کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1196157 | 964459 | 2006 | 8 صفحه PDF | دانلود رایگان |
We report the electron capture dissociation (ECD) mass spectrometry of the third generation polyamidoamine (PAMAM) dendrimer that contains amide functionalities. The dendrimer was chosen because it offers a unique opportunity to understand the ECD behavior of the amide functionality in a framework other than peptides/proteins. In this study, PAMAM ECD was found to exhibit a fragmentation pattern strikingly different from that of ordinary peptide/protein ECD. Specifically, ECD of multiply protonated PAMAM ions gave rise to significant b
• ,y cleavages as well as S,E dissociations but, unexpectedly, only minor c,z
• fragmentations are observed. In an effort to account for the unexpectedly different fragmentation pattern, a comparative ECD experiment on the poly(propylene imine) dendrimer in which the amide bond moiety is not available and density functional theory calculations (B3LYP/6-311 + G(d)) investigations on the model system of a charge-solvated single-repeat unit were carried out. On the basis of these results, we discuss here possible implications of intramolecular charge-solvation, energy barriers in dissociation reactions, and macromolecular properties of the dendritic molecule for understanding the reaction pathway of PAMAM ECD.
Journal: Journal of the American Society for Mass Spectrometry - Volume 17, Issue 4, April 2006, Pages 536–543