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Updated: Jun 25, 2026

Proton Transfer and Protein Conformation Dynamics in Photosensitive Proteins by Time-resolved Step-scan Fourier-transform Infrared Spectroscopy
Published on: June 27, 2014
Infrared spectroscopy of fragments from doubly protonated tryptic peptides
Benjamin J Bythell1, Undine Erlekam, Béla Paizs
1Department of Molecular Biophysics, German Cancer Research Center, Im Neuenheimer Feld 580, Heidelberg, Germany.
Abstract:
Most proteins in proteomics are identified from tandem mass spectra of doubly protonated tryptic peptides. Statistical studies indicate that these spectra fall into two distinct classes. IR spectroscopy experiments and DFT calculations performed on model b(2) ions show that peptides producing Class I spectra form protonated oxazolone ions (see figure) and not protonated diketopiperazines as proposed elsewhere.
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