mechanism. We begin by delineating the thermodynamic and timing signatures of a 'ball and chain'-based binding mechanism involving entropic clocks, followed by a detailed analysis of the use of such a mechanism in the prototypical voltage-activated K channel model protein, with particular emphasis on ion channel clustering. We demonstrate how 'chain'-level alternative splicing of the Kv channel gene modulates entropic clock-based 'ball and chain' inactivation and clustering channel functions. As such, the Kv channel model system exemplifies how linkage between alternative splicing and intrinsic disorder enables the functional diversity underlying changes in electrical signaling.

摘要

近年来,很明显内在无序蛋白片段在许多细胞过程中发挥着多样的功能作用,从而导致对经典结构-功能范式的重新评估。一类内在无序蛋白片段是熵钟,对应于参与细胞过程计时的无结构随机蛋白链。已表明此类时钟可调节动作电位产生、传播和传递所涉及的离子通道过程。在本综述中,我们分别探讨了熵钟在电压激活钾通道的分子内和分子间结合事件计时中的作用,这些结合事件分别涉及门控和聚集过程,并且已知两者均根据类似的“球与链”机制发生。我们首先描述基于熵钟的“球与链”结合机制的热力学和计时特征,随后详细分析这种机制在典型电压激活钾通道模型蛋白中的应用,特别强调离子通道聚集。我们展示了Kv通道基因的“链”水平可变剪接如何调节基于熵钟的“球与链”失活和聚集通道功能。因此,Kv通道模型系统例证了可变剪接与内在无序之间的联系如何实现电信号变化背后的功能多样性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78ef/10527868/91c135484646/entropy-25-01351-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78ef/10527868/a1263097cda3/entropy-25-01351-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78ef/10527868/8294ab814eb1/entropy-25-01351-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78ef/10527868/c11eb05be487/entropy-25-01351-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78ef/10527868/09eb118b4376/entropy-25-01351-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78ef/10527868/e052299a3dbf/entropy-25-01351-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78ef/10527868/91c135484646/entropy-25-01351-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78ef/10527868/a1263097cda3/entropy-25-01351-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78ef/10527868/8294ab814eb1/entropy-25-01351-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78ef/10527868/c11eb05be487/entropy-25-01351-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78ef/10527868/09eb118b4376/entropy-25-01351-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78ef/10527868/e052299a3dbf/entropy-25-01351-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78ef/10527868/91c135484646/entropy-25-01351-g006.jpg

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本文引用的文献

1
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2
Molecular and cellular correlates in Kv channel clustering: entropy-based regulation of cluster ion channel density.Kv 通道簇集的分子和细胞相关性:基于熵的簇离子通道密度调控。
Sci Rep. 2020 Jul 9;10(1):11304. doi: 10.1038/s41598-020-68003-4.
3
Clusters of cooperative ion channels enable a membrane-potential-based mechanism for short-term memory.
簇状协同离子通道为基于膜电位的短期记忆机制提供了可能。
Elife. 2020 Feb 7;9:e49974. doi: 10.7554/eLife.49974.
4
Direct Evidence for a Similar Molecular Mechanism Underlying Shaker Kv Channel Fast Inactivation and Clustering.直接证据表明 Shaker Kv 通道快速失活和聚集的分子机制相似。
J Mol Biol. 2019 Feb 1;431(3):542-556. doi: 10.1016/j.jmb.2018.12.002. Epub 2018 Dec 11.
5
Entropic clocks in the service of electrical signaling: 'Ball and chain' mechanisms for ion channel inactivation and clustering.服务于电信号传导的熵钟:离子通道失活与聚集的“球与链”机制
FEBS Lett. 2015 Sep 14;589(19 Pt A):2441-7. doi: 10.1016/j.febslet.2015.06.010. Epub 2015 Jun 22.
6
Alternative splicing modulates Kv channel clustering through a molecular ball and chain mechanism.可变剪接通过分子球链机制调节 Kv 通道簇集。
Nat Commun. 2015 Mar 27;6:6488. doi: 10.1038/ncomms7488.
7
Subcellular localization of K+ channels in mammalian brain neurons: remarkable precision in the midst of extraordinary complexity.哺乳动物脑神经元中钾通道的亚细胞定位:在极其复杂的环境中达到惊人的精确性。
Neuron. 2015 Jan 21;85(2):238-56. doi: 10.1016/j.neuron.2014.12.042.
8
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