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Solubilization of human cells by the styrene-maleic acid copolymer: Insights from fluorescence microscopy

机译:通过苯乙烯 - 马来酸共聚物溶解人细胞:荧光显微镜的见解

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摘要

Extracting membrane proteins from biological membranes by styrene-maleic acid copolymers (SMAs) in the form of nanodiscs has developed into a powerful tool in membrane research. However, the mode of action of membrane (protein) solubilization in a cellular context is still poorly understood and potential specificity for cellular compartments has not been investigated. Here, we use fluorescence microscopy to visualize the process of SMA solubilization of human cells, exemplified by the immortalized human HeLa cell line. Using fluorescent protein fusion constructs that mark distinct subcellular compartments, we found that SMA solubilizes membranes in a concentration-dependent multi-stage process. While all major intracellular compartments were affected without a strong preference, plasma membrane solubilization was found to be generally slower than the solubilization of organelle membranes. Interestingly, some plasma membrane-localized proteins were more resistant against solubilization than others, which might be explained by their presence in specific membrane domains with differing properties. Our results support the general applicability of SMA for the isolation of membrane proteins from different types of (sub)cellular membranes.
机译:用苯乙烯 - 马来酸共聚物(SMA)从生物膜中提取膜蛋白,以纳米DISCS的形式开发成膜研究的强大工具。然而,膜(蛋白质)溶解在细胞上下文中的作用方式仍然是较差的,并且尚未研究细胞室的潜在特异性。在此,我们使用荧光显微镜观察人细胞的SMA溶解的过程,示例于永生化的人Hela细胞系。使用标记不同亚细胞室的荧光蛋白融合构建体,我们发现SMA溶解在浓度依赖性的多级过程中的膜。虽然所有主要的细胞内隔室都受到强烈偏好的影响,但发现血浆膜溶解通常比细胞器膜的溶解较慢。有趣的是,一些血浆膜局部化蛋白质比其他溶解更耐溶解,其可以通过它们在特定膜结构域中的存在来解释具有不同性质的。我们的研究结果支持SMA的一般适用性,用于从不同类型(亚)细胞膜中的膜蛋白分离。

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