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Discovery of a novel ligand that modulates the protein?protein interactions of the AAA+ superfamily oncoprotein reptin

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00209805%3A_____%2F15%3A%230000612" target="_blank" >RIV/00209805:_____/15:#0000612 - isvavai.cz</a>

  • Result on the web

    <a href="http://pubs.rsc.org/en/content/articlepdf/2015/sc/c4sc03885a" target="_blank" >http://pubs.rsc.org/en/content/articlepdf/2015/sc/c4sc03885a</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1039/c4sc03885a" target="_blank" >10.1039/c4sc03885a</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Discovery of a novel ligand that modulates the protein?protein interactions of the AAA+ superfamily oncoprotein reptin

  • Original language description

    Developing approaches to discover protein?protein interactions (PPIs) remains a fundamental challenge. A chemical biology platform is applied here to identify novel PPIs for the AAA+ superfamily oncoprotein reptin. An in silico screen coupled with chemical optimization provided Liddean, a nucleotide-mimetic which modulates reptin's oligomerization status, protein-binding activity and global conformation. Combinatorial peptide phage library screening of Liddean-bound reptin with next generation sequencing identified interaction motifs including a novel reptin docking site on the p53 tumor suppressor protein. Proximity ligation assays demonstrated that endogenous reptin forms a predominantly cytoplasmic complex with its paralog pontin in cancer cells andLiddean promotes a shift of this complex to the nucleus. An emerging view of PPIs in higher eukaryotes is that they occur through a striking diversity of linear peptide motifs. The discovery of a compound that alters reptin's protein int

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    EB - Genetics and molecular biology

  • OECD FORD branch

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2015

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Chemical science

  • ISSN

    2041-6539

  • e-ISSN

  • Volume of the periodical

    6

  • Issue of the periodical within the volume

    5

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    8

  • Pages from-to

    3109-3116

  • UT code for WoS article

    000353223100055

  • EID of the result in the Scopus database

    2-s2.0-84928152626