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工具箱加速糖组学(TAG):基质辅助激光解吸电离飞行时间质谱 (MALDI-TOF MS) 谱的聚糖注释和将表达变化映射到生物合成途径。

Toolbox Accelerating Glycomics (TAG): Glycan Annotation from MALDI-TOF MS Spectra and Mapping Expression Variation to Biosynthetic Pathways.

机构信息

Division of Bioinformatics, Niigata University Graduate School of Medical and Dental Sciences, 1-757 Asahimachi-dori, Chuo-ku, Niigata 951-8510, Japan.

Department of Advanced Clinical Glycobiology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Kita21, Nishi11, Kita-ku, Sapporo 001-0021, Japan.

出版信息

Biomolecules. 2020 Sep 28;10(10):1383. doi: 10.3390/biom10101383.

Abstract

Glycans present extraordinary structural diversity commensurate with their involvement in numerous fundamental cellular processes including growth, differentiation, and morphogenesis. Unlike linear DNA and protein sequences, glycans have heterogeneous structures that differ in composition, branching, linkage, and anomericity. These differences pose a challenge to developing useful software for glycomic analysis. To overcome this problem, we developed the novel Toolbox Accelerating Glycomics (TAG) program. TAG consists of three units: 'TAG List' creates a glycan list that is used for database searching in TAG Expression; 'TAG Expression' automatically annotates and quantifies glycan signals and draws graphs; and 'TAG Pathway' maps the obtained expression information to biosynthetic pathways. Herein, we discuss the concepts, outline the TAG process, and demonstrate its potential using glycomic expression profile data from Chinese hamster ovary (CHO) cells and mutants lacking a functional gene ( knockout (KO) CHO cells). TAG not only drastically reduced the amount of time and labor needed for glycomic analysis but also detected and quantified more glycans than manual analysis. Although this study was limited to the analysis of -glycans and free oligosaccharides, the glycomic platform will be expanded to facilitate the analysis of -glycans and glycans of glycosphingolipids.

摘要

聚糖呈现出非凡的结构多样性,与它们在众多基本细胞过程中的参与是相称的,包括生长、分化和形态发生。与线性 DNA 和蛋白质序列不同,聚糖具有不同组成、分支、连接和异头物的异构结构。这些差异给开发用于糖组学分析的有用软件带来了挑战。为了克服这个问题,我们开发了新颖的糖组学加速工具箱 (TAG) 程序。TAG 由三个单元组成:“TAG List”创建一个聚糖列表,用于在 TAG Expression 中进行数据库搜索;“TAG Expression”自动注释和定量聚糖信号并绘制图形;“TAG Pathway”将获得的表达信息映射到生物合成途径上。在此,我们讨论了概念,概述了 TAG 过程,并使用来自中国仓鼠卵巢 (CHO) 细胞和缺乏功能 基因 (KO) CHO 细胞的突变体的糖组学表达谱数据演示了其潜力。TAG 不仅大大减少了糖组学分析所需的时间和劳动力,而且比手动分析检测和定量了更多的聚糖。尽管这项研究仅限于 -聚糖和游离寡糖的分析,但糖组学平台将扩展到 -聚糖和糖脂聚糖的分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1e0/7650810/0e4aecc1f7df/biomolecules-10-01383-g001.jpg

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