Premium
Photodissociation at 193 nm of some singly protonated peptides and proteins with m/z 2000–9000 using a tandem time‐of‐flight mass spectrometer equipped with a second source for delayed extraction/post‐acceleration of product ions
Author(s) -
Moon Jeong Hee,
Shin Young Sik,
Cha Hyun Jung,
Kim Myung Soo
Publication year - 2007
Publication title -
rapid communications in mass spectrometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.528
H-Index - 136
eISSN - 1097-0231
pISSN - 0951-4198
DOI - 10.1002/rcm.2855
Subject(s) - chemistry , protonation , photodissociation , ion , mass spectrometry , tandem mass spectrometry , analytical chemistry (journal) , photochemistry , chromatography , organic chemistry
A tandem time‐of‐flight mass spectrometer was built for photodissociation (PD) of singly protonated peptides and small proteins generated by matrix‐assisted laser desorption/ionization. PD was performed in a second source after deceleration of precursor ions. The delayed extraction/post‐acceleration scheme was used for the product ions. For the PD at 193 nm of small singly protonated peptides, the present instrument showed much better sensitivity and resolution for product ions than the previous one (Moon JH, Yoon SH, Kim MS, Bull. Korean Chem. Soc. 2005; 26: 763) even though the overall spectral patterns obtained with the two instruments were similar. The present instrument was inferior in precursor ion selection and background noise level. PD was achieved for precursor ions as large as the singly protonated ubiquitin ( m/z 8560.63), indicating that the photoexcitation is capable of supplying a sufficient amount of internal energy to dissociate large singly protonated proteins. As the precursor ion m/z increased, however, product ion signals deteriorated rather rapidly. As in the PD of small peptide ions with m/z around 1000, the types of the product ions generated from singly protonated peptides with m/z in the range 2000–4000 were mostly determined by the positions of arginine residues. Namely, a n and d n ions dominated when an arginine residue(s) was near the N‐terminus while v n , w n , x n and y n dominated when the same residue(s) was near the C‐terminus. In addition, d n , v n and w n ions were generated according to the correlation rules previously observed in the collisionally activated dissociation. Isoleucine and leucine isomers could be easily distinguished based on the w n and d n ions. Copyright © 2007 John Wiley & Sons, Ltd.