Chemo-Enzymatic Synthesis of 13C Labeled Complex N-Glycans As Internal Standards for the Absolute Glycan Quantification by Mass Spectrometry

被引:39
作者
Echeverria, Begona [1 ]
Etxebarria, Juan [1 ]
Ruiz, Nerea [1 ]
Hernandez, Alvaro [1 ]
Calvo, Javier [2 ]
Haberger, Markus [3 ]
Reusch, Dietmar [3 ]
Reichardt, Niels-Christian [1 ,4 ]
机构
[1] CIC BiomaGUNE, Glycotechnol Grp, San Sebastian 20009, Spain
[2] CIC BiomaGUNE, Mass Spectrometry Platform, San Sebastian 20009, Spain
[3] Roche Diagnost GmbH, Pharma Biotech Dev Penzberg, D-82377 Penzberg, Germany
[4] CIBER Bioingn Biomat & Nanomed CIBER BBN, San Sebastian 20009, Spain
关键词
QUANTITATIVE-ANALYSIS; GLYCOSYLATION; IDENTIFICATION; FUCOSYLATION; STRATEGY; BLOOD; TAGS;
D O I
10.1021/acs.analchem.5b03135
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
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.
引用
收藏
页码:11460 / 11467
页数:8
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