|
Title
|
|
|
|
Quantum chemical mass spectrometry: Ab initio study of b₂-ion formation mechanisms for the singly protonated Gln-His-Ser tripeptide
| |
|
Author
|
|
|
|
| |
|
Abstract
|
|
|
|
| Rationale Both amide bond protonation triggering peptide fragmentations and the controversial b(2)-ion structures have been subjects of intense research. The involvement of histidine (H), with its imidazole side chain that induces specific dissociation patterns involving inter-side-chain (ISC) interactions, in b(2)-ion formation was investigated, focusing on the QHS model tripeptide. Methods To identify the effect of histidine on fragmentations issued from ISC interactions, QHS was selected for a comprehensive analysis of the pathways leading to the three possible b(2)-ion structures, using quantum chemical calculations performed at the DFT/B3LYP/6-311+G* level of theory. Electrospray ionization ion trap mass spectrometry allowed the recording of MS2 and MS3 tandem mass spectra, whereas the Quantum Chemical Mass Spectrometry for Materials Science (QCMS(2)) method was used to predict fragmentation patterns. Results Whereas it is very difficult to differentiate among protonated oxazolone, diketopiperazine, or lactam b(2)-ions using MS2 and MS3 mass spectra, the calculations indicated that the QH b(2)-ion (detected at m/z 266) is probably a mixture of the lactam and oxazolone structures formed after amide nitrogen protonation, making the formation of diketopiperazine less likely as it requires an additional step for its formation. Conclusions In contrast to glycine-histidine-containing b(2)-ions, known to be issued from the backbone-imidazole cyclization, we found that interactions between the side chains were not obvious to perceive, neither from a thermodynamics nor from a fragmentation perspective, emphasizing the importance of the whole sequence on the dissociation behavior usually demonstrated from simple glycine-containing tripeptides. |
| |
|
Language
|
|
|
|
English
| |
|
Source (journal)
|
|
|
|
Rapid communications in mass spectrometry. - London
| |
|
Publication
|
|
|
|
London
:
2020
| |
|
ISSN
|
|
|
|
0951-4198
| |
|
DOI
|
|
|
|
10.1002/RCM.8778
| |
|
Volume/pages
|
|
|
|
34
:12
(2020)
, p. 1-13
| |
|
Article Reference
|
|
|
|
UNSP e8778
| |
|
ISI
|
|
|
|
000537149300001
| |
|
Pubmed ID
|
|
|
|
32144813
| |
|
Medium
|
|
|
|
E-only publicatie
| |
|
Full text (Publisher's DOI)
|
|
|
|
| |
|
Full text (publisher's version - intranet only)
|
|
|
|
| |
|