Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:15938636rdf:typepubmed:Citationlld:pubmed
pubmed-article:15938636lifeskim:mentionsumls-concept:C0378502lld:lifeskim
pubmed-article:15938636lifeskim:mentionsumls-concept:C0392747lld:lifeskim
pubmed-article:15938636pubmed:issue23lld:pubmed
pubmed-article:15938636pubmed:dateCreated2005-6-7lld:pubmed
pubmed-article:15938636pubmed:abstractTextIron regulatory proteins (IRPs) regulate iron metabolism in mammalian cells. We used biophysical techniques to examine the solution properties of apo-IRP1 and apo-IRP2 and the interaction with their RNA ligand, the iron regulatory element (IRE). Sedimentation velocity and equilibrium experiments have shown that apo-IRP1 exists as an equilibrium mixture of monomers and dimers in solution, with an equilibrium dissociation constant in the low micromolar range and slow kinetic exchange between the two forms. However, only monomeric IRP1 is observed in complex with IRE. In contrast, IRP2 exists as monomer in both the apo-IRP2 form and in the IRP2/IRE complex. For both IRPs, sedimentation velocity and dynamic light-scattering experiments show a decrease of the Stokes radius upon binding of IRE. This conformational change was also observed by circular dichroism. Studies with an RNA molecule complementary to IRE indicate that, although specific base interactions can increase the stability of the protein/RNA complex, they are not essential for inducing this conformational change. The dynamic change of the IRP between different oligomeric and conformational states induced by interaction with IRE may play a role in the iron regulatory functions of IRPs.lld:pubmed
pubmed-article:15938636pubmed:languageenglld:pubmed
pubmed-article:15938636pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:15938636pubmed:citationSubsetIMlld:pubmed
pubmed-article:15938636pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:15938636pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:15938636pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:15938636pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:15938636pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:15938636pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:15938636pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:15938636pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:15938636pubmed:statusMEDLINElld:pubmed
pubmed-article:15938636pubmed:monthJunlld:pubmed
pubmed-article:15938636pubmed:issn0006-2960lld:pubmed
pubmed-article:15938636pubmed:authorpubmed-author:SchuckPeterPlld:pubmed
pubmed-article:15938636pubmed:authorpubmed-author:YikilmazEmine...lld:pubmed
pubmed-article:15938636pubmed:authorpubmed-author:RouaultTracey...lld:pubmed
pubmed-article:15938636pubmed:issnTypePrintlld:pubmed
pubmed-article:15938636pubmed:day14lld:pubmed
pubmed-article:15938636pubmed:volume44lld:pubmed
pubmed-article:15938636pubmed:ownerNLMlld:pubmed
pubmed-article:15938636pubmed:authorsCompleteYlld:pubmed
pubmed-article:15938636pubmed:pagination8470-8lld:pubmed
pubmed-article:15938636pubmed:dateRevised2006-11-15lld:pubmed
pubmed-article:15938636pubmed:meshHeadingpubmed-meshheading:15938636...lld:pubmed
pubmed-article:15938636pubmed:meshHeadingpubmed-meshheading:15938636...lld:pubmed
pubmed-article:15938636pubmed:meshHeadingpubmed-meshheading:15938636...lld:pubmed
pubmed-article:15938636pubmed:meshHeadingpubmed-meshheading:15938636...lld:pubmed
pubmed-article:15938636pubmed:meshHeadingpubmed-meshheading:15938636...lld:pubmed
pubmed-article:15938636pubmed:meshHeadingpubmed-meshheading:15938636...lld:pubmed
pubmed-article:15938636pubmed:meshHeadingpubmed-meshheading:15938636...lld:pubmed
pubmed-article:15938636pubmed:meshHeadingpubmed-meshheading:15938636...lld:pubmed
pubmed-article:15938636pubmed:meshHeadingpubmed-meshheading:15938636...lld:pubmed
pubmed-article:15938636pubmed:meshHeadingpubmed-meshheading:15938636...lld:pubmed
pubmed-article:15938636pubmed:meshHeadingpubmed-meshheading:15938636...lld:pubmed
pubmed-article:15938636pubmed:meshHeadingpubmed-meshheading:15938636...lld:pubmed
pubmed-article:15938636pubmed:meshHeadingpubmed-meshheading:15938636...lld:pubmed
pubmed-article:15938636pubmed:meshHeadingpubmed-meshheading:15938636...lld:pubmed
pubmed-article:15938636pubmed:meshHeadingpubmed-meshheading:15938636...lld:pubmed
pubmed-article:15938636pubmed:meshHeadingpubmed-meshheading:15938636...lld:pubmed
pubmed-article:15938636pubmed:meshHeadingpubmed-meshheading:15938636...lld:pubmed
pubmed-article:15938636pubmed:meshHeadingpubmed-meshheading:15938636...lld:pubmed
pubmed-article:15938636pubmed:year2005lld:pubmed
pubmed-article:15938636pubmed:articleTitleSelf-association and ligand-induced conformational changes of iron regulatory proteins 1 and 2.lld:pubmed
pubmed-article:15938636pubmed:affiliationCell Biology and Metabolism Branch, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892-5766, USA.lld:pubmed
pubmed-article:15938636pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:15938636pubmed:publicationTypeComparative Studylld:pubmed
entrez-gene:48entrezgene:pubmedpubmed-article:15938636lld:entrezgene
entrez-gene:3658entrezgene:pubmedpubmed-article:15938636lld:entrezgene
http://linkedlifedata.com/r...entrezgene:pubmedpubmed-article:15938636lld:entrezgene
http://linkedlifedata.com/r...entrezgene:pubmedpubmed-article:15938636lld:entrezgene
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:15938636lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:15938636lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:15938636lld:pubmed