Internal energy distributions in desorption electrospray ionization (DESI)

被引:80
作者
Nefliu, Marcela [1 ]
Smith, Jonell N. [1 ]
Venter, Andre [1 ]
Cooks, R. Graham [1 ]
机构
[1] Purdue Univ, Dept Chem, W Lafayette, IN 47907 USA
关键词
D O I
10.1016/j.jasms.2007.11.019
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The internal energy distributions of typical ions generated by desorption electrospray ionization (DEST) were measured using the "survival yield" method, and compared with corresponding data for electrospray ionization (EST) and electrosonic spray ionization (ESSI). The results show that the three ionization methods produce populations of ions having internal energy distributions of similar shapes and mean values (1.7-1.9 eV) suggesting similar phenomena, at least in the later stages of the process leading from solvated droplets to gas-phase ions. These data on energetics are consistent with the view that DEST involves "droplet pick-up" (liquid-liquid extraction) followed by ESI-like desolvation and gas-phase ion formation. The effects of various experimental parameters on the degree of fragmentation of p-methoxy-benzylpyridinium ions were compared between DEST and ESSI. The results show similar trends in the survival yields as a function of the nebulizing gas pressure, solvent flow rate, and distance from the sprayer tip to the MS inlet. These observations are consistent with the mechanism noted above and they also enable the user to exercise control over the energetics of the DEST ionization process, through manipulation of external and internal ion source parameters.
引用
收藏
页码:420 / 427
页数:8
相关论文
共 66 条
[1]   Direct high-resolution peptide and protein analysis by desorption electrospray ionization Fourier transform ion cyclotron resonance mass spectrometry [J].
Bereman, Michael S. ;
Nyadong, Leonard ;
Fernandez, Facundo M. ;
Muddiman, David C. .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2006, 20 (22) :3409-3411
[2]   Evaluation of protocols for reproducible electrospray in-source collisionally induced dissociation on various liquid chromatography/mass spectrometry instruments and the development of spectral libraries [J].
Bristow, AWT ;
Nichols, WF ;
Webb, KS ;
Conway, B .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2002, 16 (24) :2374-2386
[3]   SELECTIVE GENERATION OF CHARGE-DEPENDENT - INDEPENDENT ION ENERGY-DISTRIBUTIONS FROM A HEATED CAPILLARY ELECTROSPRAY SOURCE [J].
CAMPBELL, VL ;
GUAN, ZQ ;
LAUDE, DA .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1994, 5 (04) :221-229
[4]   Combining desorption electrospray ionization mass spectrometry and nuclear magnetic resonance for differential metabolomics without sample preparation [J].
Chen, Huanwen ;
Pan, Zhengzheng ;
Talaty, Nari ;
Raftery, Daniel ;
Cooks, R. Graham .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2006, 20 (10) :1577-1584
[5]   Desorption electrospray ionization mass spectrometry for high-throughput analysis of pharmaceutical samples in the ambient environment [J].
Chen, HW ;
Talaty, NN ;
Takáts, Z ;
Cooks, RG .
ANALYTICAL CHEMISTRY, 2005, 77 (21) :6915-6927
[6]  
Collette C, 1998, RAPID COMMUN MASS SP, V12, P1673, DOI 10.1002/(SICI)1097-0231(19981130)12:22<1673::AID-RCM385>3.0.CO
[7]  
2-A
[8]  
Collette C, 1998, RAPID COMMUN MASS SP, V12, P165, DOI 10.1002/(SICI)1097-0231(19980227)12:4<165::AID-RCM140>3.3.CO
[9]  
2-T
[10]   Simulation of atmospheric transport and droplet-thin film collisions in desorption electrospray ionization [J].
Costa, Anthony B. ;
Cooks, R. Graham .
CHEMICAL COMMUNICATIONS, 2007, (38) :3915-3917