Inserm U1003, Equipe Labellisée par la Ligue Nationale Contre le Cancer, Université de Sciences et Technologies de Lille (USTL), F-59655, Villeneuve d'Ascq, France.
Laboratory of Excellence, Ion Channels Science and Therapeutics; Université Lille I Sciences et Technologies, Villeneuve d'Ascq, France.
Sci Rep. 2017 Oct 26;7(1):14082. doi: 10.1038/s41598-017-13968-y.
Intracellular ion channels are involved in multiple signaling processes, including such crucial ones as regulation of cellular motility and fate. With 95% of the cellular membrane belonging to intracellular organelles, it is hard to overestimate the importance of intracellular ion channels. Multiple studies have been performed on these channels over the years, however, a unified approach allowing not only to characterize their activity but also to study their regulation by partner proteins, analogous to the patch clamp "golden standard", is lacking. Here, we present a universal approach that combines the extraction of intracellular membrane fractions with the preparation of patchable substrates that allows to characterize these channels in endogenous protein environment and to study their regulation by partner proteins. We validate this method by characterizing activity of multiple intracellular ion channels localized to different organelles and by providing detailed electrophysiological characterization of the regulation of IPR activity by endogenous Bcl-2. Thus, after synthesis and reshaping of the well-established approaches, organelle membrane derived patch clamp provides the means to assess ion channels from arbitrary cellular membranes at the single channel level.
细胞内离子通道参与多种信号转导过程,包括调节细胞运动和命运等关键过程。由于 95%的细胞膜属于细胞内细胞器,因此细胞内离子通道的重要性怎么强调都不为过。多年来,人们对这些通道进行了多项研究,然而,目前缺乏一种既能对其活性进行特征描述,又能像膜片钳“金标准”一样研究其与伴侣蛋白相互作用的调控的统一方法。在这里,我们提出了一种通用的方法,将细胞内膜成分的提取与可贴片制备相结合,使我们能够在天然蛋白环境中对这些通道进行特征描述,并研究其与伴侣蛋白的相互作用的调控。我们通过对定位于不同细胞器的多种细胞内离子通道的活性进行特征描述,并对天然 Bcl-2 对 IPR 活性的调控进行详细的电生理特征描述,验证了这种方法的有效性。因此,在对已建立的方法进行综合和改进之后,细胞器膜衍生的膜片钳为在单通道水平上评估任意细胞膜上的离子通道提供了手段。