Dissociative recombination cross section and branching ratios of protonated dimethyl disulfide and N-methylacetamide

Dimethyl disulfide (DMDS) and N-methylacetamide are two first choice model systems that represent the disulfide bridge bonding and the peptide bonding in proteins. These molecules are therefore suitable for investigation of the mechanisms involved when proteins fragment under electron capture dissoc...

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Veröffentlicht in:The Journal of chemical physics Jg. 121; H. 12; S. 5700
Hauptverfasser: al-Khalili, A, Thomas, R, Ehlerding, A, Hellberg, F, Geppert, W D, Zhaunerchyk, V, af Ugglas, M, Larsson, M, Uggerud, E, Vedde, J, Adlhart, C, Semaniak, J, Kamińska, M, Zubarev, R A, Kjeldsen, F, Andersson, P U, Osterdahl, F, Bednarska, V A, Paál, A
Format: Journal Article
Sprache:Englisch
Veröffentlicht: United States 22.09.2004
ISSN:0021-9606
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Zusammenfassung:Dimethyl disulfide (DMDS) and N-methylacetamide are two first choice model systems that represent the disulfide bridge bonding and the peptide bonding in proteins. These molecules are therefore suitable for investigation of the mechanisms involved when proteins fragment under electron capture dissociation (ECD). The dissociative recombination cross sections for both protonated DMDS and protonated N-methylacetamide were determined at electron energies ranging from 0.001 to 0.3 eV. Also, the branching ratios at 0 eV center-of-mass collision energy were determined. The present results give support for the indirect mechanism of ECD, where free hydrogen atoms produced in the initial fragmentation step induce further decomposition. We suggest that both indirect and direct dissociations play a role in ECD.
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ISSN:0021-9606
DOI:10.1063/1.1782772