Visualizing the Signal Transduction Pathways in Living Cells with GFP-Based FRET Probes
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- Kurokawa Kazuo
- Department of Tumor Virology, Research Institute for Microbial Diseases, Osaka University
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- Takaya Akiyuki
- Department of Tumor Virology, Research Institute for Microbial Diseases, Osaka University
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- Terai Kenta
- Department of Tumor Virology, Research Institute for Microbial Diseases, Osaka University
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- Fujioka Aki
- Department of Tumor Virology, Research Institute for Microbial Diseases, Osaka University
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- Matsuda Michiyuki
- Department of Tumor Virology, Research Institute for Microbial Diseases, Osaka University
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説明
Visualizing how signals are transmitted within a living cell has long been a goal of molecular biologists, which has now been realized by probes based on the principle of fluorescence resonance energy transfer (FRET). Variants of green fluorescent protein (GFP) enabled the preparation of genetically-encoded FRET probes, and their application has been expanded for use in many areas of biology. The GFP-based FRET probes can be classified as belonging to one of two types, intermolecular and intramolecular FRET probes. The merit of the intermolecular FRET probe lies in the ease of preparation of the probes, whereas the merit of the intramolecular FRET probe lies in the high signal-to-noise ratio. Although these GFP-based probes are powerful tools for the visualization of signal transduction cascades, numerous pitfalls remain associated with this technique. Here, we provide an overview of the GFP-based FRET probes and discuss these issues.<br>
収録刊行物
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- Acta Histochemica et Cytochemica
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Acta Histochemica et Cytochemica 37 (6), 347-355, 2004
日本組織細胞化学会
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詳細情報 詳細情報について
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- CRID
- 1390282679839383552
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- NII論文ID
- 110003161214
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- NII書誌ID
- AA00508022
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- ISSN
- 13475800
- 00445991
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- Crossref
- NDLデジコレ(旧NII-ELS)
- CiNii Articles
- OpenAIRE
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- 抄録ライセンスフラグ
- 使用不可