阿尔法
聚糖
糖基化
唾液酸
糖蛋白
化学
N-连接糖基化
生物化学
计算生物学
生物
血红蛋白
作者
J. Lee,Dongsu Choi,Inseong Choi,Mi-Kyung Park,Eunyoung Choi,Yoon Jung Lee,Jeehye Park,Yoo Hee Yang,Gyong Sik Ha,Hong Chul Jin,Kwang Pyo Kim
摘要
EPO analogues are representative glycoprotein drugs composed of heterogeneous, multiple antennary N ‐glycans. NESP® and Aranesp® are hyperglycosylated EPO, marketed under the same international nonproprietary name as darbepoetin alfa. The multiple antennary N ‐glycans are a key factor that increases the half‐life of the drug in the body, which is closely related to efficacy. Thus, control of N ‐glycosylation is important in providing patients with consistent efficacy. This paper reports on the comprehensive characterization of N ‐glycosylation of darbepoetin alfa products. The results of N ‐glycan analysis of NESP® and Aranesp® showed difference in the ratio of N ‐glycans containing N ‐acetyllactosamine and O ‐acetylated sialic acid. Although there were some differences, the overall N ‐glycan structures and profiles were comparable. In particular, darbepoetin alfa products accounted for the largest proportion of tetra‐sialo N ‐glycans, greater than 75%. This study increases understanding of N ‐glycan profiles and structural information of darbepoetin alfa.
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