• Medientyp: E-Artikel
  • Titel: Dynorphin A(1–17) biotransformation in striatum of freely moving rats using microdialysis and matrix‐assisted laser desorption/ionization mass spectrometry
  • Beteiligte: Reed, Brian; Zhang, Yong; Chait, Brian T.; Kreek, Mary Jeanne
  • Erschienen: Wiley, 2003
  • Erschienen in: Journal of Neurochemistry, 86 (2003) 4, Seite 815-823
  • Sprache: Englisch
  • DOI: 10.1046/j.1471-4159.2003.01859.x
  • ISSN: 0022-3042; 1471-4159
  • Schlagwörter: Cellular and Molecular Neuroscience ; Biochemistry
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  • Beschreibung: <jats:title>Abstract</jats:title><jats:p>The biotransformation of the opioid peptide dynorphin A(1–17) was investigated in striatum of freely moving Fischer rats, by direct infusion of this peptide, followed by recovery of the resulting biotransformation products via microdialysis and identification using matrix‐assisted laser desorption/ionization mass spectrometry. The observed peptides are consistent with enzymatic cleavage at the Arg<jats:sup>7</jats:sup>‐Ile<jats:sup>8</jats:sup> position of dynorphin A(1–17), followed by terminal degradation of the resulting dynorphin A(1–7) and dynorphin A(8–17) peptides. Unexpectedly, novel post‐translational modifications were found on C‐terminal fragments of dynorphin A(1–17). Using tandem mass spectrometry, a covalent modification of mass 172 Da, the nature of which is not understood, was found on the tryptophan residue of C‐terminal fragments (Trp<jats:sup>14</jats:sup>). Additional modifications, of mass 42 and 113 Da, were also found on the N‐terminus (Ile<jats:sup>8</jats:sup> or Pro<jats:sup>10</jats:sup>) of these same C‐terminal fragments. The role of these modifications of C‐terminal fragments has not yet been characterized.</jats:p>
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