基于 ORP9-PH 结构域的荧光报告器,用于观察活细胞中磷脂酰肌醇-4-磷酸的动态变化

IF 4.2 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Moeka Ajiki, Masaru Yoshikawa, Tomoki Miyazaki, Asami Kawasaki, Kazuhiro Aoki, Fubito Nakatsu and Shinya Tsukiji
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引用次数: 0

摘要

在活细胞中可视化磷脂酰肌醇 4-磷酸(PI4P)的荧光报告物对于阐明这种基本脂质在细胞生理学中的作用不可或缺。然而,目前可用的 PI4P 报告存在局限性,如偏向高尔基体定位和检测灵敏度低。在这里,我们展示了一系列基于氧固醇结合蛋白相关蛋白 9(ORP9)的褶皱同源(PH)结构域的 PI4P 荧光报告物。我们发现,绿色荧光蛋白 AcGFP1 标记的 ORP9-PH 结构域可用作荧光 PI4P 报告物,以高特异性和高对比度检测细胞 PI4P 在多个细胞位置的广泛分布,包括质膜(PM)、高尔基体、内体和溶酶体。我们还开发了适用于多色荧光成像实验的蓝色、红色和近红外荧光 PI4P 报告物。最后,我们展示了基于 ORP9-PH 结构域的报告物在合成 ER-PM 膜接触操作和 GPCR 刺激下可视化活细胞中 PI4P 分布和水平动态变化的实用性。这项工作提供了一组新的基因编码荧光 PI4P 报告物,可用于 PI4P 生物学研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

ORP9-PH domain-based fluorescent reporters for visualizing phosphatidylinositol 4-phosphate dynamics in living cells†

ORP9-PH domain-based fluorescent reporters for visualizing phosphatidylinositol 4-phosphate dynamics in living cells†

ORP9-PH domain-based fluorescent reporters for visualizing phosphatidylinositol 4-phosphate dynamics in living cells†

Fluorescent reporters that visualize phosphatidylinositol 4-phosphate (PI4P) in living cells are indispensable to elucidate the roles of this fundamental lipid in cell physiology. However, currently available PI4P reporters have limitations, such as Golgi-biased localization and low detection sensitivity. Here, we present a series of fluorescent PI4P reporters based on the pleckstrin homology (PH) domain of oxysterol-binding protein-related protein 9 (ORP9). We show that the green fluorescent protein AcGFP1-tagged ORP9-PH domain can be used as a fluorescent PI4P reporter to detect cellular PI4P across its wide distribution at multiple cellular locations, including the plasma membrane (PM), Golgi, endosomes, and lysosomes with high specificity and contrast. We also developed blue, red, and near-infrared fluorescent PI4P reporters suitable for multicolor fluorescence imaging experiments. Finally, we demonstrate the utility of the ORP9-PH domain-based reporter to visualize dynamic changes in the PI4P distribution and level in living cells upon synthetic ER–PM membrane contact manipulation and GPCR stimulation. This work offers a new set of genetically encoded fluorescent PI4P reporters that are practically useful for the study of PI4P biology.

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来源期刊
CiteScore
6.10
自引率
0.00%
发文量
128
审稿时长
10 weeks
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