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用于粘蛋白型 O-糖基化网络生成和可视化的集成平台。

An integrated platform for mucin-type O-glycosylation network generation and visualization.

机构信息

Department of Chemical Engineering and Materials Science, University of Minnesota, Minneapolis, Minnesota.

出版信息

Biotechnol Bioeng. 2019 Jun;116(6):1341-1354. doi: 10.1002/bit.26952. Epub 2019 Mar 1.

DOI:10.1002/bit.26952
PMID:30739313
Abstract

Mucin-type O-glycans have profound effects on the structure and stability of glycoproteins. O-Glycans on the cell surface proteins also modulate the cell's interactions with the surrounding environments and other cells. The synthetic pathway of O-glycans involves a large number of enzymes with diverse substrate specificity. The expression pattern of these enzymes is cell and tissue-specific, thus making the pathway highly diverse. To facilitate pathway analysis in a cell and tissue-specific fashion, we developed an integrated platform of RING (Rule Input Network Generator) and O-GlycoVis. RING uses an English-like reaction language to describe the substrate specificity of enzymes and additional constraints on the formation of the glycan products. Using this information, the RING generates a list of possible glycans, which is used as input into O-Glycovis. O-GlycoVis displays the glycan distribution in the pathway and potential reaction paths leading to each glycan. With the input glycan data, O-GlycoVis also traces all possible reaction paths leading to each glycan and outputs pathway maps with the relative abundance levels of glycans overlaid. O-Glycan profiles from two breast cancer cell lines, MCF7 and T47d, human umbilical vascular endothelium cells, Chinese Hamster Ovary cells were generated based on transcriptional data and compared with experimentally observed O-glycans. This RING-based program allows rules to be added or subtracted for network generation and visualization of networks of O-glycosylation network of different tissues and species.

摘要

黏蛋白型 O-聚糖对糖蛋白的结构和稳定性有深远影响。细胞表面蛋白上的 O-聚糖也调节细胞与周围环境和其他细胞的相互作用。O-聚糖的合成途径涉及具有多种底物特异性的大量酶。这些酶的表达模式具有细胞和组织特异性,因此使途径具有高度多样性。为了促进细胞和组织特异性途径分析,我们开发了 RING(规则输入网络生成器)和 O-GlycoVis 的集成平台。RING 使用类似于英语的反应语言来描述酶的底物特异性以及对聚糖产物形成的附加约束。使用此信息,RING 生成可能的聚糖列表,该列表用作 O-GlycoVis 的输入。O-GlycoVis 显示途径中的聚糖分布以及导致每种聚糖的潜在反应途径。使用输入的聚糖数据,O-GlycoVis 还追踪导致每种聚糖的所有可能反应途径,并输出具有叠加的聚糖相对丰度水平的途径图。根据转录数据生成了来自两种乳腺癌细胞系 MCF7 和 T47d、人脐血管内皮细胞、中国仓鼠卵巢细胞的 O-聚糖图谱,并与实验观察到的 O-聚糖进行了比较。基于 RING 的程序允许添加或减去规则,以生成不同组织和物种的 O-糖基化网络的网络生成和可视化。

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