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Stoichiometry Studies Reveal Functional Properties of KDC1 in Plant Shaker Potassium Channels

机译:化学计量学研究揭示了KDC1在植物摇床钾通道中的功能特性

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摘要

Functional heteromeric plant Shaker potassium channels can be formed by the assembly of subunits from different tissues, as well as from diverse plant species. KDC1 (K+ Daucus carota 1) produces inward-rectifying currents in Xenopus oocytes when coexpressed with KAT1 and other subunits appertaining to different plant Shaker subfamilies. Owing to the presence of KDC1, resulting heteromeric channels display slower activation kinetics, a shift of the activation threshold toward more negative membrane potentials and current potentiation upon the addition of external zinc. Despite available information on heteromerization of plant Shaker channels, very little is known to date on the properties of the various stoichiometric configurations formed by different subunits. To investigate the functional properties of heteromeric nKDC1/mKAT1 configurations, we realized a series of dimeric constructs combining KDC1 and KAT1 α-subunits. We found that homomeric channels, formed by monomeric or dimeric α-subunit constructs, show identical biophysical characteristics. Coinjections of diverse tandem constructs, instead, displayed significantly different currents proving that KDC1 has high affinity for KAT1 and participates in the formation of functional channels with at most two KDC1 subunits, whereas three KDC1 subunits prevented the formation of functional channels. This article brings a contribution to the understanding of the molecular mechanisms regulating plant Shaker channel functionality by association of modulatory subunits.
机译:功能性异源植物摇床钾通道可通过组装来自不同组织以及不同植物物种的亚基来形成。当KDC1(K + Daucus carota 1)与KAT1和其他属于不同植物摇床亚科的亚基共表达时,它们在非洲爪蟾卵母细胞中产生内向整流电流。由于KDC1的存在,所得的异聚体通道显示出较慢的活化动力学,活化阈值向更多的负膜电位移动,并且在添加外部锌后电流增强。尽管可获得关于植物摇床通道异构化的可用信息,但是迄今为止对于由不同亚基形成的各种化学计量构型的性质知之甚少。为了研究异聚nKDC1 / mKAT1构型的功能特性,我们实现了一系列结合KDC1和KAT1α-亚基的二聚体构建体。我们发现,由单体或二聚体α-亚基构建体形成的同质通道显示出相同的生物物理特征。相反,多种串联构建体的共注射显示出明显不同的电流,证明KDC1对KAT1具有高亲和力,并参与具有最多两个KDC1亚基的功能通道的形成,而三个KDC1亚基阻止了功能通道的形成。本文通过调节亚基的结合为理解调节植物摇床通道功能的分子机制做出了贡献。

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