Hossler Patrick, Goh Lin-Tang, Lee May May, Hu Wei-Shou
Department of Chemical Engineering and Materials Science, University of Minnesota, 421 Washington Avenue SE, Minneapolis, Minnesota 55455-0132, USA.
Biotechnol Bioeng. 2006 Dec 5;95(5):946-60. doi: 10.1002/bit.21062.
Glycosylation has profound effects on the quality of recombinant proteins produced in mammalian cells. The biosynthetic pathways of N-linked glycans on glycoproteins involves a relatively small number of enzymes and nucleotide sugars. Many of these glycoconjugate enzymes can utilize multiple N-glycans as substrates, thus generating a large number of glycan intermediates, and making the biosynthetic pathway resemble a network with diverging and converging paths. The N-glycans on secreted glycoprotein molecules include not only terminal glycans, but also pathway intermediates. To better assess the glycan distribution and the potential route of their synthesis, we created GlycoVis, a visualization program that displays the distribution and the potential reaction paths leading to each N-glycan on the reaction network. The substrate specificities of the enzymes involved were organized into a relationship matrix. With the input of glycan distribution data, the program outputs a reaction pathway map which labels the relative abundance levels of different glycans with different colors. The program also traces all possible reaction paths leading to each glycan and identifies each pathway on the map. Glycoform distribution of Chinese Hamster Ovary cell-derived tissue plasminogen activator (TPA), and human and mouse IgG were used as illustrations for the application of GlycoVis. In addition, the intracellular and secreted IgG from an NS0 producer cell line were isolated, and their glycoform profiles were displayed using GlycoVis for comparison. This visualization tool facilitates the analysis of potential reaction paths utilized under different physiological or culture conditions, and may provide insight on the potential targets for metabolic engineering.
糖基化对哺乳动物细胞中产生的重组蛋白质量有深远影响。糖蛋白上N-连接聚糖的生物合成途径涉及相对较少的酶和核苷酸糖。许多这些糖缀合物酶可以利用多种N-聚糖作为底物,从而产生大量聚糖中间体,使生物合成途径类似于具有发散和汇聚路径的网络。分泌型糖蛋白分子上的N-聚糖不仅包括末端聚糖,还包括途径中间体。为了更好地评估聚糖分布及其潜在的合成途径,我们创建了GlycoVis,这是一个可视化程序,可显示反应网络上每种N-聚糖的分布和潜在反应路径。将所涉及酶的底物特异性整理成一个关系矩阵。通过输入聚糖分布数据,该程序输出一个反应途径图,用不同颜色标记不同聚糖的相对丰度水平。该程序还追踪导致每种聚糖的所有可能反应路径,并在图上识别每条路径。以中国仓鼠卵巢细胞衍生的组织纤溶酶原激活剂(TPA)以及人和小鼠IgG的糖型分布为例说明GlycoVis的应用。此外,分离了NS0生产细胞系的细胞内和分泌型IgG,并使用GlycoVis展示它们的糖型谱以供比较。这种可视化工具有助于分析在不同生理或培养条件下利用的潜在反应路径,并可能为代谢工程的潜在靶点提供见解。