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Ann Neurol. 2019 Dec;86(6):899-912. doi: 10.1002/ana.25607. Epub 2019 Oct 24.
2
The S6 gate in regulatory Kv6 subunits restricts heteromeric K channel stoichiometry.S6 门控在调节性 Kv6 亚基中限制异源 K 通道的计量比。
J Gen Physiol. 2018 Dec 3;150(12):1702-1721. doi: 10.1085/jgp.201812121. Epub 2018 Oct 15.
3
Optimal fluorescent protein tags for quantifying protein oligomerization in living cells.最佳荧光蛋白标签用于定量活细胞中蛋白质寡聚化。
Sci Rep. 2018 Jul 13;8(1):10634. doi: 10.1038/s41598-018-28858-0.
4
α-SNAP regulates dynamic, on-site assembly and calcium selectivity of Orai1 channels.α-SNAP调节Orai1通道的动态、原位组装和钙选择性。
Mol Biol Cell. 2016 Aug 15;27(16):2542-53. doi: 10.1091/mbc.E16-03-0163. Epub 2016 Jun 22.
5
Kv5, Kv6, Kv8, and Kv9 subunits: No simple silent bystanders.Kv5、Kv6、Kv8和Kv9亚基:并非简单的沉默旁观者。
J Gen Physiol. 2016 Feb;147(2):105-25. doi: 10.1085/jgp.201511507. Epub 2016 Jan 11.
6
Automated Analysis of Single-Molecule Photobleaching Data by Statistical Modeling of Spot Populations.通过斑点群体的统计建模对单分子光漂白数据进行自动化分析
Biophys J. 2015 Dec 1;109(11):2352-62. doi: 10.1016/j.bpj.2015.10.035.
7
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PLoS One. 2015 Oct 27;10(10):e0141349. doi: 10.1371/journal.pone.0141349. eCollection 2015.
8
Plasma membrane dynamics and tetrameric organisation of ABCG2 transporters in mammalian cells revealed by single particle imaging techniques.单颗粒成像技术揭示哺乳动物细胞中ABCG2转运蛋白的质膜动力学和四聚体组织
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9
One, two or three? Probing the stoichiometry of membrane proteins by single-molecule localization microscopy.一个、两个还是三个?通过单分子定位显微镜探究膜蛋白的化学计量学。
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10
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确定 Kv2.1/Kv6.4 异四聚体的正确化学计量比,该异四聚体在多种化学计量比构象下具有功能。

Determining the correct stoichiometry of Kv2.1/Kv6.4 heterotetramers, functional in multiple stoichiometrical configurations.

机构信息

Department of Biochemistry, Université de Montréal, Montréal, QC, Canada H3C 3J7.

Laboratory for Molecular, Cellular and Network Excitability, Department of Biomedical Sciences, University of Antwerp, 2000 Antwerp, Belgium.

出版信息

Proc Natl Acad Sci U S A. 2020 Apr 28;117(17):9365-9376. doi: 10.1073/pnas.1916166117. Epub 2020 Apr 13.

DOI:10.1073/pnas.1916166117
PMID:32284408
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7196910/
Abstract

The electrically silent (KvS) members of the voltage-gated potassium (Kv) subfamilies Kv5, Kv6, Kv8, and Kv9 selectively modulate Kv2 subunits by forming heterotetrameric Kv2/KvS channels. Based on the reported 3:1 stoichiometry of Kv2.1/Kv9.3 channels, we tested the hypothesis that Kv2.1/Kv6.4 channels express, in contrast to the assumed 3:1, in a 2:2 stoichiometry. We investigate the Kv2.1/Kv6.4 stoichiometry using single subunit counting and functional characterization of tetrameric concatemers. For selecting the most probable stoichiometry, we introduce a model-selection method that is applicable for any multimeric complex by investigating the stoichiometry of Kv2.1/Kv6.4 channels. Weighted likelihood calculations bring rigor to a powerful technique. Using the weighted-likelihood model-selection method and analysis of electrophysiological data, we show that Kv2.1/Kv6.4 channels express, in contrast to the assumed 3:1, in a 2:2 stoichiometry. Within this stoichiometry, the Kv6.4 subunits have to be positioned alternating with Kv2.1 to express functional channels. The variability in Kv2/KvS assembly increases the diversity of heterotetrameric configurations and extends the regulatory possibilities of KvS by allowing the presence of more than one silent subunit.

摘要

电压门控钾 (Kv) 亚家族 Kv5、Kv6、Kv8 和 Kv9 的电静默 (KvS) 成员通过形成异四聚体 Kv2/KvS 通道选择性调节 Kv2 亚基。基于已报道的 Kv2.1/Kv9.3 通道 3:1 的比例,我们假设 Kv2.1/Kv6.4 通道的表达比例不是 3:1,而是 2:2。我们使用单体计数和四聚体串的功能表征来研究 Kv2.1/Kv6.4 通道的比例。为了选择最可能的比例,我们通过研究 Kv2.1/Kv6.4 通道的比例,引入了一种适用于任何多聚体复合物的模型选择方法。加权似然计算为强大的技术带来了严谨性。使用加权似然模型选择方法和电生理数据分析,我们表明 Kv2.1/Kv6.4 通道的表达比例不是 3:1,而是 2:2。在这种比例下,Kv6.4 亚基必须与 Kv2.1 交替排列才能表达功能性通道。Kv2/KvS 组装的可变性增加了异四聚体构象的多样性,并通过允许存在一个以上的静默亚基,扩展了 KvS 的调节可能性。