Papers - MIYAGAWA Atsushi

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  • Unique, Fast, and All-or-none Click Reaction on Cyclodextrin and Amylose Reviewed

    Hatsuo Yamamura,Kyohei Shimohara,Ryuji Kurata,Yusuke Fujita,Kensuke Murata,Takaaki Hayashi,Atsushi Miyagawa

    Chemistry Letters   42 ( 6 )   643 - 645   2013.06

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    Language:English   Publishing type:Research paper (scientific journal)  

  • Mimicking an antimicrobial peptide polymyxin B by use of cyclodextrin Reviewed

    Hatsuo Yamamura, Ken Suzuki, Kazuma Uchibori, Atsushi Miyagawa, Masao Kawai, Chie Ohmizo, Takashi Katsu

    Chemical Communications   48   892 - 894   2011.12

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    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1039/C1CC16369H

    Other Link: http://pubs.rsc.org/en/content/articlehtml/2012/cc/c1cc16369h

  • Promiscuous activity of ER glucosidase II discovered through donor specificity analysis of UGGT Reviewed

    Atsushi Miyagawa et al.

    Biochemical and Biophysical Research Communications   403 ( 3-4 )   322 - 328   2010.12

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    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)  

  • g-Cyclodextrins possessing an azido group and a triisopropylbenzenesulfonyl group as useful synthetic and authentic intermediates for unsymmetrically functionalized derivatives Reviewed

    Yoshihide Himeno, Atsushi Miyagawa, Masao Kawai, Hatsuo Yamamura

    Tetrahedron   65 ( 45 )   9474 - 9480   2009.11

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    Language:English   Publishing type:Research paper (scientific journal)  

  • gamma-Cyclodextrins possessing an azido group and a triisopropylbenzenesulfonyl group as useful synthetic and authentic intermediates for unsymmetrically functionalized derivatives Reviewed

    Yoshihide Himeno, Atsushi Miyagawa, Masao Kawai, Hatsuo Yamamura

    TETRAHEDRON   65 ( 45 )   9474 - 9480   2009.11

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    Language:English   Publishing type:Research paper (scientific journal)   Publisher:PERGAMON-ELSEVIER SCIENCE LTD  

    Seven isomers of cyclomaltooctaose (gamma-cyclodextrin) whose C6s were unsymmetrically disubstituted with both an azido group and an arenesulfonyloxy group were prepared and each of them was isolated by reversed phase chromatography. The assignment of the modified positions in each regioisomers was unambiguously performed by chemical correlation with the authentic compounds and chemical conversion to the 3,6-anhydro derivatives followed by high-resolution 2D-(1)H NMR (COSY, TOCSY, and HO-HAHA) analyses. The compounds are versatile synthetic and authentic intermediates to prepare sophisticated derivatives with two different functionalities at desired positions on the molecule for supramolecular chemistry. (C) 2009 Elsevier Ltd. All rights reserved.

    DOI: 10.1016/j.tet.2009.08.061

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  • Development of Membrane Filter with Oligosaccharide Immobilized by Click Chemistry for Influenza Virus Adsorption Reviewed

    Tomohisa Kato, Atsushi Miyagawa, Maria Carmelita Z. Kasuya, Kenichi Hatanaka

    The Open Chemical and Biomedical Methods Journal   2   13 - 17   2009.04

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    Language:English   Publishing type:Research paper (scientific journal)  

  • Elimination Filter for Verotoxins -Highly Adsorbing by Glycoconjugate Polymer- Reviewed

    A. Miyagawa, MC. Kasuya, K. Hatanaka

    Chemistry Letters   37 ( 4 )   438 - 439   2008.03

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    Language:English   Publishing type:Research paper (scientific journal)  

  • Purification by Centrifugal Partition Chromatography of amphiphilic compounds, glycolipids and pseudo-glycolipids synthesized by using cells Reviewed

    T. Kato, A. Miyagawa, MC. Kasuya, A. Ito, K. Hatanaka

    Journal of Chromatography A   1178 ( 1-2 )   154 - 159   2008.01

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    Language:English   Publishing type:Research paper (scientific journal)  

  • Alternative methods of globotrioside production using Vero cells a microcarrier system procedure Reviewed

    A. Miyagawa, MC. Kasuya, K. Hatanaka

    Chemistry Central Journal   1   26   2007.11

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    Language:English   Publishing type:Research paper (scientific journal)  

  • Alternative methods of globotrioside production using Vero cells: a microcarrier system procedure Reviewed

    Atsushi Miyagawa, Maria Carmelita Z. Kasuya, Kenichi Hatanaka

    CHEMISTRY CENTRAL JOURNAL   1   26   2007.11

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    Language:English   Publishing type:Research paper (scientific journal)   Publisher:BIOMED CENTRAL LTD  

    Background: Glycolipids are one component of cell membranes, and are found most prevalently at the surface of the plasma membrane. Animal cells take in amphipathic glycosides, which are later glycosylated after assimilation in biosynthetic pathways. Gycosylated glycosides are released outside of cells to the surrounding culture medium. This represents an accessible method of obtaining complex glycosides.
    Results: Vero cells are sensitive to Shiga toxins and are known to express the glycosides globotriaosyl ceramide (Gb3) and globotetraosyl ceramide (Gb4) on the surface of the plasma membrane. By administering amphipathic lactosides to Vero cells, the above mentioned glycolipids could be produced by the action of cellular enzymes. In our study, the optimum conditions (seeded cell number, incubated time period, 12-azidododecyl lactoside concentration and medium volume) for the production of Gb3 analogue were investigated. The 87.9 mu g/100 mm dish (11.7% yield) Gb3 analogue was produced under appropriate conditions. The large-scale culture of Vero cells using a microcarrier culture method with repetitions produced about 30 mg of the Gb3 analogue.
    Conclusion: The mass production of glycosides in Vero cells was carried out on a microcarrier with repeated administration of 12-azidododecyl lactoside. The results indicated that the use of both a microcarrier culture and repetition were highly effective in the production of Gb3, Gb4 and sialyl lactoside (GM3) type-oligosaccharides.

    DOI: 10.1186/1752-153X-1-26

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  • Inhibitory effects of glycopolymers having globotriose and/or lactose on cytotoxicity of Shiga toxin 1 Reviewed

    A. Miyagawa, MC. Kasuya, K. Hatanaka

    Carbohydrate Polymers   67 ( 2 )   260 - 264   2007.01

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    Language:English   Publishing type:Research paper (scientific journal)  

  • Applications of Immobilized Glycopolymers -Development and potentiality of the adsorption filter for influenza virus Reviewed

    A. Miyagawa, M. Nakane, K. Hatanaka

    seisan kenkyu   59 ( 2 )   110 - 113   2007.01

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    Language:English   Publishing type:Research paper (scientific journal)  

  • 糖鎖高分子の医療用途を考える

    宮川 淳、畑中 研一

    未来材料   6 ( 7 )   32 - 37   2006.07

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    Language:Japanese   Publishing type:Research paper (other academic)  

  • Structural Analysis of the Interaction between Shiga Toxin B Subunits and Linear Polymers Bearing Clustered Globotriose Residues Reviewed

    M. Watanabe, K. Igai, K. Matsuoka, A. Miyagawa, T. Watanabe, R. Yanoshita, Y. Samejima, D. Terunuma, Y. Natori, K. Nishikawa

    Infection and Immunity   74 ( 3 )   1984 - 1988   2006.03

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    Language:English   Publishing type:Research paper (scientific journal)  

  • Immobilization of Glycoconjugate Polymers on Cellulose Membrane for Affinity Separation Reviewed

    A. Miyagawa, MC. Kasuya, K. Hatanaka

    Bulletin of the Chemical Society of Japan   79 ( 2 )   348 - 356   2006.02

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    Language:English   Publishing type:Research paper (scientific journal)  

  • Development of dialyzer with immobilized glycoconjugate polymers for removal of Shiga-toxin Reviewed

    A. Miyagawa, M. Watanabe, K. Igai, MC. Kasuya, Y. Natori, K. Nishikawa, K. Hatanaka

    Biomaterials   27 ( 17 )   3304 - 3311   2006.02

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    Language:English   Publishing type:Research paper (scientific journal)  

  • Synthesis of polyesters from 5-hydroxymethyl-2-furfural as a starting material Reviewed

    K. Hatanaka, D. Yoshida, K. Okuyama, A. Miyagawa, K. Tamura, N. Sato, K. Hashimoto, M. Sagehashi, A. Sakoda

    Kobunshi Ronbunshu   62   316 - 320   2005.07

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    Language:English   Publishing type:Research paper (scientific journal)  

  • Syntheses of polyesters from 5-hydroxymethyl-2-furfural as a starting material Reviewed

    K Hatanaka, D Yoshida, K Okuyama, A Miyagawa, K Tamura, N Sato, K Hashimoto, M Sagehashi, A Sakoda

    KOBUNSHI RONBUNSHU   62 ( 7 )   316 - 320   2005

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    Language:Japanese   Publishing type:Research paper (scientific journal)   Publisher:SOC POLYMER SCIENCE JAPAN  

    Polyesters were synthesized from 5-hydroxymethyl-2-furfural (HMF), which can be prepared by pyrolysis of biomass or cellulose. 2,5-Bis (hydroxymethyl) furan (BHF), which was prepared by the reduction of HMF, and natural dicarboxylic acids such as succinic acid, fumaric acid, or maleic acid were polymerized to give polyesters. Polycondensations were carried out by two methods: one used acid chloride and the other one used a condensing reagent. Polycondensation of BHF and succinic acid gave a polymer of which the number averaged degree of polymerization was 30. NMR and IR spectra indicated that the obtained polymers have linear and regular polyesters. Copolymerization performed using the mixture of two kinds of dicarboxylic acids gave the copolymers. DSC measurements of polyesters showed the melting temperature and the grass transition temperature.

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  • Fluorous-tagged compound: a viable scaffold to prime oligosaccharide synthesis by cellular enzymes Reviewed

    MC. Kasuya, R. Cusi, O. Ishihara, A. Miyagawa, K. Hashimoto, T. Sato, K. Hatanaka

    Biochemical and Biophysical Research Communication   316 ( 3 )   599 - 604   2004.04

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    Language:English   Publishing type:Research paper (scientific journal)  

  • Synthesis of glycoconjugate polymer carrying globotriaose as artificial multivalent ligand for Shigatoxin-producing Escherichia coli O157: H7. Reviewed

    A. Miyagawa, H. Kurosawa, T. Watanabe, T. Koyama, D. Terunuma, K. Matsuoka

    Carbohydrate Polymers   57   441 - 450   2004.03

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    Language:English   Publishing type:Research paper (scientific journal)  

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