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教学资源。利用荧光蛋白对活细胞中的成像信号转导进行研究。

Teaching resources. Imaging signal transduction in living cells with fluorescent proteins.

作者信息

Philips Mark R

机构信息

Department of Medicine, New York University School of Medicine, New York, NY 10016, USA.

出版信息

Sci STKE. 2005 Dec 13;2005(314):tr28. doi: 10.1126/stke.3142005tr28.

Abstract

Until recently, studies in this field of signal transduction have involved the "what" and "when" of signaling. Who talks to whom and for how long? With the advent of genetically encoded fluorescent proteins, it has become possible to monitor signaling events in living cells in real time. This has added the dimension of "where" to the study of cellular signaling. This lecture, which is a part of "Cell Signaling Systems: A Course for Graduate Students," provides a survey of how green fluorescent protein (GFP)-tagged probes for signaling events have been used to elucidate new pathways, to describe the kinetics of signaling events at the single-cell level, and to reveal upon which subcellular compartments these events take place. Some of the findings confirm previous ones using biochemical techniques, and others have been surprising. Examples include those utilizing protein localization, relocalization, fluorescence recovery after photobleaching (FRAP), and fluorescence resonance energy transfer (FRET). The design of FRET probes is described. The detection of small guanosine triphosphatase (GTPase) signaling in living cells is used as an example to explore the creative and diverse ways investigators have developed to look at this system.

摘要

直到最近,该信号转导领域的研究还主要围绕信号传导的“是什么”和“何时发生”。谁与谁进行交流,交流持续多长时间?随着基因编码荧光蛋白的出现,实时监测活细胞中的信号传导事件成为可能。这为细胞信号传导研究增添了“何处发生”这一方面。本次讲座是“细胞信号系统:研究生课程”的一部分,它概述了用于信号传导事件的绿色荧光蛋白(GFP)标记探针如何被用于阐明新的信号通路、描述单细胞水平信号传导事件的动力学,以及揭示这些事件发生在哪些亚细胞区室。一些研究结果证实了之前使用生化技术得到的结果,而另一些则令人惊讶。实例包括那些利用蛋白质定位、重新定位、光漂白后荧光恢复(FRAP)以及荧光共振能量转移(FRET)的研究。文中还描述了FRET探针的设计。以活细胞中小GTP酶信号传导的检测为例,探讨了研究人员为研究该系统所开发的创新且多样的方法。

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