首页> 外文期刊>Analytical Biochemistry: An International Journal of Analytical and Preparative Methods >Online nanoliquid chromatography-mass spectrometry and nanofluorescence detection for high-resolution quantitative N-glycan analysis
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Online nanoliquid chromatography-mass spectrometry and nanofluorescence detection for high-resolution quantitative N-glycan analysis

机译:在线纳米液相色谱-质谱联用和纳米荧光检测,用于高分辨率定量N-聚糖分析

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The characterization of the repertoire of glycans at the quantitative and qualitative levels on cells and glycoproteins is a necessary step to the understanding of glycan functions in biology. In addition, there is an increasing demand in the field of biotechnology for the monitoring of glycosylation of recombinant glycoproteins, an important issue with regard to their safety and biological activity. The enzymatic release followed by fluorescent derivatization of glycans and separation by normal phase high-performance liquid chromatography (HPLC) has proven for many years to be a powerful approach to the quantification of glycans. Characterization of glycans has classically been performed by mass spectrometry (MS) with external standardization. Here, we report a new method for the simultaneous quantification and characterization of the N-glycans on glycoproteins without the need for external standardization. This method, which we call glycan nanoprofiling, uses nanoLC-coupled electrospray ionization (ESI)-MS with an intercalated nanofluorescence reader and provides effective single glycan separation with subpicomolar sensitivity. The method relies on the isolation and coumaric derivatization of enzymatically released glycans collected by solid phase extraction with porous graphitized carbon and their separation over polyamide-based nanoHPLC prior to serial nanofluorescence and nanoelectrospray mass spectrometric analysis. Glycan nanoprofiling is a broadly applicable and powerful approach that is sufficient to identify and quantify many glycan oligomers in a single run. Glycan nanoprofiling was successfully applied to resolve the glycans of monoclonal antibodies, showing that this method is a fast and sensitive alternative to available methods.
机译:在细胞和糖蛋白的定量和定性水平上表征聚糖库是了解生物学中聚糖功能的必要步骤。另外,在生物技术领域中,对于监测重组糖蛋白的糖基化的需求日益增加,这是关于其安全性和生物活性的重要问题。多年以来,酶的释放,聚糖的荧光衍生化以及正相高效液相色谱(HPLC)的分离已被证明是量化聚糖的有效方法。聚糖的表征经典地通过具有外部标准化的质谱(MS)来进行。在这里,我们报告了一种新的方法,可以同时量化和表征糖蛋白上的N-聚糖,而无需外部标准化。这种方法,我们称为聚糖纳米轮廓分析,结合了纳米LC耦合电喷雾电离(ESI)-MS和插层式纳米荧光读取器,可提供亚皮摩尔级灵敏度的有效单聚糖分离。该方法依赖于通过多孔石墨化碳的固相萃取收集的酶促释放的聚糖的分离和香豆衍生化,以及在进行连续纳米荧光和纳米电喷雾质谱分析之前,通过聚酰胺基纳米HPLC对其进行分离。聚糖纳米轮廓分析是一种广泛适用且功能强大的方法,足以在一次运行中鉴定和定量许多聚糖低聚物。聚糖纳米轮廓分析已成功应用于解析单克隆抗体的聚糖,表明该方法是现有方法的快速,敏感的替代方法。

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