Selective sampling of multiply phosphorylated peptides by capillary electrophoresis for electrospray ionization mass spectrometry analysis

2007 ◽  
Vol 1156 (1-2) ◽  
pp. 101-110 ◽  
Author(s):  
Jennifer N.M. Ballard ◽  
Gilles A. Lajoie ◽  
Ken K.-C. Yeung
Keyword(s):  
Mass Spectrometry ◽  
Capillary Electrophoresis ◽  
Electrospray Ionization ◽  
Electrospray Ionization Mass Spectrometry ◽  
Mass Spectrometry Analysis ◽  
Ionization Mass Spectrometry ◽  
Ionization Mass ◽  
Spectrometry Analysis ◽  
Selective Sampling ◽  
Phosphorylated Peptides

scholarly journals A Non-Covalent Dimer Formation of Quaternary Ammonium Cation with Unusual Charge Neutralization in Electrospray-Ionization Mass Spectrometry

Molecules ◽  
2021 ◽  
Vol 26 (19) ◽  
pp. 5868
Author(s):  
Paulina Grocholska ◽  
Marta Kowalska ◽  
Robert Wieczorek ◽  
Remigiusz Bąchor
Keyword(s):  
Mass Spectrometry ◽  
Electrospray Ionization ◽  
Electrospray Ionization Mass Spectrometry ◽  
Quaternary Ammonium ◽  
Mass Spectrometry Analysis ◽  
Ionization Mass Spectrometry ◽  
Ionization Mass ◽  
Charge Neutralization ◽  
Spectrometry Analysis ◽  
Covalent Dimer

Specific and nonspecific non-covalent molecular association of biomolecules is characteristic for electrospray-ionization mass spectrometry analysis of biomolecules. Understanding the interaction between two associated molecules is of significance not only from the biological point of view but also gas phase analysis by mass spectrometry. Here we reported a formation of non-covalent dimer of quaternary ammonium denatonium cation with +1 charge detected in the positive ion mode electrospray ionization mass spectrometry analysis of denatonium benzoate. Hydrogen deuterium exchange of amide and carbon-bonded hydrogens revealed that charge neutralization of one denatonium cation is the consequence of amide hydrogen dissociation. DFT (Density Functional Theory) calculations proved high thermodynamic stable of formed dimer stabilized by the short and strong N..H-N hydrogen bond. The signal intensity of the peak characterizing non-covalent dimer is low intensity and does not depend on the sample concentration. Additionally, dimer observation was found to be instrument-dependent. The current investigation is the first experimental and theoretical study on the quaternary ammonium ions dimer. Thus the present study has great significance for understanding the structures of the biomolecules as well as materials.

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