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一种适用于细胞外囊泡蛋白质组学分析的基于聚乙二醇的工作流程。

An Adaptable Polyethylene Glycol-Based Workflow for Proteomic Analysis of Extracellular Vesicles.

作者信息

Hurwitz Stephanie N, Meckes David G

机构信息

Department of Biomedical Sciences, Florida State University College of Medicine, 1115 West Call Street, Tallahassee, FL, 32306, USA.

出版信息

Methods Mol Biol. 2017;1660:303-317. doi: 10.1007/978-1-4939-7253-1_25.

Abstract

Extracellular vesicles (EVs), including exosomes are endocytically derived nanovesicles expelled from cells that contain molecular information in the form of lipids, proteins, and nucleic acids. Transfer of this information to other cells in local or distant microenvironments facilitates cell-to-cell communication. Importantly, diseased cells release exosomes containing specific cargo that may contribute to pathology and can be harnessed for diagnostic or prognostic use. The broad potential medical utility of exosomes has fueled rapidly expanding research on understanding the composition and functions of exosomes in normal and pathological conditions. Here, we provide a complete workflow for purifying exosome-sized vesicles from biological fluids for in-depth proteomic analyses. Moreover, this polyethylene glycol-based method is efficient, highly adaptable, and compatible with a variety of downstream applications.

摘要

细胞外囊泡(EVs),包括外泌体,是通过内吞作用从细胞中排出的纳米囊泡,其包含脂质、蛋白质和核酸形式的分子信息。将这些信息传递到局部或远处微环境中的其他细胞有助于细胞间通讯。重要的是,患病细胞会释放含有特定货物的外泌体,这些外泌体可能导致病理变化,并且可用于诊断或预后。外泌体广泛的潜在医学用途推动了对正常和病理条件下外泌体组成和功能的研究迅速扩展。在这里,我们提供了一种从生物流体中纯化外泌体大小囊泡以进行深入蛋白质组学分析的完整工作流程。此外,这种基于聚乙二醇的方法效率高、适应性强,并且与多种下游应用兼容。

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