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A MALDI-MS-based quantitative glycoprofiling method on a 96-well plate platform

Authors
Kim, Kyoung-JinKim, Yoon-WooPark, Han-GyuHwang, Cheol-HwanPark, In YoungChoi, Kwon-YoungYang, Yung-HunKim, Young HwanKim, Yun-Gon
Issue Date
Feb-2017
Publisher
ELSEVIER SCIENCE INC
Keywords
High-throughput analysis; MALDI-MS; N-glycan; UPLC-FLR; Biopharmaceuticals
Citation
JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY, v.46, pp.150 - 156
Journal Title
JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY
Volume
46
Start Page
150
End Page
156
URI
http://scholarworks.bwise.kr/ssu/handle/2018.sw.ssu/6451
DOI
10.1016/j.jiec.2016.10.025
ISSN
1226-086X
Abstract
Here, we developed a high-throughput MALDI-MS based quantitative targeted glycomics (HT MALDI-QTaG) method for analyzing total N-glycans. Although the chemical derivatization processes (i.e., neutralization of sialic acid and incorporation of a positively-charged moiety) were performed in a 96-well with built-in 10 kDa MWCO membrane filters, the quantitative linearity was still quite good (R-2 > 0.99) between varying amounts of the target glycoprotein and the MALDI peak intensities. In addition, we validated the relative quantitative reproducibilities in different well positions in a 96-well plate. As a proof-of-concept, the proposed HT MALDI-QTaG method was successfully used to analyze bovine fetuin, human serum and Enbrel (R). (C) 2016 Published by Elsevier B.V. on behalf of The Korean Society of Industrial and Engineering Chemistry.
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