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Electron spin resonance of spin trapped radicals in γ-irradiated polycrystalline dipeptides. Chromatographic separation of radicals

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Polycrystalline dipeptides (glycyl-glycine, glycyl-L-valine, glycyl-L-leucine, L-alanyl-glycine, and L-prolyl-L-alanine) were γ-irradiated at room temperature in the absence of air. Subsequently they were dissolved in aqueous solutions containing 2-methyl-2-nitrosopropane as the spin trap. From the esr spectra of the nitroxide radicals separated by high-performance liquid chromatography, structural assignments of the radicals were made. For glycyl peptides, H-abstraction from the α-carbon atoms of the carboxyl terminal residues and from the side-chains were observed. For L-alanyl-glycine, H-abstraction from the glycyl residue and the formation of the deamination radical could be shown to occur. For L-prolyl-L-alanine, the ring opening (deamination) reaction, decarboxylation and H-abstraction from the C-terminal a-carbon were seen.
Title: Electron spin resonance of spin trapped radicals in γ-irradiated polycrystalline dipeptides. Chromatographic separation of radicals
Description:
Polycrystalline dipeptides (glycyl-glycine, glycyl-L-valine, glycyl-L-leucine, L-alanyl-glycine, and L-prolyl-L-alanine) were γ-irradiated at room temperature in the absence of air.
Subsequently they were dissolved in aqueous solutions containing 2-methyl-2-nitrosopropane as the spin trap.
From the esr spectra of the nitroxide radicals separated by high-performance liquid chromatography, structural assignments of the radicals were made.
For glycyl peptides, H-abstraction from the α-carbon atoms of the carboxyl terminal residues and from the side-chains were observed.
For L-alanyl-glycine, H-abstraction from the glycyl residue and the formation of the deamination radical could be shown to occur.
For L-prolyl-L-alanine, the ring opening (deamination) reaction, decarboxylation and H-abstraction from the C-terminal a-carbon were seen.

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