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{"title":"Protein-Lipid Interaction by Fluorescence (PLIF) to Characterize and Screen for Inhibitors of Protein-Phosphoinositide Interactions","authors":"Laurie Ceccato, Mélanie Mansat, Bernard Payrastre, Frédérique Gaits-Iacovoni, Julien Viaud","doi":"10.1002/cpps.35","DOIUrl":null,"url":null,"abstract":"<p>Phosphoinositides are key signaling and regulatory phospholipids that mediate important pathophysiological processes. This is achieved through the interaction of their phosphorylated inositol head group with a wide range of protein domains. Therefore, being able to determine the phosphoinositide specificity for effector protein is essential to the understanding of its cellular function. This unit describes a novel method named Protein-Lipid Interaction by Fluorescence, or PLIF. PLIF is a fast, reliable and high throughput assay that allows determination of the phosphoinositide specificity of proteins, simultaneously providing relative affinities. In addition, PLIF is suitable for screening inhibitors of protein- phosphoinositide interaction, allowing identification of potential pharmacological compounds. © 2017 by John Wiley & Sons, Inc.</p>","PeriodicalId":10866,"journal":{"name":"Current Protocols in Protein Science","volume":"89 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-02-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpps.35","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Protein Science","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cpps.35","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
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Abstract
Phosphoinositides are key signaling and regulatory phospholipids that mediate important pathophysiological processes. This is achieved through the interaction of their phosphorylated inositol head group with a wide range of protein domains. Therefore, being able to determine the phosphoinositide specificity for effector protein is essential to the understanding of its cellular function. This unit describes a novel method named Protein-Lipid Interaction by Fluorescence, or PLIF. PLIF is a fast, reliable and high throughput assay that allows determination of the phosphoinositide specificity of proteins, simultaneously providing relative affinities. In addition, PLIF is suitable for screening inhibitors of protein- phosphoinositide interaction, allowing identification of potential pharmacological compounds. © 2017 by John Wiley & Sons, Inc.
蛋白-脂质相互作用荧光(PLIF)表征和筛选蛋白-磷酸肌苷相互作用抑制剂
磷酸肌苷是介导重要病理生理过程的关键信号和调节磷脂。这是通过它们磷酸化的肌醇头部组与广泛的蛋白质结构域的相互作用实现的。因此,能够确定效应蛋白的磷酸肌肽特异性对了解其细胞功能至关重要。本单元描述了一种名为荧光蛋白-脂质相互作用或PLIF的新方法。PLIF是一种快速、可靠和高通量的检测方法,可以测定蛋白质的磷酸肌肽特异性,同时提供相对亲和力。此外,PLIF适用于筛选蛋白质-磷酸肌苷相互作用抑制剂,从而鉴定潜在的药理化合物。©2017 by John Wiley &儿子,Inc。
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