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免疫荧光标记脂结合蛋白 CERTs 以监测脂筏动力学。

Immunofluorescence Labeling of Lipid-Binding Proteins CERTs to Monitor Lipid Raft Dynamics.

机构信息

Division of Neuroscience, School for Mental Health and Neuroscience, Maastricht University, Maastricht, The Netherlands.

Department of Physiology, University of Kentucky College of Medicine, Lexington, KY, USA.

出版信息

Methods Mol Biol. 2021;2187:327-335. doi: 10.1007/978-1-0716-0814-2_19.

Abstract

Fluorescence microscopy is a powerful and widely used tool in molecular biology. Over the years, the discovery and development of lipid-binding fluorescent probes has established new research possibilities to investigate lipid composition and dynamics in the cell. For instance, fluorescence microscopy has allowed the investigation of lipid localization and density in specific cell compartments such as membranes or organelles. Often, the characteristics and the composition of lipid-enriched structures are determined by analyzing the distribution of a fluorescently labeled lipid probe, which intercalates in lipid-enriched platforms, or specifically binds to parts of the lipid molecule. However, in many cases antibodies targeting proteins have higher specificity and are easier to generate. Therefore, we propose to use both antibodies targeting lipid transporters and lipid binding probes to better monitor lipid membrane changes. As an example, we visualize lipid rafts using the fluorescently labeled-B-subunit of the cholera toxin in combination with antibodies targeting ceramide-binding proteins CERTs, central molecules in the metabolism of sphingolipids.

摘要

荧光显微镜是分子生物学中一种强大且广泛应用的工具。多年来,脂质结合荧光探针的发现和发展为研究细胞内脂质组成和动态提供了新的研究可能性。例如,荧光显微镜已允许研究特定细胞区室(如膜或细胞器)中脂质的定位和密度。通常,通过分析荧光标记脂质探针的分布来确定富含脂质的结构的特征和组成,该探针插入富含脂质的平台中,或特异性结合脂质分子的部分。然而,在许多情况下,针对蛋白质的抗体具有更高的特异性,并且更容易生成。因此,我们建议同时使用针对脂质转运蛋白和脂质结合探针的抗体,以更好地监测脂质膜的变化。例如,我们使用霍乱毒素的 B 亚单位荧光标记物与针对神经酰胺结合蛋白 CERT 的抗体结合,可视化脂质筏,CERT 是神经鞘脂代谢中的核心分子。

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