Optimization of a Myc-Interfering Peptide Based on Molecular Dynamics Simulations
Dateien
Datum
Autor:innen
Herausgeber:innen
ISSN der Zeitschrift
Electronic ISSN
ISBN
Bibliografische Daten
Verlag
Schriftenreihe
Auflagebezeichnung
URI (zitierfähiger Link)
DOI (zitierfähiger Link)
Internationale Patentnummer
Angaben zur Forschungsförderung
Projekt
Open Access-Veröffentlichung
Sammlungen
Core Facility der Universität Konstanz
Titel in einer weiteren Sprache
Publikationstyp
Publikationsstatus
Erschienen in
Zusammenfassung
Previously, a Myc-interfering peptide (Mip) was identified for the targeted inactivation of the Myc:Max complex by the combination of rational design and an in vivo protein-fragment complementation assay. In the subsequent work presented here, molecular dynamics simulations and free energy calculations based on the molecular mechanics GBSA method were performed to define the contribution of the different amino acids in the Myc:Mip coiled coil domain, and compared to wild-type Myc:Max. For further optimization of the Myc interference, point mutations were introduced into Mip and analyzed, from which two showed much higher binding affinities in the computational studies in good agreement with the experiment. These mutants with very high potential for inactivation of Myc can now be used as starting point for further optimizations based on the computational as well as experimental protocols presented here.
Zusammenfassung in einer weiteren Sprache
Fachgebiet (DDC)
Schlagwörter
Konferenz
Rezension
Zitieren
ISO 690
JOUAUX, Eva M, Barbara TIMM, Katja M. ARNDT, Thomas E. EXNER, 2009. Optimization of a Myc-Interfering Peptide Based on Molecular Dynamics Simulations. In: Journal of Peptide Science. 2009, 15(1), pp. 5-15. ISSN 1075-2617. eISSN 1099-1387. Available under: doi: 10.1002/psc.1078BibTex
@article{Jouaux2009Optim-1065, year={2009}, doi={10.1002/psc.1078}, title={Optimization of a Myc-Interfering Peptide Based on Molecular Dynamics Simulations}, number={1}, volume={15}, issn={1075-2617}, journal={Journal of Peptide Science}, pages={5--15}, author={Jouaux, Eva M and Timm, Barbara and Arndt, Katja M. and Exner, Thomas E.} }
RDF
<rdf:RDF xmlns:dcterms="http://purl.org/dc/terms/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:bibo="http://purl.org/ontology/bibo/" xmlns:dspace="http://digital-repositories.org/ontologies/dspace/0.1.0#" xmlns:foaf="http://xmlns.com/foaf/0.1/" xmlns:void="http://rdfs.org/ns/void#" xmlns:xsd="http://www.w3.org/2001/XMLSchema#" > <rdf:Description rdf:about="https://kops.uni-konstanz.de/server/rdf/resource/123456789/1065"> <dcterms:isPartOf rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/29"/> <dc:contributor>Exner, Thomas E.</dc:contributor> <dcterms:bibliographicCitation>Publ. in: Journal of Peptide Science 15 (2009), pp. 5-15</dcterms:bibliographicCitation> <foaf:homepage rdf:resource="http://localhost:8080/"/> <dspace:isPartOfCollection rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/52"/> <void:sparqlEndpoint rdf:resource="http://localhost/fuseki/dspace/sparql"/> <dc:creator>Timm, Barbara</dc:creator> <dcterms:abstract>Previously, a Myc-interfering peptide (Mip) was identified for the targeted inactivation of the Myc:Max complex by the combination of rational design and an in vivo protein-fragment complementation assay. In the subsequent work presented here, molecular dynamics simulations and free energy calculations based on the molecular mechanics GBSA method were performed to define the contribution of the different amino acids in the Myc:Mip coiled coil domain, and compared to wild-type Myc:Max. For further optimization of the Myc interference, point mutations were introduced into Mip and analyzed, from which two showed much higher binding affinities in the computational studies in good agreement with the experiment. These mutants with very high potential for inactivation of Myc can now be used as starting point for further optimizations based on the computational as well as experimental protocols presented here.</dcterms:abstract> <dc:creator>Jouaux, Eva M</dc:creator> <dspace:isPartOfCollection rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/29"/> <dc:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2011-03-22T17:55:03Z</dc:date> <dc:contributor>Timm, Barbara</dc:contributor> <dcterms:issued>2009</dcterms:issued> <dc:language>deu</dc:language> <dc:creator>Exner, Thomas E.</dc:creator> <dcterms:isPartOf rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/52"/> <dcterms:available rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2011-03-22T17:55:03Z</dcterms:available> <dcterms:title>Optimization of a Myc-Interfering Peptide Based on Molecular Dynamics Simulations</dcterms:title> <dc:contributor>Arndt, Katja M.</dc:contributor> <dcterms:rights rdf:resource="https://rightsstatements.org/page/InC/1.0/"/> <bibo:uri rdf:resource="http://kops.uni-konstanz.de/handle/123456789/1065"/> <dc:contributor>Jouaux, Eva M</dc:contributor> <dc:creator>Arndt, Katja M.</dc:creator> <dc:rights>terms-of-use</dc:rights> </rdf:Description> </rdf:RDF>