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Cysteamine assay for the evaluation of bioactive electrophiles

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    0542079 - BFÚ 2022 RIV US eng J - Journal Article
    Novák, D. - Vrba, J. - Zatloukalová, M. - Roubalová, L. - Stolarczyk, K. - Dorčák, Vlastimil - Vacek, J.
    Cysteamine assay for the evaluation of bioactive electrophiles.
    Free Radical Biology and Medicine. Roč. 164, FEB 20 2021 (2021), s. 381-389. ISSN 0891-5849. E-ISSN 1873-4596
    R&D Projects: GA ČR(CZ) GA19-09212S
    Institutional support: RVO:68081707
    Keywords : Thiol reactivity * Cysteamine assay * Electrochemistry * Hydrophilic interaction chromatography * Nrf2 pathway
    OECD category: Biochemistry and molecular biology
    Impact factor: 8.101, year: 2021
    Method of publishing: Limited access
    https://www.sciencedirect.com/science/article/pii/S0891584921000137?via%3Dihub

    Covalent modifications of thiol and amine groups may control the function of proteins involved in the regulatory and signaling pathways of the cell. In this study, we developed a simple cysteamine assay which can be used to study the reactivity of electrophilic compounds towards primary amine and thiol groups in an aqueous environment. The detection principle is based on the electrochemical, photometrical and mass spectrometric analyses of cysteamine (2-aminoethanethiol) as the molecular probe. This technique is useful for studying the reaction kinetics of electrophiles with thiol (SH) and amino (NH2) groups. The decrease in analytical responses of cysteamine was monitored to evaluate the reactivity of three electrophilic activators of the Nrf2 pathway, which mediates the cellular stress response. The SH-reactivity under cell-free conditions of the tested electrophiles decreased in the following order: 4-hydroxy-2-nonenal >= nitro-oleic acid > sulforaphane. However, as shown in RAW264.7 cells, the tested compounds activated Nrf2-dependent gene expression in the opposite order: sulforaphane > nitro-oleic acid >= 4-hydroxy-2-nonenal. Although other factors in addition to chemical reactivity play a role in biological systems, we conclude that this cysteamine assay is a useful tool for screening potentially bioactive electrophiles and for studying their reactivity at a molecular level.
    Permanent Link: http://hdl.handle.net/11104/0319569

     
     
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