Ultraviolet photodissociation at 266 nm of phosphorylated peptide cations

• Published in: Rapid communications in mass spectrometry 2009-12, Vol.23 (23), p.3609-3620
• Main Authors: Park, Soojin, Ahn, Wha-Keun, Lee, Sunyoung, Han, Sang Yun, Rhee, Bum Ku, Oh, Han Bin
• Format: Article
• Language: English
• Subjects: Cations - chemistry; Mass Spectrometry - methods; Phosphopeptides - chemistry; Phosphoserine - chemistry; Phosphotyrosine - chemistry; Photochemical Processes; Spectroscopy, Fourier Transform Infrared - methods; Ultraviolet Rays
• ISSN: 0951-4198; 1097-0231; 1097-0231
• DOI: 10.1002/rcm.4184

Ultraviolet (UV) photodissociation (PD) experiments using 266 nm light were performed for a series of phosphopeptide cations in a Fourier transform mass spectrometer. The objective of the experiments was to determine whether 266 nm UV irradiation on the phosphopeptide cations would induce unique peptide backbone dissociation. In addition, the general behavior of the phosphate loss (−80 or −98 Da) was monitored, particularly for those phosphopeptides with a phosphotyrosine residue that itself is a UV chromophore. For phosphopeptides with a UV chromophore, their photodissociation behavior was very similar to that of low‐energy sustained off‐resonance irradiation collisionally activated dissociation (SORI‐CAD), with a few exceptions. For example, b‐ and y‐type peptide backbone fragments were prevalent, and their dephosphorylation behavior was consistent with that of the SORI‐CAD results. For phosphoserine peptides, the loss of a phosphate group was always observed. On the other hand, for phosphotyrosine peptides, the phosphate loss was found to be dependent on the presence of a basic amino group in the sequence and the charge state of the precursor ions, in agreement with the CAD results in the literature. However, hydrogen atom loss or aromatic side chain loss, which is known to be the excited state specific fragmentation pathway, was rarely observed in our 266 nm UV PD experiments, in contrast to the previous UV PD literature (particularly at 220 nm). The mechanism for these observations is described in terms of dominant internal conversion followed by intramolecular vibrational energy redistribution (IVR). Copyright © 2009 John Wiley & Sons, Ltd.