The role of the position of the basic residue in the generation and fragmentation of peptide radical cations
Author:
Publisher
Elsevier BV
Subject
Physical and Theoretical Chemistry,Spectroscopy,Condensed Matter Physics,Instrumentation
Reference27 articles.
1. Molecular Radical Cations of Oligopeptides
2. Side-chain radical losses from radical cations allows distinction of leucine and isoleucine residues in the isomeric peptides Gly-XXX-Arg
3. Copper-Mediated Peptide Radical Ions in the Gas Phase
4. Comparing the gas-phase fragmentation reactions of protonated and radical cations of the tripeptides GXR
5. Designing copper(ii) ternary complexes to generate radical cations of peptides in the gas phase: Role of the auxiliary ligand
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1. Tautomerization and Dissociation of Molecular Peptide Radical Cations;The Chemical Record;2017-06-26
2. Nucleophilic substitution by amide nitrogen in the aromatic rings of [zn − H]˙+ ions; the structures of the [b2 − H − 17]˙+ and [c1 − 17]+ ions;Physical Chemistry Chemical Physics;2016
3. α-Radical-induced CO2 loss from the aspartic acid side chain of the collisionally induced tripeptide aspartylglycylarginine radical cation;International Journal of Mass Spectrometry;2015-11
4. Radical-driven peptide backbone dissociation tandem mass spectrometry;Mass Spectrometry Reviews;2014-05-26
5. Hydrogen Bonding Constrains Free Radical Reaction Dynamics at Serine and Threonine Residues in Peptides;The Journal of Physical Chemistry A;2014-03-20
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