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通过密度梯度离心法分离内吞细胞器。

Isolation of endocitic organelles by density gradient centrifugation.

作者信息

de Araùjo Mariana Eça Guimarães, Huber Lukas Alfons, Stasyk Taras

出版信息

Methods Mol Biol. 2008;424:317-31. doi: 10.1007/978-1-60327-064-9_25.

Abstract

Advanced prefractionation strategies, in combination with highly sensitive and accurate mass spectrometers provide powerful means to detect and analyze low abundant proteins on the subcellular and organelle-specific level. Among enrichment techniques, subcellular fractionation has become the most commonly used. Its application gives access to less complex subproteomes and organelle constituents, facilitating downstream analysis. Furthermore, subcellular fractionation allows the identification of proteins that shuttle between different subcellular compartments in a stimulus dependent manner. As a paradigm of subcellular organelle isolation, we describe here endosomal purification protocols, based on differential centrifugation in continuous and discontinuous sucrose gradients. Described methods can be easily modified to isolate other organelles and are compatible with subsequent organelle- and functional organelle proteome analyses by, e.g., two-dimensional gel electrophoresis.

摘要

先进的预分级策略与高灵敏度和高精度的质谱仪相结合,为在亚细胞和细胞器特异性水平上检测和分析低丰度蛋白质提供了强大手段。在富集技术中,亚细胞分级分离已成为最常用的方法。其应用能够获取复杂度较低的亚蛋白质组和细胞器成分,便于下游分析。此外,亚细胞分级分离还能鉴定以刺激依赖方式在不同亚细胞区室之间穿梭的蛋白质。作为亚细胞器分离的范例,我们在此描述基于连续和不连续蔗糖梯度差速离心的内体纯化方案。所描述的方法可轻松修改以分离其他细胞器,并且与随后通过例如二维凝胶电泳进行的细胞器和功能性细胞器蛋白质组分析兼容。

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