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基于荧光共振能量转移(FRET)的探针用于信号转导级联反应的体内成像。

In vivo imaging of signal transduction cascades with probes based on Förster Resonance Energy Transfer (FRET).

作者信息

Nakamura Takeshi, Matsuda Michiyuki

机构信息

Laboratory of Bioimaging and Cell Signaling, Graduate School of Biostudies, Kyoto University, Kyoto, Japan.

出版信息

Curr Protoc Cell Biol. 2009 Dec;Chapter 14:Unit 14.10. doi: 10.1002/0471143030.cb1410s45.

Abstract

Genetically encoded FRET probes enable us to visualize a variety of signaling events such as protein phosphorylation and G-protein activation in living cells. This unit focuses on FRET probes wherein both the donor and acceptor are fluorescence proteins and incorporated into a single molecule, i.e., a unimolecular probe. Advantages of these probes lie in their easy loading into cells, simple acquisition of FRET images, and clear evaluation of data. We have developed FRET probes for Ras-superfamily GTPases, designated Ras and interacting protein chimeric unit (Raichu) probes. We hereby describe strategies to develop Raichu-type FRET probes, procedures for their characterization, and acquisition and processing of images. Although improvements upon FRET probes are still based on trial-and-error, we provide practical tips for their optimization and briefly discuss the theory and applications of unimolecular FRET probes.

摘要

基因编码的荧光共振能量转移(FRET)探针使我们能够在活细胞中可视化各种信号事件,如蛋白质磷酸化和G蛋白激活。本单元重点介绍供体和受体均为荧光蛋白并整合到单个分子中的FRET探针,即单分子探针。这些探针的优点在于易于导入细胞、FRET图像采集简单以及数据评估清晰。我们开发了用于Ras超家族GTP酶的FRET探针,称为Ras与相互作用蛋白嵌合单元(Raichu)探针。在此,我们描述开发Raichu型FRET探针的策略、其表征程序以及图像采集和处理方法。尽管FRET探针的改进仍基于反复试验,但我们提供了优化它们的实用技巧,并简要讨论了单分子FRET探针的理论和应用。

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