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首页> 外文期刊>Analytical chemistry >Chemo-Enzymatic Synthesis of C-13 Labeled Complex N-Glycans As Internal Standards for the Absolute Glycan Quantification by Mass Spectrometry
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Chemo-Enzymatic Synthesis of C-13 Labeled Complex N-Glycans As Internal Standards for the Absolute Glycan Quantification by Mass Spectrometry

机译:化学-酶法合成C-13标记的复杂N-聚糖作为内标的质谱定量法

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摘要

Methods for the absolute quantification of glycans are needed in glycoproteomics, during development and production of biopharmaceuticals and for the clinical analysis of glycan disease markers. Here we present a strategy for the chemo-enzymatic synthesis of C-13 labeled N-glycan libraries and provide an example for their use as internal standards in the profiling and absolute quantification of mAb glycans by matrix-assisted laser desorption ionization-time-of-flight (MALDI-TOF) mass spectrometry. A synthetic biantennary glycan precursor was C-13-labeled on all four amino sugar residues and enzymatically derivatized to produce a library of 15 glycan isotopologues with a mass increment of 8 Da over the natural products. Asymmetrically elongated glycans were accessible by performing enzymatic reactions on partially protected UV-absorbing intermediates, subsequent fractionation by preparative HPLC, and final hydrogenation. Using a preformulated mixture of eight internal standards, we quantified the glycans in a monoclonal therapeutic antibody with excellent precision and speed.
机译:在糖蛋白组学中,生物药物的开发和生产过程中以及糖类疾病标志物的临床分析中,需要用于糖类绝对定量的方法。在这里,我们介绍了化学酶促合成C-13标记的N-聚糖文库的策略,并提供了一个实例,供它们用作通过基质辅助激光解吸电离-时间-质谱分析和绝对定量mAb聚糖的内标物飞行(MALDI-TOF)质谱。将合成的双触角聚糖前体在所有四个氨基糖残基上进行C-13标记,然后酶促衍生,以生成15个聚糖同位素同质物的文库,其天然产物的质量增量为8 Da。通过在部分受保护的吸收紫外线的中间体上进行酶促反应,随后通过制备型HPLC进行分馏以及最终氢化,可实现不对称加长的聚糖。使用八个内部标准液的预配制混合物,我们以优异的精确度和速度对单克隆治疗性抗体中的聚糖进行了定量。

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