Gas‐phase rearrangement reaction of Schiff‐base‐modified peptide ions. (13th November 2018)
- Record Type:
- Journal Article
- Title:
- Gas‐phase rearrangement reaction of Schiff‐base‐modified peptide ions. (13th November 2018)
- Main Title:
- Gas‐phase rearrangement reaction of Schiff‐base‐modified peptide ions
- Authors:
- Wang, Nan
Pilo, Alice L.
Zhao, Feifei
Bu, Jiexun
McLuckey, Scott A. - Abstract:
- Abstract : Rationale: Schiff base modification of peptides has been shown to facilitate their primary structural characterization via tandem mass spectrometry. However, we have discovered a novel rearrangement reaction via ion trap collisional activation involving the imine of the Schiff base and one of several functional groups, particularly the side chains of the basic residues lysine, arginine, and histidine, in the peptide. Methods: Gas‐phase ion/ion reactions involving an aldehyde‐containing reagent were used to generate Schiff‐base‐modified model peptides in a hybrid triple quadrupole/linear ion trap tandem mass spectrometer. Subsequent ion trap collisional activation was used to study the rearrangement reaction. Results: Schiff‐base‐modified peptide ions were found to undergo a rearrangement reaction that was observed to be either a major or minor contributor to the product ion spectrum, depending upon a variety of factors that include, for example, ion polarity, identity of the nucleophile in the peptide (e.g., side chains of lysine, histidine, and arginine), and the position of the nucleophile relative to the imine. Conclusions: Relatively low‐energy rearrangement reactions can occur in Schiff‐base‐modified peptide ions that involve the imine of the Schiff base and a nucleophile present in the polypeptide. While this rearrangement process does not appear to compromise the structural information that can be generated via collisional activation of Schiff‐base‐modifiedAbstract : Rationale: Schiff base modification of peptides has been shown to facilitate their primary structural characterization via tandem mass spectrometry. However, we have discovered a novel rearrangement reaction via ion trap collisional activation involving the imine of the Schiff base and one of several functional groups, particularly the side chains of the basic residues lysine, arginine, and histidine, in the peptide. Methods: Gas‐phase ion/ion reactions involving an aldehyde‐containing reagent were used to generate Schiff‐base‐modified model peptides in a hybrid triple quadrupole/linear ion trap tandem mass spectrometer. Subsequent ion trap collisional activation was used to study the rearrangement reaction. Results: Schiff‐base‐modified peptide ions were found to undergo a rearrangement reaction that was observed to be either a major or minor contributor to the product ion spectrum, depending upon a variety of factors that include, for example, ion polarity, identity of the nucleophile in the peptide (e.g., side chains of lysine, histidine, and arginine), and the position of the nucleophile relative to the imine. Conclusions: Relatively low‐energy rearrangement reactions can occur in Schiff‐base‐modified peptide ions that involve the imine of the Schiff base and a nucleophile present in the polypeptide. While this rearrangement process does not appear to compromise the structural information that can be generated via collisional activation of Schiff‐base‐modified peptide ions, it can siphon away signal from the structurally diagnostic processes in some instances. … (more)
- Is Part Of:
- Rapid communications in mass spectrometry. Volume 32:Number 24(2018)
- Journal:
- Rapid communications in mass spectrometry
- Issue:
- Volume 32:Number 24(2018)
- Issue Display:
- Volume 32, Issue 24 (2018)
- Year:
- 2018
- Volume:
- 32
- Issue:
- 24
- Issue Sort Value:
- 2018-0032-0024-0000
- Page Start:
- 2166
- Page End:
- 2173
- Publication Date:
- 2018-11-13
- Subjects:
- Mass spectrometry -- Periodicals
543.65 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/rcm.8298 ↗
- Languages:
- English
- ISSNs:
- 0951-4198
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 7254.440000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 8627.xml