Inverse hydrogen migration in arginine-containing peptide ions upon electron transfer
| Autor: | Subhasis Panja, František Tureček, Preben Hvelplund, Steen Brøndsted Nielsen |
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| Rok vydání: | 2008 |
| Předmět: |
Models
Molecular Spectrometry Mass Electrospray Ionization Stereochemistry Radical Static Electricity Protonation Arginine 010402 general chemistry 01 natural sciences Electron Transport chemistry.chemical_compound Electron transfer Structural Biology 0103 physical sciences Guanidine Conformational isomerism Spectroscopy Bond cleavage Molecular Structure 010304 chemical physics Electron-capture dissociation Dipeptides Hydrogen atom 0104 chemical sciences Crystallography chemistry Hydrogen |
| Zdroj: | Panja, S, Nielsen, S B, Hvelplund, P & Turecek, F 2008, ' Inverse Hydrogen Migration in Arginine-Containing Peptide Ions upon Electron Transfer ', Journal of The American Society for Mass Spectrometry, vol. 19, pp. 1726-1742 . https://doi.org/10.1016/j.jasms.2008.08.001 |
| ISSN: | 1044-0305 |
| Popis: | Collisional electron transfer from gaseous Cs atoms was studied for singly and doubly protonated peptides Gly-Arg (GR) and Ala-Arg (AR) at 50- and 100-keV kinetic energies. Singly protonated GR and AR were discharged to radicals that in part rearranged by migration of a C(alpha) hydrogen atom onto the guanidine group. The C(alpha)-radical isomers formed were detected as stable anions following transfer of a second electron. In addition to the stabilizing rearrangements, the radicals underwent side-chain and backbone dissociations. The latter formed z fragments that were detected as the corresponding anions. Analysis of the (GR + H)(.) radical potential energy surface using electronic structure theory in combination with Rice-Ramsperger-Kassel-Marcus calculations of rate constants indicated that the arginine C(alpha) hydrogen atom was likely to be transferred to the arginine side-chain on the experimental timescale ofor=200 ns. Transfer of the Gly C(alpha)H was calculated to have a higher transition-state energy and was not kinetically competitive. Collisional electron transfer to doubly protonated GR and AR resulted in complete dissociation of (GR + 2H)(+.) and (AR + 2H)(+.) ions by loss of H, ammonia, and NC(alpha) bond cleavage. Electronic structure theory analysis of (GR + 2H)(+.) indicated the presence of multiple conformers and electronic states that differed in reactivity and steered the dissociations to distinct channels. Electron attachment to (GR + 2H)(2+) resulted in the formation of closely spaced electronic states of (GR + 2H)(+.) in which the electron density was delocalized over the guanidinium, ammonium, amide, and carboxyl groups. The different behavior of (GR + H)(.) and (GR + 2H)(+.) is explained by the different timescales for dissociation and different internal energies acquired upon electron transfer. |
| Databáze: | OpenAIRE |
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