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Enzymatic synthesis of dimeric glycomimetic ligands of NK cell activation receptors

  1. 1.
    SYSNO ASEP0366522
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleEnzymatic synthesis of dimeric glycomimetic ligands of NK cell activation receptors
    Author(s) Drozdová, Anna (MBU-M)
    Bojarová, Pavla (MBU-M) ORCID
    Křenek, Karel (MBU-M)
    Weignerová, Lenka (MBU-M) RID
    Hensen, B. (DE)
    Elling, L. (DE)
    Christensen, H. (DK)
    Jensen, H.H. (DK)
    Pelantová, Helena (MBU-M) ORCID, RID
    Kuzma, Marek (MBU-M) ORCID, RID
    Bezouška, Karel (MBU-M)
    Krupová, Monika (MBU-M)
    Adámek, David (MBU-M)
    Slámová, Kristýna (MBU-M) RID, ORCID
    Křen, Vladimír (MBU-M) RID, ORCID
    Source TitleCarbohydrate Research. - : Elsevier - ISSN 0008-6215
    Roč. 346, č. 12 (2011), s. 1599-1609
    Number of pages11 s.
    Languageeng - English
    CountryNL - Netherlands
    Keywordsbeta-N-Acetylhexosaminidase ; alactosyltransferase ; Enzymatic glycosylation
    Subject RIVCE - Biochemistry
    R&D ProjectsGP203/09/P024 GA ČR - Czech Science Foundation (CSF)
    GD305/09/H008 GA ČR - Czech Science Foundation (CSF)
    GA303/09/0477 GA ČR - Czech Science Foundation (CSF)
    CEZAV0Z50200510 - MBU-M (2005-2011)
    UT WOS000292852100029
    DOI10.1016/j.carres.2011.04.043
    AnnotationThis work reveals new structural relationships in the complex process of the interaction between activation receptors of natural killer cells (rat NKR-P1, human CD69) and novel bivalent carbohydrate glycomimetics. The length, glycosylation pattern and linker structure of receptor ligands were examined with respect to their ability to precipitate the receptor protein from solution, which simulates the in vivo process of receptor aggregation during NK cell activation. It was found that di-LacdiNAc triazole compounds show optimal performance, reaching up to 100 percent precipitation of the present protein receptors, and achieving high immunostimulatory activities without any tendency to trigger activation-induced apoptosis. In the synthesis of the compounds tested, two enzymatic approaches were applied
    WorkplaceInstitute of Microbiology
    ContactEliška Spurná, eliska.spurna@biomed.cas.cz, Tel.: 241 062 231
    Year of Publishing2012
Number of the records: 1  

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