BIROn - Birkbeck Institutional Research Online

    Dodecameric structure and ATPase activity of the human TIP48/TIP49 complex

    Puri, T. and Wendler, Petra and Sigala, B. and Saibil, Helen R. and Tsaneva, I.R. (2007) Dodecameric structure and ATPase activity of the human TIP48/TIP49 complex. Journal of Molecular Biology 366 (1), 179 - 192. ISSN 0022-2836.

    Full text not available from this repository.

    Abstract

    TIP48 and TIP49 are two related and highly conserved eukaryotic AAA+ proteins with an essential biological function and a critical role in major pathways that are closely linked to cancer. They are found together as components of several highly conserved chromatin-modifying complexes. Both proteins show sequence homology to bacterial RuvB but the nature and mechanism of their biochemical role remain unknown. Recombinant human TIP48 and TIP49 were assembled into a stable high molecular mass equimolar complex and tested for activity in vitro. TIP48/TIP49 complex formation resulted in synergistic increase in ATPase activity but ATP hydrolysis was not stimulated in the presence of single-stranded, double-stranded or four-way junction DNA and no DNA helicase or branch migration activity could be detected. Complexes with catalytic defects in either TIP48 or TIP49 had no ATPase activity showing that both proteins within the TIP48/TIP49 complex are required for ATP hydrolysis. The structure of the TIP48/TIP49 complex was examined by negative stain electron microscopy. Three-dimensional reconstruction at 20 Å resolution revealed that the TIP48/TIP49 complex consisted of two stacked hexameric rings with C6 symmetry. The top and bottom rings showed substantial structural differences. Interestingly, TIP48 formed oligomers in the presence of adenine nucleotides, whilst TIP49 did not. The results point to biochemical differences between TIP48 and TIP49, which may explain the structural differences between the two hexameric rings and could be significant for specialised functions that the proteins perform individually.

    Metadata

    Item Type: Article
    Keyword(s) / Subject(s): TIP48 (RUVBL2), TIP49 (RUVBL1), AAA+ protein, dodecamer, ATPase
    School: Birkbeck Faculties and Schools > Faculty of Science > School of Natural Sciences
    Research Centres and Institutes: Structural Molecular Biology, Institute of (ISMB)
    Depositing User: Administrator
    Date Deposited: 04 Aug 2011 12:33
    Last Modified: 02 Aug 2023 16:55
    URI: https://eprints.bbk.ac.uk/id/eprint/3989

    Statistics

    Activity Overview
    6 month trend
    0Downloads
    6 month trend
    221Hits

    Additional statistics are available via IRStats2.

    Archive Staff Only (login required)

    Edit/View Item Edit/View Item