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使用脱氧胆酸钠洗涤剂增强定量 LC-MS/MS 分析糖蛋白衍生的 N-连接聚糖。

Enhanced Quantitative LC-MS/MS Analysis of N-linked Glycans Derived from Glycoproteins Using Sodium Deoxycholate Detergent.

机构信息

Department of Chemistry and Biochemistry , Texas Tech University , Lubbock , Texas 79409 , United States.

出版信息

J Proteome Res. 2018 Aug 3;17(8):2668-2678. doi: 10.1021/acs.jproteome.8b00127. Epub 2018 Jul 20.

Abstract

Protein glycosylation is a common protein post-translational modification (PTM) in living organisms and has been shown to associate with multiple diseases, and thus may potentially be a biomarker of such diseases. Efficient protein/glycoprotein extraction is a crucial step in the preparation of N-glycans derived from glycoproteins prior to LC-MS analysis. Convenient, efficient and unbiased sample preparation protocols are needed. Herein, we evaluated the use of sodium deoxycholate (SDC) acidic labile detergent to release N-glycans of glycoproteins derived from biological samples such as cancer cell lines. Compared to the filter-aided sample preparation approach, the sodium deoxycholate (SDC) assisted approach was determined to be more efficient and unbiased. SDC removal was determined to be more efficient when using acidic precipitation rather than ethyl acetate phase transfer. Efficient extraction of proteins/glycoproteins from biological samples was achieved by combining SDC lysis buffer and beads beating cell disruption. This was suggested by a significant overall increase in the intensities of N-glycans released from cancer cell lines. Additionally, the use of SDC approach was also shown to be more reproducible than those methods that do not use SDC.

摘要

蛋白质糖基化是生物体内常见的蛋白质翻译后修饰(PTM),已被证明与多种疾病相关,因此可能是这些疾病的生物标志物。在 LC-MS 分析之前,从糖蛋白中衍生 N-糖链的过程中,高效的蛋白质/糖蛋白提取是准备工作的关键步骤。需要方便、高效且无偏倚的样品制备方案。在此,我们评估了使用脱氧胆酸钠(SDC)酸性不稳定去污剂释放来自生物样品(如癌细胞系)的糖蛋白衍生的 N-糖链。与过滤辅助样品制备方法相比,确定 SDC 辅助方法更有效且无偏倚。与乙酸乙酯相转移相比,酸性沉淀时 SDC 的去除效率更高。通过结合 SDC 裂解缓冲液和珠子剧烈搅拌细胞破碎,从生物样品中高效提取蛋白质/糖蛋白。这是通过从癌细胞系释放的 N-糖链的强度显著增加来证明的。此外,与不使用 SDC 的方法相比,SDC 方法的重现性也更好。

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