HILIC-UPLC-MS for high throughput and isomeric N-glycan separation and characterization in Congenital Disorders Glycosylation and human diseases
- 11 September 2020
- journal article
- research article
- Published by Springer Nature in Glycoconjugate Journal
- Vol. 38 (2) , 201-211
Abstract
N-glycan analyses may serve uncovering disease-associated biomarkers, as well as for profiling distinctive changes supporting diagnosis of genetic disorders of glycan biosynthesis named congenital disorders of glycosylation (CDG). Strategies based on liquid chromatography (LC) preferentially coupled to electrospray ionization (ESI) - mass spectrometry (MS) have emerged as powerful analytical methods for N-glycan identification and characterization. To enhance detection sensitivity, glycans are commonly labelled with a functional tag prior to LC-MS analysis. Since most derivatization techniques are notoriously time-consuming, some commercial analytical kits have been developed to speed up N-deglycosylation and N-glycan labelling of glycoproteins of pharmaceutical and biological interest such as monoclonal antibodies (mAbs). We exploited the analytical capabilities of RapiFluor-MS (RFMS) to perform, by a slightly modified protocol, a detailed N-glycan characterization of total serum and single serum glycoproteins from specific patients with CDG (MAN1B1-CDG, ALG12-CDG, MOGS-CDG, TMEM199-CDG). This strategy, accomplished by Hydrophilic Interaction Chromatography (HILIC)-UPLC-ESI-MS separation of the RFMS derivatized N-glycans, allowed us to uncover structural details of patients serum released N-glycans, thus extending the current knowledge on glycan profiles in these individual glycosylation diseases. The applied methodology enabled to differentiate in some cases either structural isomers and isomers differing in the linkage type. All the here reported applications demonstrated that RFMS method, coupled to HILIC-UPLC-ESI-MS, represents a sensitive high throughput approach for serum N-glycome analysis and a valuable option for glycan detection and separation particularly for isomeric species.Keywords
Funding Information
- Association Vaincre le Maladies Lysosomales (Agreement N ° 2018-5C)
This publication has 64 references indexed in Scilit:
- Targeted Biomarker Discovery by High Throughput Glycosylation Profiling of Human Plasma Alpha1-Antitrypsin and Immunoglobulin APLOS ONE, 2013
- Loci Associated with N-Glycosylation of Human Immunoglobulin G Show Pleiotropy with Autoimmune Diseases and Haematological CancersPLOS Genetics, 2013
- The impact of mass spectrometry in the diagnosis of congenital disorders of glycosylationJournal of Inherited Metabolic Disease, 2011
- Genomics Meets Glycomics—The First GWAS Study of Human N-Glycome Identifies HNF1α as a Master Regulator of Plasma Protein FucosylationPLOS Genetics, 2010
- The evaluation of a novel approach for the profiling and identification of N-linked glycan with a procainamide tag by HPLC with fluorescent and mass spectrometric detectionJournal of Pharmaceutical and Biomedical Analysis, 2010
- Improved Hydrophilic Interaction Chromatography LC/MS of Heparinoids Using a Chip with Postcolumn Makeup FlowAnalytical Chemistry, 2009
- A chip‐based amide‐HILIC LC/MS platform for glycosaminoglycan glycomics profilingProteomics, 2009
- Long‐standing mild hypertransaminasaemia caused by congenital disorder of glycosylation (CDG) type IIxJournal of Inherited Metabolic Disease, 2008
- Molecular and clinical description of the first US patients with congenital disorder of glycosylation IgMolecular Genetics and Metabolism, 2005
- Congenital Disorders of Glycosylation Type Ig Is Defined by a Deficiency in Dolichyl-P-mannose:Man7GlcNAc2-PP-dolichyl MannosyltransferaseJournal of Biological Chemistry, 2002