RESEARCH

Glyco-Systems biology Division

Purpose / Contents

Deciphering glycan code from glycan big data

The purpose of the Systems Biology Division in the Integrated Glyco-Big Data Center (iGDATA) is to understand glycan functions and complexity by analyzing glycan-related big data using systems biology approaches. This will lead to the prediction of key biomarkers and drug targets. By collaborating with other divisions focusing on studies using model organisms and human samples, we will predict glycan structures associated with various diseases. To achieve this, we will develop algorithms, tools, and software targeting mass-spec-based glycomics and glycoproteomics data. In addition, we aim to develop a new interface that links genome science and glycoscience, which is an innovative platform for developing new strategies against various diseases.

Examples

Comprehensive understanding of changes in cellular glycans using mass-spectrometry

We have developed a new comprehensive method for the glycomic analysis of total cellular glycans using mass-spec, which enables us to detect glycan changes in various samples. Recently, we elucidated the changes in glycan structure in cells caused by the plant compound "swainsonine“, This compound is known to evoke toxic symptoms in domestic animals.
(Morikawa et al., BBA - General Subjects, 2022, 1866, 130168)

Members List

Yusuke Matsui

Division headSystems Biology Division

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Research interests
Statistical science, informatics, computational biology, computational neuroscience, bioinformatics
Research subject
Life science is generating huge and complex data at an unprecedented rate. Various and heterogeneous big data are being accumulated, including next-generation sequencing technology, mass spectrometry to capture proteome and post-translational modifications, and sensing technology to capture imaging and biological information. It is quite important to utilize such large-scale big data in life science in order to reveal the mechanisms of unknown biological systems. Our mission is to develop useful mathematical modeling and data analysis methods in life science.

Takaya Arita

Systems Biology Division

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Research interests
Artificial life, evolution dynamics, meta-recognition
Research subject
How can life's adaptive processes (evolution, development, learning) generate vitality? and how can language, cognition, and altruism, which constitute human social intelligence, evolve in this process? We conduct research on artificial life to pursue the logic to answer these two questions using a constructive method.

Motonori Ota

Systems Biology Division

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Research interests
Structure bioinformatics, protein tertiary structure, naturally denatured protein, protein-protein interaction network
Research subject
Our research focuses on bioinformatics related to protein conformations and how interactions and conformational changes lead to functions. We also develop algorithms (methods) for data analysis and constructing databases.

Kensaku Mori

Systems Biology Division

Hiroyuki Kaji

Systems Biology Division

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Research interests
Glycoproteomics, glycome, proteome, liquid chromatography, mass spectrometry
Research subject
We develop and apply techniques for comprehensive analysis of post-translational modifications of proteins, especially glycosylation, using mass spectrometry. We systematically analyze the structures of glycans attached to the glycosylation sites on each glycoprotein in biological samples such as body fluids, cells, and tissues, and when and how these glycans change. By obtaining this information, we hope to contribute to basic research such as elucidation of the involvement of glycans in biological phenomena as well as applied research on development of diagnostic markers and therapeutic targets presenting the altered glycans.

Jun-ichi Furukawa

Systems Biology Division

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Research interests
Glycomics, glycoprotein, glycosphingolipid, glycosaminoglycan, free oligosaccharide, SALSA method
Research subject
Cell surface is covered with various glycans whose levels and structures are known to change dramatically with cellular conditions and the environments. Various classes of glycans are present, including complex glycoconjugates such as glycoproteins and glycolipids, glycosaminoglycans such as heparan sulfate and chondroitin sulfate, and free oligosaccharides. We have developed a technique for comprehensive analysis of glycans and conduct total glycomics research on blood, cells, and tissues.

Morten Thaysen-Andersen

Systems Biology Division

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Research interests
Clinical glycoproteomics, Glycoimmunology, N-glycosylation, Cancer, Sepsis, Innate immunity
Research subject
The Glycoproteomics Lab@iGCORE develops and applies cutting-edge LC-MS/MS-based methods for quantitative and comparative glycoproteomics of human biospecimens to holistically explore elusive roles of protein N-glycosylation in human glycobiology with a particular focus on the innate immune system. The group uses high throughput glycoproteomics methods compatible with large clinical sample cohorts to study how the N-glycoproteome is remodelled with aberrant physiology and with various disorders including cancer, inflammation and infectious diseases.

Jennifer J. Kohler

Systems Biology Division

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Research interests
chemical biology, fucose, glycolipids, intestinal epithelia, mucus, infectious disease, genetic disorders of glycosylation
Research subject
The complex structures and properties of glycans are critical to their myriad biological functions. However, this complexity leads to technical challenges. To tackle these challenges, our research team has created chemical biology methods aimed at understanding glycan function. In particular, we developed photocrosslinking sugar analogs that can be metabolically incorporated into cellular glycoconjugates and used to covalently capture transient glycan-mediated interactions. Using one of these photocrosslinking sugars, we discovered that cholera toxin recognizes fucosylated glycoconjugates displayed on the surface of human intestinal epithelial cells. In current work, we are continuing to develop and apply chemical biology tools to problems in glycoscience. Additionally, we are probing the mechanisms that regulate production of glycoconjugates that comprise the mucosal layer of the intestinal epithelial. Our studies have relevance to infectious disease, cancer biology, and genetic disorders of glycosylation.

Rebeca Kawahara

Systems Biology Division

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Research interests
Clinical glycoproteomics, multi-omics, data integration, glycosignatures, diseases
Research subject
The focus of my research at the Glycoproteomics Lab@iGCORE consists in developing and applying advanced mass spectrometry-based glycoanalytical methods and multi-omics data integration systems in large cohorts of clinical samples to enable comprehensive and holistic profile of the human glycoproteome and the discovery of new glycosignatures associated with human diseases.

Ryuji Kato

Systems Biology Division

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Research interests
Image analysis, cell morphology, cell adhesion, cell quality control
Research subject
We aim to develop cell image analysis technique for cell quality control and develop culture scaffold materials for controlling cell quality. For this purpose, we label glycolipids in cell membranes and search for glycan binding peptides in cell membranes.

Nobuaki Miura

Systems Biology Division

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Research interests
Bioinformatics, glycomics, metaproteomics, computational chemistry, molecular structure theory, informatic coordination, DX promotion
Research subject
I am focusing on the field of mass spectrometry informatics in the hope of helping to elucidate new phenomena by extracting as much useful information as possible for life science from mass spectrometry spectral data. With the evolution of instruments, we encounter various evil spirits of mountains and rivers. I believe that it is our job as informaticians to analyze the data without prejudice, and to support the acquisition of new knowledge. At Nagoya University iGCORE, we are developing software such as Toolbox Accelerating Glycomics (TAG), a MALDI glycan analysis software suite, and Glyco Spectral Harvest (Harverst), which extracts glycan information from raw spectral data. We are conducting research to contribute to the spread and DX promotion of informatics through software development.

Hisatoshi Hanamatsu

Systems Biology Division

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Research interests
Glycan analysis, mass spectrometry, sialic acid
Research subject
To easily analyze various classes of complex glycoconjugate glycans in cells, tissues, and body fluids, we focus on the development of new subglycome analysis techniques, such as a chemical approach to identify sialic acid linkage patterns by mass spectrometry, a chemical cleavage method for O-type glycans without useful cleavage enzymes, and a new separation method for glycosaminoglycan disaccharides, to elucidate various glycan functions.

Shiori Go

Systems Biology Division

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Research interests
Glycolipid, glycoproteomics, intracellular trafficking
Research subject
We focus on the function of membrane microdomain in various biological phenomena on brain. In membrane microdomain, glycosphingolipids and specific glycoproteins are enriched, interact with each other, and regulate various biological functions. We are particularly interested in the elucidation of comprehensive functions of microdomains glycosylation in neural functions. We analyze structure of glycosphingolipids and glycans of glycoproteins in microdomain using methods for glycoproteomics and glycosphingolipids analysis.

Bingyuan ZHANG

Systems Biology Division

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Research interests
Statistical Science, Machine Learning, Bioinformatics
Research subject
Massive amounts of data from innovative technologies such as sequencing, mass spectrometry techniques present new challenges and exciting opportunities. My mission is to develop useful mathematical tools based on state-of-the-art statistical and machine learning techniques to utilize these large-scale heterogeneous real-world data to discover new mechanisms in unknown biological systems and ultimately contribute to scientific discovery.

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