Literature DB >> 20013753

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

Takeshi Nakamura1, Michiyuki Matsuda.   

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.

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Year:  2009        PMID: 20013753     DOI: 10.1002/0471143030.cb1410s45

Source DB:  PubMed          Journal:  Curr Protoc Cell Biol        ISSN: 1934-2616


  2 in total

1.  Plexins are GTPase-activating proteins for Rap and are activated by induced dimerization.

Authors:  Yuxiao Wang; Huawei He; Nishi Srivastava; Sheikh Vikarunnessa; Yong-bin Chen; Jin Jiang; Christopher W Cowan; Xuewu Zhang
Journal:  Sci Signal       Date:  2012-01-17       Impact factor: 8.192

2.  Phosphorylation of STEF/Tiam2 by protein kinase A is critical for Rac1 activation and neurite outgrowth in dibutyryl cAMP-treated PC12D cells.

Authors:  Akihiro Goto; Mikio Hoshino; Michiyuki Matsuda; Takeshi Nakamura
Journal:  Mol Biol Cell       Date:  2011-04-01       Impact factor: 4.138

  2 in total

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