Analysis of native amino acids by liquid chromatography/electrospray ionization mass spectrometry: comparative study between two sources and interfaces

被引:39
作者
de Person, Marine [1 ]
Chairnbault, Patrick [1 ]
Elfakir, Claire [1 ]
机构
[1] Univ Orleans, CNRS, UMR 6005, ICOA,FR 2708, F-45067 Orleans 2, France
来源
JOURNAL OF MASS SPECTROMETRY | 2008年 / 43卷 / 02期
关键词
amino acids; ion-pair chromatography; electrospray mass spectrometry;
D O I
10.1002/jms.1287
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The analytical performances of two triple-quadrupole instruments, which differ in their atmospheric-pressure sources, were evaluated for native amino acid analysis. The Applied Biosystems/Sciex API 300 instrument was equipped with a turboIon Spray source and a curtain gas interface while the Waters/Micromass Quattro Ultima instrument was characterized by its Z-spray source. Liquid chromatography/mass spectrometry analysis of native amino acids requires volatile ion-pairing mobile phase additives (mainly perfluorinated carboxylic acids). The effects of the structure and concentration of the ion-pairing reagents as well as the organic modifier percentage on the electrospray response of amino acids were studied in detail. The most favourable chromatographic conditions depend strongly on the mass spectrometer used. Several instrumental parameters were also studied, including spray voltage, transmission lens voltages, temperature of desolvation and auxiliary gas flow rates. The results show substantial qualitative differences depending on the instrument geometry. The quantitative performances of the two triple-quadrupole mass spectrometers were evaluated in terms of limits of detection and quantification. The effects of the matrix on the analyte ionization were also examined, and the long-term stability of the electrospray performance was studied over 12 h using a mobile phase containing the perfluorinated ion-pairing reagents. The study provides information on the robustness of the MS instrument and its detection sensitivity towards native amino acid analysis. It appears that each instrument has its good and bad points since one provides higher sensitivity while another is more robust. Copyright (c) 2007 John Wiley & Sons, Ltd.
引用
收藏
页码:204 / 215
页数:12
相关论文
共 23 条
[1]   Determination of 20 underivatized proteinic amino acids by ion-pairing chromatography and pneumatically assisted electrospray mass spectrometry [J].
Chaimbault, P ;
Petritis, K ;
Elfakir, C ;
Dreux, M .
JOURNAL OF CHROMATOGRAPHY A, 1999, 855 (01) :191-202
[2]   Ion-pair chromatography on a porous graphitic carbon stationary phase for the analysis of twenty underivatized protein amino acids [J].
Chaimbault, P ;
Petritis, K ;
Elfakir, C ;
Dreux, M .
JOURNAL OF CHROMATOGRAPHY A, 2000, 870 (1-2) :245-254
[3]   Study of selenium distribution in the protein fractions of the Brazil nut, Bertholletia excelsa [J].
Chunhieng, T ;
Pétritis, K ;
Elfakir, C ;
Brochier, J ;
Goli, T ;
Montet, D .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2004, 52 (13) :4318-4322
[4]   Analysis of native amino acid and peptide enantiomers by high-performance liquid chromatography/atmospheric pressure chemical ionization mass spectrometry [J].
Desai, MJ ;
Armstrong, DW .
JOURNAL OF MASS SPECTROMETRY, 2004, 39 (02) :177-187
[5]   Studies of signal suppression in liquid chromatography-electrospray ionization mass spectrometry using volatile ion-pairing reagents [J].
Gustavsson, SA ;
Samskog, J ;
Markides, KE ;
Långström, B .
JOURNAL OF CHROMATOGRAPHY A, 2001, 937 (1-2) :41-47
[6]  
Hiraoka K, 1995, J Mass Spectrom Soc Jpn, V43, P127, DOI DOI 10.5702/MASSSPEC.43.127
[7]  
HOKAPEK M, 2004, J MASS SPECTROM, V39, P43
[8]   Analysis of underivatized amino acid mixtures using high performance liquid chromatography/dual oscillating nebulizer atmospheric pressure microwave induced plasma ionization-mass spectrometry [J].
Kwon, JY ;
Moini, M .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 2001, 12 (01) :117-122
[9]  
Mansoori BA, 1997, RAPID COMMUN MASS SP, V11, P1120, DOI 10.1002/(SICI)1097-0231(19970630)11:10<1120::AID-RCM976>3.3.CO
[10]  
2-H