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一种实用的方法,用 9-芴甲氧羰基衍生物制备荧光标记的聚糖,以简化基于荧光 HPLC 的分析。

A practical method for preparing fluorescent-labeled glycans with a 9-fluorenylmethyl derivative to simplify a fluorimetric HPLC-based analysis.

机构信息

Department of Pharmaceutical Sciences, Kindai University, Kowakae 3-4-1, Higashi-osaka 577-8502, Japan.

Department of Pharmaceutical Sciences, Kindai University, Kowakae 3-4-1, Higashi-osaka 577-8502, Japan.

出版信息

J Pharm Biomed Anal. 2020 Jul 15;186:113267. doi: 10.1016/j.jpba.2020.113267. Epub 2020 Mar 20.

Abstract

Analysis of glycans in glycoproteins is often performed by liquid chromatography (LC) separation coupled with fluorescence detection and/or mass spectrometric detection. Enzymatically or chemically released glycans from glycoproteins are usually labeled by reductive amination with a fluorophore reagent. Although labeling techniques based on reductive amination have been well-established as sample preparation methods for fluorometric HPLC-based glycan analysis, they often include time-consuming and tedious purification steps. Here, we reported an alternative fluorescent labeling method based on the synthesis of hydrazone and its reduction using 9-fluorenylmethyl carbazate (Fmoc-hydrazine) as a fluorophore reagent. Using isomaltopentaose and N-glycans from human IgG, we optimized the Fmoc-labeling conditions and purification procedure of Fmoc-labeled N-glycans and applied the optimized method for the analysis of N-glycans released from four glycoproteins (bovine RNase B, human fibrinogen, human α1-acid glycoprotein, and bovine fetuin). The complete workflow for preparation of fluorescent-labeled N-glycans takes a total of 3.5 h and is simple to implement. The method presented here lowers the overall cost of a fluorescently labeled N-glycan and will be practically useful for the screening of disease-related glycans or routine analysis at an early stage of development of biopharmaceuticals.

摘要

糖蛋白中的聚糖分析通常通过液相色谱(LC)分离与荧光检测和/或质谱检测相结合来进行。糖蛋白中经酶解或化学法释放的聚糖通常通过与荧光团试剂的还原胺化进行标记。尽管基于还原胺化的标记技术已被很好地确立为基于荧光 HPLC 的聚糖分析的样品制备方法,但它们通常包括耗时且繁琐的纯化步骤。在这里,我们报告了一种替代的荧光标记方法,该方法基于腙的合成及其使用 9-芴基甲氧基羰酰基(Fmoc-肼)作为荧光团试剂的还原。使用异麦芽五糖和人 IgG 的 N-聚糖,我们优化了 Fmoc-标记 N-聚糖的 Fmoc-标记条件和纯化程序,并将优化后的方法应用于从四种糖蛋白(牛核糖核酸酶 B、人纤维蛋白原、人α1-酸性糖蛋白和牛胎球蛋白)中释放的 N-聚糖的分析。荧光标记 N-聚糖的完整工作流程总共需要 3.5 小时,实施简单。本文提出的方法降低了荧光标记 N-聚糖的总成本,对于筛选与疾病相关的聚糖或在生物制药开发的早期阶段进行常规分析将具有实际意义。

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