Počet záznamů: 1  

Optimizing the Inhibition of a Uniquely Composed Trypanosoma brucei F1-ATPase

  1. 1.
    SYSNO ASEP0488324
    Druh ASEPO - Ostatní výsledky
    Zařazení RIVO - Ostatní
    NázevOptimizing the Inhibition of a Uniquely Composed Trypanosoma brucei F1-ATPase
    Tvůrce(i) Gahura, Ondřej (BC-A) RID, ORCID
    Váchová, H. (CZ)
    Panicucci, Brian (BC-A)
    Walker, J.E. (GB)
    Zíková, Alena (BC-A) RID, ORCID
    Rok vydání2014
    Jazyk dok.eng - angličtina
    Země vyd.CZ - Česká republika
    Klíč. slovainhibition ; ATPase ; protein
    Vědní obor RIVEB - Genetika a molekulární biologie
    Obor OECDBiochemistry and molecular biology
    CEPLL1205 GA MŠMT - Ministerstvo školství, mládeže a tělovýchovy
    Institucionální podporaBC-A - RVO:60077344
    AnotaceThe transition of the parasitic Trypanosoma brucei between its invertebrate and vertebrate hosts is associated with substantial bioenergetic pathway changes. While substrate and oxidative phosphorylation (OXPHOS) provide the main source of ATP in the procyclic stage (PS), increased glycolysis of abundant glucose in the bloodstream form (BS) compensates for the absence of OXPHOS - requiring the F1Fo-ATPase to maintain the mitochondrial membrane potential at the expense of ATP. A widespread natural protein inhibitor of F1Fo-ATPase activity (TbIF1) is expressed in PS, while its ectopic expression is lethal in BS. To characterize TbIF1 inhibition, we isolated the F1-ATPase from PS by two-step chromatography. Besides the conserved eukaryotic components (3 3), the complex contains an additional trypanosomatid-specific protein, p18. The previously reported subunit cleavage was confirmed and modeled to a region presumed to form a loop between the crown and NTP-binding domains, a unique feature of F1-ATPase in Kinetoplastids. Furthermore, several recombinant TbIF1 mutants were characterized to determine their dissociation constants and oligomerization properties. While the C-terminal deletion of TbIF1 prevents homodimerization, it does not disrupt the pH sensitivity as it does in bovine IF1. Importantly, TbIF1 cannot inhibit bovine F1-ATPase and vice versa, strengthening the differences between the parasite and mammals. The established purification of a uniquely composed F1-ATPase is suitable for structure resolution by X-ray crystallography. Given the non-conventional function of F1-ATPase in BS and the F1-TbIF1 binding data, we propose that the structure could be exploited to design specific inhibitors for potential use in therapeutics.
    PracovištěBiologické centrum (od r. 2006)
    KontaktDana Hypšová, eje@eje.cz, Tel.: 387 775 214
    Rok sběru2018
    Elektronická adresahttp://www.parazitologie.cz/protozoologie/Protodny2014/JPD_sbornik_2014.pdf
Počet záznamů: 1  

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