Anionic copper complex fragmentations from enkephalins under low-energy collision-induced dissociation in an ion trap mass spectrometer

2004 ◽  
Vol 39 (8) ◽  
pp. 903-912 ◽  
Author(s):  
Anne Bossée ◽  
Carlos Afonso ◽  
Françoise Fournier ◽  
Olivier Tasseau ◽  
Claude Pepe ◽  
...  
Keyword(s):  
Mass Spectrometer ◽  
Copper Complex ◽  
Ion Trap ◽  
Low Energy ◽  
Collision Induced Dissociation ◽  
Energy Collision ◽  
Ion Trap Mass Spectrometer

scholarly journals Evaluation of Front-End Higher Energy Collision-Induced Dissociation on a Benchtop Dual-Pressure Linear Ion Trap Mass Spectrometer for Shotgun Proteomics

2012 ◽  
Vol 84 (3) ◽  
pp. 1533-1539 ◽  
Author(s):  
Michael S. Bereman ◽  
Jesse D. Canterbury ◽  
Jarrett D. Egertson ◽  
Julie Horner ◽  
Philip M. Remes ◽  
...  
Keyword(s):  
Mass Spectrometer ◽  
Ion Trap ◽  
Shotgun Proteomics ◽  
Collision Induced Dissociation ◽  
Linear Ion Trap ◽  
Energy Collision ◽  
Ion Trap Mass Spectrometer ◽  
Front End

Gas Phase Reactions of Trimethylborate with the [M − H]− Ions of Nucleotides and Their Non-Covalent Homo- and Heterodimer Complexes

2003 ◽  
Vol 56 (5) ◽  
pp. 389 ◽  
Author(s):  
Ana K. Vrkic ◽  
Richard A. J. O'Hair
Keyword(s):  
Gas Phase ◽  
Mass Spectrometer ◽  
Ion Trap ◽  
Quadrupole Ion Trap ◽  
Methanol Molecule ◽  
Collision Induced Dissociation ◽  
Base Loss ◽  
Gas Phase Reactions ◽  
Ion Trap Mass Spectrometer ◽  
Neutral Base

Trimethylborate (TMB) reacts with deprotonated monomer, homo-, and heterodimer ions of nucleotides (2′-deoxyadenosine-5′-monophosphate [dAMP], 2′-deoxycytidine-5′-monophosphate [dCMP], 2′-deoxyguanosine-5′-monophosphate [dGMP], and 2′-deoxythymidine-5′-monophosphate [dTMP]) in a quadrupole ion trap mass spectrometer by addition with concomitant elimination of one or two methanol molecules (monomers), one or three methanol molecules (homodimers), and three methanol molecules (heterodimers). The mode of reaction appears to influence the observed rates, with the loss of only one methanol molecule corresponding to the fastest rate. There appears to be a structure–reactivity correlation for the monomers, with the [dGMP – H]– ions (which adopt a syn conformation of the guanine moiety) reacting fastest with TMB through the loss of only one methanol molecule. No such structure–reactivity trends are observed for the homo- and heterodimers. In addition, the collision-induced dissociation (CID) reactions of the [(dXMP)n − H]– (n = 1 or 2) as well as the [dXMP + dYMP – H + (CH3O)3B – 3(CH3OH)]– ions (where nucleotides X, Y = A, C, G, or T) were studied. The latter fragment to form [dXMP – H + BPO4]– and [dXMP – 3H + BPO3]– ions (where X = A, C, G, or T), while [dXMP – H]– ions fragment by neutral base loss. The homo- and heterodimers fragment to form [dXMP – H]– and [dXMP + HPO3]– ions, and the relative abundances of the [dXMP – H]– monomer ions from the heterodimers led to the following acidity order: dGMP ≈ dTMP > dCMP > dAMP.

Collision-Induced Dissociation Studies of Poly(vinylidene) Fluoride Telomers in an Electrospray-Ion Trap Mass Spectrometer

2002 ◽  
Vol 74 (13) ◽  
pp. 3213-3220 ◽  
Author(s):  
A. Marie ◽  
F. Fournier ◽  
J. C. Tabet ◽  
B. Améduri ◽  
J. Walker
Keyword(s):  
Mass Spectrometer ◽  
Vinylidene Fluoride ◽  
Ion Trap ◽  
Collision Induced Dissociation ◽  
Ion Trap Mass Spectrometer ◽  
Poly Vinylidene Fluoride
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