Halbeek H
Complex Carbohydrate Research Center, University of Georgia, Athens, GA.
Methods Mol Biol. 1993;17:115-48. doi: 10.1385/0-89603-215-9:115.
The biochemical/biomedical research community, the pharmaceutical industry, and, indeed, molecular biologists generally are faced with the increasing need for characterization of carbohydrate structures of recombinant glycoproteins and natural analogs. Cultured mammalian cells (such as Chinese hamster ovary [CHO] cells) are used to produce glycoproteins for therapeutic and diagnostic use because of their ability to perform glycosylation. The presence of oligosaccharide moieties is often compulsory to define several biological activities of glycoproteins, including clearance rate, immunogenicity, and specific biological activity. Since a number of factors that influence glycosylation still elude our control (such as culture environment and age of the cells), the same gene expressed in the same type of cell may not always yield a product with exactly the same glycosylation pattern, presenting drug batch quality-control problems for the pharmaceutical industry. Nuclear magnetic resonance (NMR) spectroscopy provides a powerful nondestructive means to characterize glycoprotein carbohydrates structurally and is an indispensable part of the current methodology of glycosylation site mapping.
生物化学/生物医学研究界、制药行业,实际上,分子生物学家总体上面临着越来越大的需求,即对重组糖蛋白和天然类似物的碳水化合物结构进行表征。培养的哺乳动物细胞(如中国仓鼠卵巢[CHO]细胞)因其进行糖基化的能力而被用于生产用于治疗和诊断的糖蛋白。寡糖部分的存在通常是定义糖蛋白多种生物学活性所必需的,包括清除率、免疫原性和特定生物学活性。由于许多影响糖基化的因素仍无法控制(如培养环境和细胞年龄),在同一类型细胞中表达的相同基因可能并不总是产生具有完全相同糖基化模式的产物,这给制药行业带来了药物批次质量控制问题。核磁共振(NMR)光谱提供了一种强大的非破坏性方法来从结构上表征糖蛋白碳水化合物,并且是当前糖基化位点图谱绘制方法中不可或缺的一部分。