Comparison of Functional Group Selective Ion-Molecule Reactions of Trimethyl Borate in Different Ion Trap Mass Spectrometers

被引:20
作者
Habicht, Steve C. [1 ,2 ]
Vinueza, Nelson R. [1 ]
Amundson, Lucas M. [1 ]
Kenttaemaa, Hilkka I. [1 ]
机构
[1] Purdue Univ, Dept Chem, W Lafayette, IN 47906 USA
[2] Ctr Naval Anal, Alexandria, VA 22311 USA
基金
美国国家科学基金会;
关键词
Ion-molecule reactions; Functional groups; FTICR; LQIT; LTQ; CAD; HPLC/MS; PHASE HYDROGEN/DEUTERIUM EXCHANGE; GAS-PHASE; ION/MOLECULE REACTIONS; INDUCED DISSOCIATION; MONOFUNCTIONAL COMPOUNDS; ELECTROSPRAY-IONIZATION; NONCOVALENT COMPLEXES; H/D EXCHANGE; IDENTIFICATION; PEPTIDES;
D O I
10.1007/s13361-010-0050-3
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We report here a comparison of the use of diagnostic ion-molecule reactions for the identification of oxygen-containing functional groups in Fourier-transform ion cyclotron resonance (FTICR) and linear quadrupole ion trap (LQIT) mass spectrometers. The ultimate goal of this research is to be able to identify functionalities in previously unknown analytes by using many different types of mass spectrometers. Previous work has focused on the reactions of various boron reagents with protonated oxygen-containing analytes in FTICR mass spectrometers. By using a LQIT modified to allow the introduction of neutral reagents into the helium buffer gas, this methodology has been successfully implemented to this type of an ion trap instrument. The products obtained from the reactions of trimethyl borate (TMB) with various protonated analytes are compared for the two instruments. Finally, the ability to integrate these reactions into LC-MS experiments on the LQIT is demonstrated.
引用
收藏
页码:520 / 530
页数:11
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