Photodissociation of protonated leucine-enkephalin in the VUV range of 8-40 eV

dc.contributor.authorBari, S.
dc.contributor.authorGonzalez-Magana, O.
dc.contributor.authorReitsma, G.
dc.contributor.authorWerner, J.
dc.contributor.authorSchippers, Stefan
dc.contributor.authorHoekstra, R.
dc.contributor.authorSchlatholter, T.
dc.date.accessioned2023-06-02T13:37:39Z
dc.date.available2012-02-24T08:48:56Z
dc.date.available2023-06-02T13:37:39Z
dc.date.issued2011
dc.description.abstractUntil now, photodissociation studies on free complex protonated peptides were limited to the UV wavelength range accessible by intense lasers. We have studied photodissociation of gas-phase protonated leucine-enkephalin cations for vacuum ultraviolet (VUV) photons energies ranging from 8 to 40 eV. We report time-of-flight mass spectra of the photofragments and various photofragment-yields as a function of photon energy. For sub-ionization energies our results are in line with existing studies on UV photodissociation of leucine-enkephalin. For photon energies exceeding 10 eV we could identify a new dissociation scheme in which photoabsorption leads to a fast loss of the tyrosine side chain. This loss process leads to the formation of a residual peptide that is remarkably cold internally.en
dc.identifier.urihttp://nbn-resolving.de/urn:nbn:de:hebis:26-opus-86319
dc.identifier.urihttps://jlupub.ub.uni-giessen.de//handle/jlupub/16377
dc.identifier.urihttp://dx.doi.org/10.22029/jlupub-15757
dc.language.isoende_DE
dc.rightsIn Copyright*
dc.rights.urihttp://rightsstatements.org/page/InC/1.0/*
dc.subjectphotodissociationen
dc.subjectgas-phase protonated leucine-enkephalin cations tyrosine side chain lossen
dc.subject.ddcddc:530de_DE
dc.titlePhotodissociation of protonated leucine-enkephalin in the VUV range of 8-40 eVen
dc.typearticlede_DE
local.affiliationFB 07 - Mathematik und Informatik, Physik, Geographiede_DE
local.commentDieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG geförderten) Allianz- bzw. Nationallizenz frei zugänglich. This publication is with permission of the rights owner freely accessible due to an Alliance licence and a national licence (funded by the DFG, German Research Foundation) respectively.
local.opus.fachgebietPhysikde_DE
local.opus.id8631
local.opus.instituteInstitut für Atom- und Molekülphysikde_DE
local.source.freetextJournal of Chemical Physics, 2011, 134(2), Article 024314; doi:10.1063/1.3515301de_DE
local.source.urihttps://doi.org/10.1063/1.3515301

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