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Single-molecule localization to study cytoskeletal structures, membrane complexes, and mechanosensors

机译:单分子定位研究细胞骨骼结构,膜配合物和机械传感器

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In the last decades, a promising breakthrough in fluorescence imaging was represented by the advent of super-resolution microscopy (SRM). Super-resolution techniques recently became a popular method to study sub-cellular structures, providing a successful approach to observe cytoskeletal and focal adhesion proteins. Among the SR techniques, single-molecule localization microscopy plays a significant role due to its ability to unveil structures and molecular organizations in biological systems. Furthermore, since they provide information at the molecular level, these techniques are increasingly being used to study the stoichiometry and interaction between several membrane channel proteins and their accessory subunits. The aim of this review is to describe the single-molecule localization-based techniques and their applications relevant to cytoskeletal structures and membrane complexes in order to provide as future prospective an overall picture of their correlation with the mechanosensor channel expression and activity.
机译:在过去的几十年中,通过超分辨率显微镜(SRM)的出现来表示荧光成像的有希望的突破。超分辨率技术最近成为研究亚细胞结构的流行方法,提供了观察细胞骨骼和局灶性粘附蛋白的成功方法。在SR技术中,单分子定位显微镜由于其在生物系统中的结构和分子组织的能力而起着重要作用。此外,由于它们提供了分子水平的信息,因此越来越多地用于研究几种膜通道蛋白及其附属亚基之间的化学计量和相互作用。本综述的目的是描述基于单分子本地化的技术及其与细胞骨架结构和膜复合物相关的应用,以便提供与未来的前瞻性与机械传感器通道表达和活动的相关性。

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