Magdalena Rudowska, Robert Wieczorek, Alicja Kluczyk, Piotr Stefanowicz, Zbigniew Szewczuk
Index: J. Am. Soc. Mass Spectrom. 24 , 846-56, (2013)
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The fragmentation of peptides containing quaternary ammonium group, but lacking easily mobilizable protons, was examined with the aid of deuterium-labeled analogs and quantum-chemical modeling. The fragmentation of oligoproline containing quaternary ammonium group involves the mobilization of hydrogens localized at α- and γ- or δ-carbon atoms in the pyrrolidine ring of proline. The study of the dissociation pattern highlights the unusual proline residue behavior during MS/MS experiments of peptides.
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