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Functionalization of decavanadate anion by coordination to cobalt(II): Binding to proteins, cytotoxicity, and water oxidation catalysis

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F23%3A10465377" target="_blank" >RIV/00216208:11310/23:10465377 - isvavai.cz</a>

  • Result on the web

    <a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=_JeterFiBi" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=_JeterFiBi</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.jinorgbio.2022.112067" target="_blank" >10.1016/j.jinorgbio.2022.112067</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Functionalization of decavanadate anion by coordination to cobalt(II): Binding to proteins, cytotoxicity, and water oxidation catalysis

  • Original language description

    A series of five decavanadates (V(10)) using a simple, one-pot synthesis, adhering to the model template: transition metal ion - decavanadate - ligands:(Hnicotinamide)(2){[Co(H2O)(3)(nicotinamide)(2)](2)[μ-V10O28]} . 6H2O (1), {[Co(H2O)(4)(isonicotinamide)(2)](3)}V10O28 . 4H2O (2), {[Co(H2O)(4)](2)[Co(H2O)2(μ-pyrazinamide)2][μ-V10O28]} . 4H2O (3) {[Co(H2O)(4)(μ-pyrazinamide)](3).V10O28} . 4H2O (4), and (NH4)(2){[Ni(H2O)(4)(2-hydroxyethylpyridine)](2)}V10O28 . 2H2O (5) was synthesized. X-ray analysis reveals that 1 and 3 are decavanadato complexes, while 2, 4 and 5 are decavanadate complex salts. Moreover, 3 is the first example of a polymeric decavanadato complex, employing direct coordination with the metal center and the organic ligand, in toto. From the solution studies using V-51 NMR spectroscopy, it was decoded that 1 and 3 stay stable in the model buffer solution and aqueous media. Binding to model proteins, cytotoxicity and water oxidation catalysis (WOC) was studied primarily for 1 and 3 and concluded that neither 1 nor 3 have an interaction with the model proteins thaumatin, lysozyme and pro-teinase K, because of the presence of the organic ligands in the Co(II) center, any further interplay with the proteins was blocked. Cytotoxicity studies reveal that 1 is 40% less toxic (0.05 mM) and 26% less toxic (0.1 mM) than the uncoordinated V(10) with human cell lines A549 and HeLa respectively. In WOC, 1 performed superior activity, by evolving 143.37 nmol of O2 which is 700% (9-fold) increase than the uncoordinated V(10).

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10402 - Inorganic and nuclear chemistry

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2023

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Journal of Inorganic Biochemistry

  • ISSN

    0162-0134

  • e-ISSN

    1873-3344

  • Volume of the periodical

    239

  • Issue of the periodical within the volume

    February

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    13

  • Pages from-to

    112067

  • UT code for WoS article

    000913192100003

  • EID of the result in the Scopus database

    2-s2.0-85142321312