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Site-specific noncovalent interaction of the biopolymer poly(ADP-ribose) with the Werner syndrome protein regulates protein functions

Site-specific noncovalent interaction of the biopolymer poly(ADP-ribose) with the Werner syndrome protein regulates protein functions

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POPP, Oliver, Sebastian VEITH, Jörg FAHRER, Vilhelm BOHR, Alexander BÜRKLE, Aswin MANGERICH, 2013. Site-specific noncovalent interaction of the biopolymer poly(ADP-ribose) with the Werner syndrome protein regulates protein functions. In: ACS Chemical Biology. 8(1), pp. 179-188. ISSN 1554-8929. eISSN 1554-8937

@article{Popp2013-01-18Site--20750, title={Site-specific noncovalent interaction of the biopolymer poly(ADP-ribose) with the Werner syndrome protein regulates protein functions}, year={2013}, doi={10.1021/cb300363g}, number={1}, volume={8}, issn={1554-8929}, journal={ACS Chemical Biology}, pages={179--188}, author={Popp, Oliver and Veith, Sebastian and Fahrer, Jörg and Bohr, Vilhelm and Bürkle, Alexander and Mangerich, Aswin} }

<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:bibo="http://purl.org/ontology/bibo/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsd="http://www.w3.org/2001/XMLSchema#" > <rdf:Description rdf:about="https://kops.uni-konstanz.de/rdf/resource/123456789/20750"> <dcterms:title>Site-specific noncovalent interaction of the biopolymer poly(ADP-ribose) with the Werner syndrome protein regulates protein functions</dcterms:title> <dc:creator>Mangerich, Aswin</dc:creator> <dcterms:bibliographicCitation>ACS Chemical Biology ; 8 (2013), 1. - S. 179-188</dcterms:bibliographicCitation> <dc:creator>Popp, Oliver</dc:creator> <dc:contributor>Fahrer, Jörg</dc:contributor> <dc:creator>Veith, Sebastian</dc:creator> <dc:creator>Bohr, Vilhelm</dc:creator> <dc:contributor>Popp, Oliver</dc:contributor> <dcterms:available rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2013-01-21T08:12:48Z</dcterms:available> <dc:rights>deposit-license</dc:rights> <dc:creator>Fahrer, Jörg</dc:creator> <dc:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2013-01-21T08:12:48Z</dc:date> <dc:contributor>Bürkle, Alexander</dc:contributor> <bibo:uri rdf:resource="http://kops.uni-konstanz.de/handle/123456789/20750"/> <dc:language>eng</dc:language> <dcterms:issued>2013-01-18</dcterms:issued> <dc:contributor>Bohr, Vilhelm</dc:contributor> <dc:creator>Bürkle, Alexander</dc:creator> <dc:contributor>Veith, Sebastian</dc:contributor> <dc:contributor>Mangerich, Aswin</dc:contributor> <dcterms:rights rdf:resource="http://nbn-resolving.org/urn:nbn:de:bsz:352-20140905103605204-4002607-1"/> <dcterms:abstract>Werner syndrome is a premature aging disorder that is caused by defects in the Werner protein (WRN). WRN is a member of the RecQ helicase family and possesses helicase and exonuclease activities. It is involved in various aspects of DNA metabolism such as DNA repair, telomere maintenance, and replication. Poly(ADP-ribose) polymerase 1 (PARP1) is also involved in these processes by catalyzing the formation of the nucleic-acid-like biopolymer poly(ADP-ribose) (PAR). It was previously shown that WRN interacts with PARP1 and that WRN activity is inhibited by PARP1. Using several bioanalytical approaches, here we demonstrate that the enzymatic product of PARP1, i.e., PAR, directly interacts with WRN physically and functionally. First, WRN binds HPLC-size-fractionated short and long PAR in a noncovalent manner. Second, we identified and characterized a PAR-binding motif (PBM) within the WRN sequence and showed that several basic and hydrophobic amino acids are of critical importance for mediating the PAR binding. Third, PAR-binding inhibits the DNA-binding, the helicase and the exonuclease activities of WRN in a concentration-dependent manner. On the basis of our results we propose that the transient nature of PAR produced by living cells would provide a versatile and swiftly reacting control system for WRN's function. More generally, our work underscores the important role of noncovalent PAR-protein interactions as a regulatory mechanism of protein function.</dcterms:abstract> </rdf:Description> </rdf:RDF>

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