Gregor P. Jose, Thomas J. Pucadyil
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Abstract
Peripheral membrane proteins participate in numerous biological pathways. Thus, methods to analyze their membrane-binding characteristics have become important. In this report, we detail protocols for the synthesis and utilization of a photoactivable fluorescent lipid as a reporter to monitor membrane binding of proteins. The assay, referred to as proximity-based labeling of membrane-associated proteins (PLiMAP), is based on UV activation of a fluorescent lipid reporter, which in turn crosslinks with proteins bound to membranes and renders them fluorescent. © 2020 Wiley Periodicals LLC.
Basic Protocol 1 : Synthesis of BODIPY-diazirine phosphatidylethanolamine (BDPE)
Basic Protocol 2 : Preparation of BDPE-containing liposomes
Basic Protocol 3 : Performing PLiMAP with a candidate protein
Basic Protocol 4 : Quantitation of liposome-binding properties of the candidate protein from analyzing in-gel fluorescence
Support Protocol : Purification of GST-2×P4M domain of SidM protein
PLiMAP:基于接近度的膜相关蛋白标记
外周膜蛋白参与多种生物学途径。因此,分析其膜结合特性的方法变得非常重要。在本报告中,我们详细介绍了一种光活化荧光脂质的合成和利用方案,作为监测蛋白质膜结合的报告。该检测被称为基于接近度的膜相关蛋白标记(PLiMAP),是基于紫外线激活的荧光脂质报告蛋白,该报告蛋白反过来与结合在膜上的蛋白质交联并使其荧光。©2020 Wiley期刊公司。基本方案1:合成bodipy -二嗪磷脂酰乙醇胺(BDPE)基本方案2:制备含BDPE的脂质体基本方案3:用候选蛋白进行PLiMAP基本方案4:通过分析凝胶内荧光定量候选蛋白的脂质体结合特性支持方案:纯化SidM蛋白的GST-2×P4M结构域
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