The cross-correlation-based analysis to digest the conformational dynamics of the mitoBK channels in terms of their modulation by flavonoids

IF 2.2 4区 生物学 Q3 BIOPHYSICS
Agata Wawrzkiewicz-Jałowiecka, Paulina Trybek, Beata Dworakowska, Piotr Bednarczyk, Przemysław Borys
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引用次数: 0

Abstract

The activity of mitochondrial large-conductance voltage- and \(Ca^{2+}\)-activated \(K^+\) channels (mitoBK) is regulated by a number of biochemical factors, including flavonoids. In particular, naringenin (Nar) and quercetin (Que) reached reasonable scientific attention due to their well-pronounced channel-activating effects. The open-reinforcing outcomes of Nar and Que on the mitoBK channel gating have been already reported. Nevertheless, the molecular picture of the corresponding channel–ligand interactions remains still to be revealed. In this work, we investigate the effects of the Nar and Que on the conformational dynamics of the mitoBK channel. In this aim, the cross-correlation-based analysis of the single-channel signals recorded by the patch-clamp method is performed. The obtained results in the form of phase space diagrams enable us to visually monitor the effects exerted by the considered flavonoids at the level of temporal characteristics of repetitive sequences of channel conformations. It turns out that the mitoBK channel activation by naringenin and quercetin does not lead to the change in the number of clusters within the phase space diagrams, which can be related to the constant number of available channel macroconformations regardless of the flavonoid administration. The localization and occupancy of the clusters of cross-correlated sequences suggest that mitoBK channel stimulation by flavonoids affects the relative stability of channel conformations and the kinetics of switching between them. For most clusters, greater net effects are observed in terms of quercetin administration in comparison with naringenin. It indicates stronger channel interaction with Que than Nar.

Abstract Image

基于互相关的分析,以消化mitoBK通道在黄酮类化合物调节方面的构象动力学。
线粒体大电导电压和[公式:见正文]激活的[公式:参见正文]通道(mitoBK)的活性受多种生物化学因子的调节,包括黄酮类化合物。特别是柚皮素(Nar)和槲皮素(Que)由于其显著的通道激活作用而引起了合理的科学关注。Nar和Que对mitoBK通道门控的开放增强结果已经报道。然而,相应的通道-配体相互作用的分子图谱仍有待揭示。在这项工作中,我们研究了Nar和Que对mitoBK通道构象动力学的影响。为此,对通过膜片钳方法记录的单通道信号进行基于互相关的分析。所获得的相空间图形式的结果使我们能够在通道构象重复序列的时间特征水平上直观地监测所考虑的黄酮类化合物所产生的影响。事实证明,柚皮素和槲皮素对mitoBK通道的激活不会导致相空间图中簇数的变化,这可能与可用通道大构象的恒定数量有关,而与类黄酮给药无关。交叉相关序列簇的定位和占据表明,黄酮类化合物对mitoBK通道的刺激影响通道构象的相对稳定性和它们之间转换的动力学。对于大多数聚类,与柚皮素相比,槲皮素给药的净效应更大。这表明与Que的通道交互比Nar更强。
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来源期刊
European Biophysics Journal
European Biophysics Journal 生物-生物物理
CiteScore
4.30
自引率
0.00%
发文量
43
审稿时长
6-12 weeks
期刊介绍: The journal publishes papers in the field of biophysics, which is defined as the study of biological phenomena by using physical methods and concepts. Original papers, reviews and Biophysics letters are published. The primary goal of this journal is to advance the understanding of biological structure and function by application of the principles of physical science, and by presenting the work in a biophysical context. Papers employing a distinctively biophysical approach at all levels of biological organisation will be considered, as will both experimental and theoretical studies. The criteria for acceptance are scientific content, originality and relevance to biological systems of current interest and importance. Principal areas of interest include: - Structure and dynamics of biological macromolecules - Membrane biophysics and ion channels - Cell biophysics and organisation - Macromolecular assemblies - Biophysical methods and instrumentation - Advanced microscopics - System dynamics.
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