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灯光、细胞骨架、行动:光遗传学控制细胞动力学。

Lights, cytoskeleton, action: Optogenetic control of cell dynamics.

机构信息

Department of Cell & Tissue Biology, University of California San Francisco, 513 Parnassus Avenue, San Francisco, CA 94143, USA.

Department of Cell & Tissue Biology, University of California San Francisco, 513 Parnassus Avenue, San Francisco, CA 94143, USA.

出版信息

Curr Opin Cell Biol. 2020 Oct;66:1-10. doi: 10.1016/j.ceb.2020.03.003. Epub 2020 May 1.

Abstract

Cell biology is moving from observing molecules to controlling them in real time, a critical step towards a mechanistic understanding of how cells work. Initially developed from light-gated ion channels to control neuron activity, optogenetics now describes any genetically encoded protein system designed to accomplish specific light-mediated tasks. Recent photosensitive switches use many ingenious designs that bring spatial and temporal control within reach for almost any protein or pathway of interest. This next generation optogenetics includes light-controlled protein-protein interactions and shape-shifting photosensors, which in combination with live microscopy enable acute modulation and analysis of dynamic protein functions in living cells. We provide a brief overview of various types of optogenetic switches. We then discuss how diverse approaches have been used to control cytoskeleton dynamics with light through Rho GTPase signaling, microtubule and actin assembly, mitotic spindle positioning and intracellular transport and highlight advantages and limitations of different experimental strategies.

摘要

细胞生物学正在从观察分子转变为实时控制分子,这是深入了解细胞工作机制的关键一步。光遗传学最初是从光门控离子通道发展而来,用于控制神经元活动,现在它描述了任何经过基因编码的蛋白系统,旨在完成特定的光介导任务。最近的光敏开关采用了许多巧妙的设计,使几乎任何感兴趣的蛋白或通路都能够实现空间和时间控制。这种新一代的光遗传学包括光控蛋白-蛋白相互作用和形状转变光传感器,与活细胞显微镜结合使用,可以在活细胞中急性调节和分析动态蛋白功能。我们简要概述了各种类型的光遗传学开关。然后,我们讨论了如何通过 Rho GTP 酶信号、微管和肌动蛋白组装、有丝分裂纺锤体定位和细胞内运输来用光控制细胞骨架动力学,并强调了不同实验策略的优点和局限性。

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