4.5 Article

High-throughput and high-sensitivity N-Glycan profiling: A platform for biopharmaceutical development and disease biomarker discovery

期刊

ANALYTICAL BIOCHEMISTRY
卷 623, 期 -, 页码 -

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ab.2021.114205

关键词

Glycosylation; Glycomics; Glycan profiling; Antibody; Human serum; Biomarker discovery; HILIC-FLD; Exoglycosidase

资金

  1. Science Foundation Ireland/Enterprise Ireland Technology Innovation Development Award [18/TIDA/6064]
  2. Science Foundation Ireland (SFI) [18/TIDA/6064] Funding Source: Science Foundation Ireland (SFI)

向作者/读者索取更多资源

This study presents an improved 96-well plate format platform for streamlined glycan profiling, allowing high sensitivity and high-throughput identification and quantification of diverse N-glycans. The technology offers a powerful tool for rapid advancement in glycan analysis for biopharmaceutical development and biomarker discovery in clinical disease diagnosis.
Protein glycosylation contributes to critical biological function of glycoproteins. Glycan analysis is essential for the production of biopharmaceuticals as well as for the identification of disease biomarkers. However, glycans are highly heterogeneous, which has considerably hampered the progress of glycomics. Here, we present an improved 96-well plate format platform for streamlined glycan profiling that takes advantage of rapid glycoprotein denaturation, deglycosylation, fluorescent derivatization, and on-matrix glycan clean-up. This approach offers high sensitivity with consistent identification and quantification of diverse N-glycans across multiple samples on a high-throughput scale. We demonstrate its capability for N-glycan profiling of glycoproteins from various sources, including two recombinant monoclonal antibodies produced from Chinese Hamster Ovary cells, EG2-hFc and rituximab, polyclonal antibodies purified from human serum, and total glycoproteins from human serum. Combined with the complementary information obtained by sequential digestion from exoglycosidase arrays, this approach allows the detection and identification of multiple N-glycans in these complex biological samples. The reagents, workflow, and Hydrophilic interaction liquid chromatography with fluorescence detection (HILIC-FLD), are simple enough to be implemented into a straightforward user-friendly setup. This improved technology provides a powerful tool in support of rapid advancement of glycan analysis for biopharmaceutical development and biomarker discovery for clinical disease diagnosis.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据