理工学部 教授

戸谷 希一郎

トタニ キイチロウ  (Kiichiro Totani)

基本情報

所属
成蹊大学 理工学部 理工学科 教授
学位
博士(工学)(慶應義塾大学)

J-GLOBAL ID
201401094820177323
researchmap会員ID
B000243010

外部リンク

委員歴

 4

論文

 92
  • Taiki Kuribara, Mitsuaki Hirose, Naoya Tajima, Kiichiro Totani
    Trends in Glycoscience and Glycotechnology 36(213) E94-E103 2024年9月25日  
  • Mitsuaki Hirose, Yuto Nakamachi, Hasumi Muto, Akito Taira, Shinji Tanaka, Taiki Kuribara, Kiichiro Totani
    Carbohydrate Research 2024年6月  
  • Ruchio Usui, Akira Koizumi, Kyohei Nitta, Taiki Kuribara, Kiichiro Totani
    The Journal of Organic Chemistry 2023年10月20日  
  • Shigesaburo Ogawa, Katsuya Iuchi, Taro Tsubomura, Kiichiro Totani, Setsuko Hara
    Journal of oleo science 71(10) 1531-1540 2022年9月30日  
    In molecular biology research, a vitamin E (VE) vehicle (VE dissolved in organic solvent) is often added to water media without a stabilizer. However, the detailed behavior of VE colloids in water media is unclear. In this study, we reveal that VE nanoemulsion readily forms in water-based media through the existing protocol. The colloid size was changed from 39 nm to the submicron scale by adjusting the initial concentration of the VE solution and adding a buffer. The radical scavenging effect of the dispersed nanosized VEs is comparable to that of the water-soluble antioxidant Trolox, providing excellent antioxidant performance in colloid form. The cytoprotection effect of the VE colloids under a lipid oxidation condition largely depends on the size of the nanodispersion. Smaller dispersed particles are more efficient radical scavengers than larger particles for a constant VE amount owing to sophisticated uptake behavior of cell. This unveiled fundamental knowledge pave the way for a preparative protocol of stabilizer-free VE vehicles, which are expected to become widely used in molecular biology research.
  • Taiki Kuribara, Kiichiro Totani
    Biology 11(2) 199-199 2022年1月27日  
    Glycoprotein folding plays a critical role in sorting glycoprotein secretion and degradation in the endoplasmic reticulum (ER). Furthermore, relationships between glycoprotein folding and several diseases, such as type 2 diabetes and various neurodegenerative disorders, are indicated. Patients’ cells with type 2 diabetes, and various neurodegenerative disorders induce ER stress, against which the cells utilize the unfolded protein response for protection. However, in some cases, chronic and/or massive ER stress causes critical damage to cells, leading to the onset of ER stress-related diseases, which are categorized into misfolding diseases. Accumulation of misfolded proteins may be a cause of ER stress, in this respect, perturbation of oligomannose-type glycan processing in the ER may occur. A great number of studies indicate the relationships between ER stress and misfolding diseases, while little evidence has been reported on the connection between oligomannose-type glycan processing and misfolding diseases. In this review, we summarize alteration of oligomannose-type glycan processing in several ER stress-related diseases, especially misfolding diseases and show the possibility of these alteration of oligomannose-type glycan processing as indicators of diseases.

MISC

 36
  • 栗原大輝, 児島大河, 柴山佳大, 武田陽一, 戸谷希一郎
    日本化学会春季年会講演予稿集(Web) 102nd 2022年  
  • 栗原大輝, 児島大河, 柴山佳大, 武田陽一, 戸谷希一郎
    日本化学会春季年会講演予稿集(Web) 101st 2021年  
  • 栗原大輝, 柴山佳大, 平野真, 足立優花, 武田陽一, 伊藤幸成, 戸谷希一郎
    日本化学会春季年会講演予稿集(CD-ROM) 100th 2020年  
  • 栗原大輝, 柴山佳大, 平野真, 足立優花, 武田陽一, 伊藤幸成, 戸谷希一郎
    日本糖質学会年会要旨集 38th 2019年  
  • 戸谷 希一郎
    Trends in Glycoscience and Glycotechnology 31(181) SJ59-SJ60 2019年  
    <p>糖タンパク質品質管理はタンパク質上の高マンノース糖鎖をシグナルとして制御される。著者らは糖鎖プローブを基軸とした解析を通して、本機構が糖鎖認識以外の副次的要因によって相補的に制御されていることを見出した。例えば関連するほとんどの糖鎖認識タンパク質が、基質糖タンパク質のアグリコン状態の違いを識別して、活性を調節していることを明らかにした。また細胞内を模した分子クラウディング環境下において、糖鎖プロセシング行程の上流が加速され下流が減速されることを見出した。さらに肥満や2型糖尿病、骨粗鬆症などの疾患が糖タンパク質品質管理の稼働状況に影響を与えることも明らかにした。</p>

書籍等出版物

 6

講演・口頭発表等

 127

担当経験のある科目(授業)

 14

共同研究・競争的資金等の研究課題

 9