糖基化
重组DNA
聚糖
糖蛋白
受体
化学
T细胞受体
N-连接糖基化
细胞生物学
融合蛋白
生物
计算生物学
分子生物学
生物化学
T细胞
基因
免疫学
免疫系统
作者
Kai Zhang,Stephen J. Demarest,Xiufeng Wu,Jonathan R. Fitchett
标识
DOI:10.1007/978-1-4939-6857-2_12
摘要
Glycoprofiling recombinant proteins expressed and secreted from mammalian cells is key to understanding their interactions with glycoprotein receptors in vivo. Recently, recombinant T cell receptors (TCRs) are being considered as therapeutic moieties. Here we present a mass spectrometry based protocol with a "bottom up" approach to characterize glycosylation in recombinant fusion proteins with α/β TCR constant domains expressed in mammalian cells. The protocol focuses on using peptide mass mapping and mass spectrometry for N-linked glycan profiling, including analyses of site occupancy, glycan heterogeneity, and possible glycan compositions and structures.
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