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细胞中 Rac1 小 GTP 酶活性的可视化。

Visualization of the Activity of Rac1 Small GTPase in a Cell.

机构信息

Department of Pathology, Saitama Medical Center, Saitama Medical University, 1981 Kamoda, Kawagoe, Saitama 350-8550, Japan.

出版信息

Acta Histochem Cytochem. 2010 Dec 29;43(6):163-8. doi: 10.1267/ahc.10025. Epub 2010 Dec 23.

Abstract

Rho family G proteins including Rac regulate a variety of cellular functions, such as morphology, motility, and gene expression. Here we developed a fluorescence resonance energy transfer-based analysis in which we could monitor the activity of Rac1. To detect fluorescence resonance energy transfer, yellow fluorescent protein fused Rac1 and cyan fluorescent protein fused Cdc42-Rac1-interaction-binding domain of Pak1 protein were used as intermolecular probes of FRET. The fluorophores were separated with linear unmixing method. The fluorescence resonance energy transfer efficiency was measured by acceptor photobleaching assisted assay. With these methods, the Rac1 activity was visualized in a cell. The present findings indicate that this approach is sensitive enough to achieve results similar to those from ratiometric fluorescence resonance energy transfer analysis.

摘要

Rho 家族 G 蛋白(包括 Rac)调节多种细胞功能,如形态、运动和基因表达。在这里,我们开发了一种基于荧光共振能量转移的分析方法,用于监测 Rac1 的活性。为了检测荧光共振能量转移,我们使用融合了黄色荧光蛋白的 Rac1 和融合了 Pak1 蛋白的 CDC42-Rac1 相互作用结合域的青色荧光蛋白作为 FRET 的分子间探针。荧光团通过线性解混方法分离。荧光共振能量转移效率通过接受体光漂白辅助测定来测量。通过这些方法,可以在细胞中可视化 Rac1 的活性。本研究结果表明,这种方法足够灵敏,可以获得与比率荧光共振能量转移分析相似的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/386b/3015054/38beeae107b6/AHC10025f01.jpg

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