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The effect of mitochondrially targeted anticancer agents on mitochondrial (super)complexes

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    SYSNO ASEP0522123
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve SCOPUS
    TitleThe effect of mitochondrially targeted anticancer agents on mitochondrial (super)complexes
    Author(s) Vondrusová, Magdaléna (BTO-N) RID
    Bezawork-Geleta, A. (AU)
    Sachaphibulkij, K. (AU)
    Truksa, Jaroslav (BTO-N) RID, ORCID
    Neužil, Jiří (BTO-N) RID
    Number of authors5
    Source TitleMethods in molecular biology - ISSN 1940-6029
    Roč. 1265, č. 2015 (2015), s. 195-208
    Number of pages14 s.
    Languageeng - English
    CountryUS - United States
    Keywordsantineoplastic agent ; mitochondrial protein ; multienzyme complex
    Subject RIVEB - Genetics ; Molecular Biology
    OECD categoryBiochemistry and molecular biology
    Method of publishingLimited access
    Institutional supportBTO-N - RVO:86652036
    EID SCOPUS84958608088
    DOI10.1007/978-1-4939-2288-8_15
    AnnotationThe mitochondrial respiratory chain is organized into dynamic high molecular weight complexes that associate to form supercomplexes. The function of these SCs is to minimize the production of reactive oxygen species (ROS) generated during electron transfer within them and to efficiently transfer electrons to complex IV. These supra-molecular structures as well as whole mitochondria are stress-responsive and respond to mitochondrially targeted anti-cancer agent by destabilization and induction of massive production of ROS leading to apoptosis. We have recently developed mitochondrially targeted anti-cancer agents epitomized by the mitochondrially targeted analogue of the redox-silent compound vitamin E succinate, which belongs to the group of agents that kill cancer cells via their mitochondria-destabilizing activity, referred to as mitocans. To understand the molecular mechanism of the effect of such agents, the use of native blue gel electrophoresis and clear native electrophoresis coupled with in-gel activity assays, are methods of choice. The relevant methodology is described in this chapter.
    WorkplaceInstitute of Biotechnology
    ContactMonika Kopřivová, Monika.Koprivova@ibt.cas.cz, Tel.: 325 873 700
    Year of Publishing2020
    Electronic addresshttps://link.springer.com/protocol/10.1007%2F978-1-4939-2288-8_15
Number of the records: 1  

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