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利用锌指核酸酶基因靶向技术对人类细胞系进行糖基工程改造:具有均一的N-乙酰半乳糖胺O-糖基化的简单细胞可通过一步凝集素亲和层析分离O-糖蛋白组。

Glycoengineering of human cell lines using zinc finger nuclease gene targeting: SimpleCells with homogeneous GalNAc O-glycosylation allow isolation of the O-glycoproteome by one-step lectin affinity chromatography.

作者信息

Steentoft Catharina, Bennett Eric Paul, Clausen Henrik

机构信息

Department of Cellular and Molecular Medicine, Copenhagen Center for Glycomics, University of Copenhagen, Copenhagen N, Denmark.

出版信息

Methods Mol Biol. 2013;1022:387-402. doi: 10.1007/978-1-62703-465-4_29.

Abstract

Lectin affinity chromatography is a powerful technique for isolation of glycoproteins carrying a specific glycan structure of interest. However, the enormous diversity of glycans present on the cell surface, as well as on individual proteins, makes it difficult to isolate an entire glycoproteome with one or even a series of lectins. Here we present a technique to generate cell lines with homogenous truncated O-glycans using zinc finger nuclease gene targeting. Because of their simplified O-glycoproteome, the cells have been named SimpleCells. Glycoproteins from SimpleCells can be isolated in a single purification step by lectin chromatography performed on a long lectin column. This protocol describes Zinc finger nuclease gene targeting of human cells to simplify the glycoproteome, as well as lectin chromatography and isolation of glycopeptides from total cell lysates of SimpleCells.

摘要

凝集素亲和层析是一种用于分离携带特定目标聚糖结构的糖蛋白的强大技术。然而,细胞表面以及单个蛋白质上存在的聚糖种类繁多,使得使用一种甚至一系列凝集素分离整个糖蛋白组变得困难。在此,我们展示了一种利用锌指核酸酶基因靶向技术生成具有均匀截短O-聚糖的细胞系的方法。由于其简化的O-糖蛋白组,这些细胞被命名为SimpleCells。来自SimpleCells的糖蛋白可以通过在长凝集素柱上进行的凝集素层析在单个纯化步骤中分离出来。本方案描述了利用锌指核酸酶对人类细胞进行基因靶向以简化糖蛋白组,以及凝集素层析和从SimpleCells的总细胞裂解物中分离糖肽的方法。

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