Laser-Induced Magnetic Dipole Spectroscopy

dc.contributor.authorHintze, Christian
dc.contributor.authorBücker, Dennis
dc.contributor.authorDomingo Köhler, Silvia
dc.contributor.authorJeschke, Gunnar
dc.contributor.authorDrescher, Malte
dc.date.accessioned2016-09-09T13:04:03Z
dc.date.available2016-09-09T13:04:03Z
dc.date.issued2016-06-16eng
dc.description.abstractPulse electron paramagnetic resonance measurements of nanometer scale distance distributions have proven highly effective in structural studies. They exploit the magnetic dipole-dipole coupling between spin labels site-specifically attached to macromolecules. The most commonly applied technique is double electron-electron resonance (DEER, also called pulsed electron double resonance (PELDOR)). Here we present the new technique of laser-induced magnetic dipole (LaserIMD) spectroscopy based on optical switching of the dipole-dipole coupling. In a proof of concept experiment on a model peptide, we find, already at a low quantum yield of triplet excitation, the same sensitivity for measuring the distance between a porphyrin and a nitroxide label as in a DEER measurement between two nitroxide labels. On the heme protein cytochrome C, we demonstrate that LaserIMD allows for distance measurements between a heme prosthetic group and a nitroxide label, although the heme triplet state is not directly observable by an electron spin echo.eng
dc.description.versionpublishedeng
dc.identifier.doi10.1021/acs.jpclett.6b00765eng
dc.identifier.pmid27163749eng
dc.identifier.urihttps://kops.uni-konstanz.de/handle/123456789/35203
dc.language.isoengeng
dc.subject.ddc540eng
dc.titleLaser-Induced Magnetic Dipole Spectroscopyeng
dc.typeJOURNAL_ARTICLEeng
dspace.entity.typePublication
kops.citation.bibtex
@article{Hintze2016-06-16Laser-35203,
  year={2016},
  doi={10.1021/acs.jpclett.6b00765},
  title={Laser-Induced Magnetic Dipole Spectroscopy},
  number={12},
  volume={7},
  journal={The Journal of Physical Chemistry Letters},
  pages={2204--2209},
  author={Hintze, Christian and Bücker, Dennis and Domingo Köhler, Silvia and Jeschke, Gunnar and Drescher, Malte}
}
kops.citation.iso690HINTZE, Christian, Dennis BÜCKER, Silvia DOMINGO KÖHLER, Gunnar JESCHKE, Malte DRESCHER, 2016. Laser-Induced Magnetic Dipole Spectroscopy. In: The Journal of Physical Chemistry Letters. 2016, 7(12), pp. 2204-2209. eISSN 1948-7185. Available under: doi: 10.1021/acs.jpclett.6b00765deu
kops.citation.iso690HINTZE, Christian, Dennis BÜCKER, Silvia DOMINGO KÖHLER, Gunnar JESCHKE, Malte DRESCHER, 2016. Laser-Induced Magnetic Dipole Spectroscopy. In: The Journal of Physical Chemistry Letters. 2016, 7(12), pp. 2204-2209. eISSN 1948-7185. Available under: doi: 10.1021/acs.jpclett.6b00765eng
kops.citation.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/123456789/35203">
    <bibo:uri rdf:resource="https://kops.uni-konstanz.de/handle/123456789/35203"/>
    <dc:contributor>Drescher, Malte</dc:contributor>
    <dc:contributor>Jeschke, Gunnar</dc:contributor>
    <dc:language>eng</dc:language>
    <void:sparqlEndpoint rdf:resource="http://localhost/fuseki/dspace/sparql"/>
    <dcterms:isPartOf rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/29"/>
    <dc:creator>Domingo Köhler, Silvia</dc:creator>
    <dc:contributor>Bücker, Dennis</dc:contributor>
    <dc:creator>Bücker, Dennis</dc:creator>
    <dc:contributor>Hintze, Christian</dc:contributor>
    <dcterms:abstract xml:lang="eng">Pulse electron paramagnetic resonance measurements of nanometer scale distance distributions have proven highly effective in structural studies. They exploit the magnetic dipole-dipole coupling between spin labels site-specifically attached to macromolecules. The most commonly applied technique is double electron-electron resonance (DEER, also called pulsed electron double resonance (PELDOR)). Here we present the new technique of laser-induced magnetic dipole (LaserIMD) spectroscopy based on optical switching of the dipole-dipole coupling. In a proof of concept experiment on a model peptide, we find, already at a low quantum yield of triplet excitation, the same sensitivity for measuring the distance between a porphyrin and a nitroxide label as in a DEER measurement between two nitroxide labels. On the heme protein cytochrome C, we demonstrate that LaserIMD allows for distance measurements between a heme prosthetic group and a nitroxide label, although the heme triplet state is not directly observable by an electron spin echo.</dcterms:abstract>
    <dc:creator>Hintze, Christian</dc:creator>
    <foaf:homepage rdf:resource="http://localhost:8080/"/>
    <dcterms:issued>2016-06-16</dcterms:issued>
    <dc:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2016-09-09T13:04:03Z</dc:date>
    <dcterms:title>Laser-Induced Magnetic Dipole Spectroscopy</dcterms:title>
    <dc:creator>Drescher, Malte</dc:creator>
    <dcterms:available rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2016-09-09T13:04:03Z</dcterms:available>
    <dc:contributor>Domingo Köhler, Silvia</dc:contributor>
    <dspace:isPartOfCollection rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/29"/>
    <dc:creator>Jeschke, Gunnar</dc:creator>
  </rdf:Description>
</rdf:RDF>
kops.flag.knbibliographytrue
kops.sourcefieldThe Journal of Physical Chemistry Letters. 2016, <b>7</b>(12), pp. 2204-2209. eISSN 1948-7185. Available under: doi: 10.1021/acs.jpclett.6b00765deu
kops.sourcefield.plainThe Journal of Physical Chemistry Letters. 2016, 7(12), pp. 2204-2209. eISSN 1948-7185. Available under: doi: 10.1021/acs.jpclett.6b00765deu
kops.sourcefield.plainThe Journal of Physical Chemistry Letters. 2016, 7(12), pp. 2204-2209. eISSN 1948-7185. Available under: doi: 10.1021/acs.jpclett.6b00765eng
relation.isAuthorOfPublication2b064cbe-4ce3-4ed1-b6ce-a068c6f1506e
relation.isAuthorOfPublication841734af-3681-4738-97fa-51290de2bb47
relation.isAuthorOfPublication2d8db9e8-8b17-4849-8392-946c6bb78d7c
relation.isAuthorOfPublication786195e5-524e-4a1e-ae9d-dd0d3b4e92da
relation.isAuthorOfPublication50c78ea9-293f-4d20-a06a-32f84ce06269
relation.isAuthorOfPublication.latestForDiscovery2b064cbe-4ce3-4ed1-b6ce-a068c6f1506e
source.bibliographicInfo.fromPage2204eng
source.bibliographicInfo.issue12eng
source.bibliographicInfo.toPage2209eng
source.bibliographicInfo.volume7eng
source.identifier.eissn1948-7185eng
source.periodicalTitleThe Journal of Physical Chemistry Letterseng

Dateien