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Enzymatic preparation of glyconanomaterials

Public support

  • Provider

    Ministry of Education, Youth and Sports

  • Programme

    INTER-EXCELLENCE

  • Call for proposals

    SMSM2020LTC01

  • Main participants

    Mikrobiologický ústav AV ČR, v. v. i.

  • Contest type

    VS - Public tender

  • Contract ID

    MSMT-21080/2020-36

Alternative language

  • Project name in Czech

    Enzymatic preparation of glyconanomaterials

  • Annotation in Czech

    Major objective of this project proposal is to prepare rhamnose and rutinose containing glycoconjugates and multivalent structures with the use of advanced chemoenzymatic methods and bring these compounds into the applications in treatment of dermatological problems and diabetic ulcer complications. Rhamnosyl-rich oligo- and polysaccharides proved to be active in inhibiting most of the harmful effects of AGE-products - typically wrinkle formation and they demonstrated a potential to revert or diminish their negative consequences. This effect may be caused by the interaction with the hypothetic α-rhamnose-selective lectins e.g. in keratinocytes. We will prepare new multivalent rhamnose carrying structures based on the presentation of rutinosyl moieties (α-L-Rha(16)-β-D-Glc), which can be attached onto various spacers using enzymatic transglycosylation with recently discovered enzyme rutinosidase. These rhamnosyl neoglycoconjugates will be used for rhamnose lectin search and tested in biological assays for inhibitory activity towards AGE-mediated pathologies.

Scientific branches

  • R&D category

    ZV - Basic research

  • OECD FORD - main branch

    10608 - Biochemistry and molecular biology

  • OECD FORD - secondary branch

    30104 - Pharmacology and pharmacy

  • OECD FORD - another secondary branch

    30401 - Health-related biotechnology

  • CEP - equivalent branches <br>(according to the <a href="http://www.vyzkum.cz/storage/att/E6EF7938F0E854BAE520AC119FB22E8D/Prevodnik_oboru_Frascati.pdf">converter</a>)

    CE - Biochemistry<br>EB - Genetics and molecular biology<br>EI - Biotechnology and bionics<br>FR - Pharmacology and apothecary chemistry

Completed project evaluation

  • Provider evaluation

    V - Vynikající výsledky projektu (s mezinárodním významem atd.)

  • Project results evaluation

    The dual substrate specificity of Aspergillus niger rutinosidase and its substrate tunnel were discovered. This rutinosidase is capable of glycosylating inorganic azide. The native enzyme formed the beta-anomer and the mutant formed the alpha-anomer. Rutinose-based rhamnose derivatives interact with rhamnose recognising lectins and inhibit aging-related effects in the skin (anti-aging activity).

Solution timeline

  • Realization period - beginning

    Jun 1, 2020

  • Realization period - end

    Oct 3, 2023

  • Project status

    U - Finished project

  • Latest support payment

    Feb 17, 2023

Data delivery to CEP

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

  • Data delivery code

    CEP24-MSM-LT-U

  • Data delivery date

    Jul 1, 2024

Finance

  • Total approved costs

    3,858 thou. CZK

  • Public financial support

    3,858 thou. CZK

  • Other public sources

    0 thou. CZK

  • Non public and foreign sources

    0 thou. CZK