Shifts in peptide and protein charge state distributions with varying spray tip orifice diameter in nanoelectrospray Fourier transform ion cycitron resonance mass spectrometry

被引:51
作者
Li, Y [1 ]
Cole, RB [1 ]
机构
[1] Univ New Orleans, Dept Chem, New Orleans, LA 70148 USA
关键词
D O I
10.1021/ac0301402
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The influence of the diameter of the spray tip employed for nano-electrospray mass spectrometry (nano-ES-MS) upon mass spectral charge state distributions was investigated using angiotensin I (M-r = 1296), insulin (M-r = 5774), and ubiquitin (M-r = 8560) as test analytes. Under a variety of experimental conditions, the charge state distributions of the test peptides and protein consistently shifted toward higher values as the tip orifice diameter decreased. Ibis finding indicates that the use of narrow diameter capillaries can promote the formation of higher charge state ions that are more reactive precursors in tandem mass spectrometry experiments. A detailed comparison of charge state distributions obtained for nanospray capillaries of varying diameters was undertaken while systematically varying experimental parameters such as sample flow rate, analyte concentration, solvent composition, and electrospray current. The general tendency to obtain higher charge states from narrow diameter capillaries was conserved throughout, but tips with smaller orifices were more sensitive to sample flow rate (the average charge state was lowered significantly as flow was raised), whereas tips with bigger,orifices were more sensitive to analyte concentration and pH of the solution (as each was lowered, the average charge state increased).
引用
收藏
页码:5739 / 5746
页数:8
相关论文
共 53 条
[1]  
Amad MH, 2000, J MASS SPECTROM, V35, P784, DOI 10.1002/1096-9888(200007)35:7<784::AID-JMS17>3.0.CO
[2]  
2-Q
[3]   MECHANISM OF PRODUCTION OF IONS IN ELECTROSPRAY MASS-SPECTROMETRY [J].
ASHTON, DS ;
BEDDELL, CR ;
COOPER, DJ ;
GREEN, BN ;
OLIVER, RWA .
ORGANIC MASS SPECTROMETRY, 1993, 28 (06) :721-728
[4]   ACTIVATION-ENERGIES FOR GAS-PHASE DISSOCIATIONS OF MULTIPLY CHARGED IONS FROM ELECTROSPRAY IONIZATION MASS-SPECTROMETRY [J].
BUSMAN, M ;
ROCKWOOD, AL ;
SMITH, RD .
JOURNAL OF PHYSICAL CHEMISTRY, 1992, 96 (06) :2397-2400
[5]   DEPROTONATION REACTIONS OF MULTIPLY PROTONATED UBIQUITIN IONS [J].
CASSADY, CJ ;
WRONKA, J ;
KRUPPA, GH ;
LAUKIEN, FH .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 1994, 8 (05) :394-400
[6]   AN ELECTROSPRAY-IONIZATION MASS-SPECTROMETER WITH NEW FEATURES [J].
CHOWDHURY, SK ;
KATTA, V ;
CHAIT, BT .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 1990, 4 (03) :81-87
[7]   PROBING CONFORMATIONAL-CHANGES IN PROTEINS BY MASS-SPECTROMETRY [J].
CHOWDHURY, SK ;
KATTA, V ;
CHAIT, BT .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1990, 112 (24) :9012-9013
[8]   SOLVENT EFFECT ON ANALYTE CHARGE-STATE, SIGNAL INTENSITY, AND STABILITY IN NEGATIVE-ION ELECTROSPRAY MASS-SPECTROMETRY - IMPLICATIONS FOR THE MECHANISM OF NEGATIVE-ION FORMATION [J].
COLE, RB ;
HARRATA, AK .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1993, 4 (07) :546-556
[9]   CHARGE-STATE DISTRIBUTION AND ELECTRIC-DISCHARGE SUPPRESSION IN NEGATIVE-ION ELECTROSPRAY MASS-SPECTROMETRY USING CHLORINATED SOLVENTS [J].
COLE, RB ;
HARRATA, AK .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 1992, 6 (08) :536-539
[10]  
Covey T R, 1988, Rapid Commun Mass Spectrom, V2, P249, DOI 10.1002/rcm.1290021111