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活细胞中受体酪氨酸激酶寡聚化的光学测量。

Optical measurement of receptor tyrosine kinase oligomerization on live cells.

机构信息

Janelia Research Campus, Howard Hughes Medical Institute, 19700 Helix Drive, Ashburn, VA 20147, USA.

出版信息

Biochim Biophys Acta Biomembr. 2017 Sep;1859(9 Pt A):1436-1444. doi: 10.1016/j.bbamem.2017.03.026. Epub 2017 Apr 4.

Abstract

Receptor tyrosine kinases (RTK) are important cell surface receptors that transduce extracellular signals across the plasma membrane. The traditional view of how these receptors function is that ligand binding to the extracellular domains acts as a master-switch that enables receptor monomers to dimerize and subsequently trans-phosphorylate each other on their intracellular domains. However, a growing body of evidence suggests that receptor oligomerization is not merely a consequence of ligand binding, but is instead part of a complex process responsible for regulation of receptor activation. Importantly, the oligomerization dynamics and subsequent activation of these receptors are affected by other cellular components, such as cytoskeletal machineries and cell membrane lipid characteristics. Thus receptor activation is not an isolated molecular event mediated by the ligand-receptor interaction, but instead involves orchestrated interactions between the receptors and other cellular components. Measuring receptor oligomerization dynamics on live cells can yield important insights into the characteristics of these interactions. Therefore, it is imperative to develop techniques that can probe receptor movements on the plasma membrane with optimal temporal and spatial resolutions. Various microscopic techniques have been used for this purpose. Optical techniques including single molecule tracking (SMT) and fluorescence correlation spectroscopy (FCS) measure receptor diffusion on live cells. Receptor-receptor interactions can also be assessed by detecting Förster resonance energy transfer (FRET) between fluorescently-labeled receptors situated in close proximity or by counting the number of receptors within a diffraction limited fluorescence spot (stepwise bleaching). This review will describe recent developments of optical techniques that have been used to study receptor oligomerization on living cells. This article is part of a Special Issue entitled: Interactions between membrane receptors in cellular membranes edited by Kalina Hristova.

摘要

受体酪氨酸激酶 (RTK) 是一种重要的细胞表面受体,能够将细胞外信号转导穿过质膜。这些受体如何发挥作用的传统观点是,配体与细胞外结构域的结合充当主开关,使受体单体二聚化,并随后在其细胞内结构域上相互磷酸化。然而,越来越多的证据表明,受体寡聚化不仅仅是配体结合的结果,而是负责调节受体激活的复杂过程的一部分。重要的是,这些受体的寡聚化动力学及其随后的激活受到其他细胞成分的影响,例如细胞骨架机械和细胞膜脂质特性。因此,受体激活不是由配体-受体相互作用介导的孤立分子事件,而是涉及受体与其他细胞成分之间的协调相互作用。在活细胞上测量受体寡聚化动力学可以深入了解这些相互作用的特性。因此,开发能够以最佳时间和空间分辨率探测质膜上受体运动的技术至关重要。为此,已经使用了各种微观技术。光学技术,包括单分子跟踪 (SMT) 和荧光相关光谱 (FCS),测量活细胞上的受体扩散。通过检测荧光标记的受体之间的Förster 共振能量转移 (FRET) 或通过计数荧光点内的受体数量(逐步漂白),也可以评估受体-受体相互作用。本文将描述用于研究活细胞上受体寡聚化的光学技术的最新进展。这篇文章是由 Kalina Hristova 编辑的题为“细胞膜中膜受体之间的相互作用”的特刊的一部分。

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